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846 Cards in this Set

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What is the key workup when a patient presents with:

30yo F has wrist pain and a black eye after tripping, falling, and hitting her head on the edge of a table. She looks anxious and give an inconsistent story
- XR - wrist
- CT - head
- Urine toxicology
What are the key elements of the patient history when a patient presents with abuse?
- Establish confidentiality; directly question about physical, sexual, or emotional abuse and about fear, safety, backup plan
- History of frequent accidents/injuries, mental illness, drug use
- Firearms in the home
What are the key elements of the patient physical when a patient presents with abuse?
- Vital signs
- Complete exam +/- pelvic
What is the key differential when a patient presents with:

- 30yo F presents with wrist pain and a sensation of numbness and burning in her palm and the first, second and third fingers of her right hand. The pain worsens at night and is relieved by loose shaking of the hand. There is sensory loss in the same fingers. Exam reveals a positive Tinel's sign.
- Carpal tunnel syndrome
- Median nerve compression in forearm or arm
- Radiculopathy of nerve roots C6 & C7 in cervical spine
What is the key workup when a patient presents with:

- 30yo F presents with wrist pain and a sensation of numbness and burning in her palm and the first, second and third fingers of her right hand. The pain worsens at night and is relieved by loose shaking of the hand. There is sensory loss in the same fingers. Exam reveals a positive Tinel's sign.
- Nerve conduction study
- EMG
What is the key differential when a patient presents with:

- 28 yo F presents with pain in the interphalangeal joints of her hands together with hair loss and a butterfly rash on her face.
- Systemic lupus erythematosus (SLE)
- Rheumatoid arthritis
- Psoriatic arthritis
- Parvovirus B19 infection
What is the key workup when a patient presents with:

- 28 yo F presents with pain in the interphalangeal joints of her hands together with hair loss and a butterfly rash on her face.
- ANA, anti-dsDNA, ESR, C3, C4, rheumatoid factor (RF), CBC
- XR - hands
- UA
What is the key differential when a patient presents with:

- 28 yo F presents with pain in the matacarpophalangeal joints of both hands. Her left knee is also painful and red. She has morning joint stiffness that lasts for an hour. Her mother had rheumatoid arthritis.
- Rheumatoid arthritis
- SLE
- Disseminated gonorrhea
- Arthritis associated with inflammatory bowel disease
- Osteoarthritis
What is the key differential when a patient presents with:

- 28 yo F presents with pain in the matacarpophalangeal joints of both hands. Her left knee is also painful and red. She has morning joint stiffness that lasts for an hour. Her mother had rheumatoid arthritis.
- ANA, anti-dsDNA, ESR, RF, CBC
- XR - hands, left knee
- Cervical culture
- Arthrocentesis & synovial fluid analysis
What is the key differential when a patient presents with:

18yo M presents with pin in the interphalangeal joins of both hands. He also has scaly, salmon-pink lesions on the extensor surface of his elbows and knees.
- Psoriatic arthritis
- Rheumatoid arthritis
- SLE
What is the key workup when a patient presents with:

18yo M presents with pin in the interphalangeal joins of both hands. He also has scaly, salmon-pink lesions on the extensor surface of his elbows and knees.
- RF, ANA, ESR
- CBC
- XR - hands
- XR - pelvis/sacroiliac joints
- Uric acid
What is the key differential when a patient presents with:

65yo F presents with inability to use her left leg and bear weight on it after tripping on a carpet. Onset of menopause was 20 years ago and she did not receive HRT or calcium supplements. her left leg is externally rotated, shortened, and adducted, and there is tenderness in her left groin.
- Hip fracture
- Hip dislocation
- Pelvic fracture
What is the key workup when a patient presents with:

65yo F presents with inability to use her left leg and bear weight on it after tripping on a carpet. Onset of menopause was 20 years ago and she did not receive HRT or calcium supplements. her left leg is externally rotated, shortened, and adducted, and there is tenderness in her left groin.
- XR - hip/pelvis
- CT or MRI - hip
- CBC
- Serum calcium & Vit. D
- Bone density scan (DEXA)
What is the key differential when a patient presents with:

40yo M presents with pain in the right groin after a motor vehicle accident. His right leg is flexed at the hip. adducted, and internally rotated.
- Hip dislocation - traumatic
- Hip fracture
What is the key workup when a patient presents with:

40yo M presents with pain in the right groin after a motor vehicle accident. His right leg is flexed at the hip. adducted, and internally rotated.
- XR - hip
- CT or MRI - hip
- CBC
- PT/PTT
- Blood type & cross match
- Urine toxicology and blood alcohol level
What are the key elements of patient history when a patient presents with low back pain?
- Location, quality, intensity, radiation
- Context: moving furniture, bending/twisting, trauma
- Timing: disturbs sleep
- Associated symptoms: especially constitutional, incontinence
- Exacerbating & alleviating factors
- History of cancer
- Recurrent UTIs, diabetes, renal stones, IV drug use, smoking
What are the key elements of patient physical when a patient presents with low back pain?
- Vital signs, neurologic exam (esp. L4-S1 nerve roots)
- Back palpation & range of motion
- Hip exam
- Rectal exam
What are the key elements of patient history when a patient presents with a child with fever?
- Severity, duration
- Associated localizing symptoms
- Appetite
- Rash
- Sick contacts
- Day care
- Immunizations
- Past history
What are the key elements of patient history when a patient physical with a child with fever?
- Vital signs
- HEENT
- Neck
- Heart & Lungs
- Abdominal
- Skin exam
What are the key elements of patient history when a patient presents with a child with behavioral problems?
- Onset
- Severity
- Duration
- Triggers
- Physical violence or use of weapons
- Substance use
- Developmental history
- Changes in environment/school performance
What are the key elements of patient physical when a patient presents with a child with behavioral problems?
- Vital signs
- Neurological exam
What is the key differential in a patient that presents with:

56yo obese F presents with right knee stiffness and pain that increases with movement. Her symptoms have gradually worsened over the past 10 years. She noticed swelling and deformity of the joint and is having difficulty walking.
- Osteoarthritis
- Pseudogout
- Gout
- Meniscal or ligament damage
What is the key workup in a patient that presents with:

56yo obese F presents with right knee stiffness and pain that increases with movement. Her symptoms have gradually worsened over the past 10 years. She noticed swelling and deformity of the joint and is having difficulty walking.
- XR - knee
- CBC
- ESR
- Knee arthrocentesis & synovial fluid analysis: cell count, Gram stain, culture, crystals)
- MRI - knee
What is the key differential when a patient presents with:

45yo M presents with right knee pain with swelling and redness.
- Septic arthritis
- Gout
- Pseudogout
- Lyme arthritis
- Trauma
- Reiter's arthritis
What is the key workup when a patient presents with:

45yo M presents with right knee pain with swelling and redness.
- CBC
- Knee arthrocentesis and synovial fluid analysis (cell count, gram stain, culture, crystals)
- Blood, urethral cultures
- XR - knee
- Uric acid
- Lyme antibody
What is the key differential when a patient presents with:

65yo M presents with right foot pain. He has been training for a marathon.
- Stress fracture
- Plantar fasciitis
- Foot sprain or strain
What is the key workup when a patient presents with:

65yo M presents with right foot pain. He has been training for a marathon.
- XR - foot
- Bone scan - foot
- MRI - foot
What is the key differential when a patient presents with:

65yo M presents with pain in the heel of the right foot that is most notable with his first few steps and then improves as he continues walking. He has no known trauma.
- Plantar fasciitis
- Heel fracture
- Splinter/foreign body
What is the key workup when a patient presents with:

65yo M presents with pain in the heel of the right foot that is most notable with his first few steps and then improves as he continues walking. He has no known trauma.
- XR - heel
- Bone scan
What is the key differential when a patient presents with:

55yo M presents with pain in the elbow when he plays tennis. His grip is impaired as a result of the pain. There is tenderness over the lateral epicondyle as well as pain on resisted wrist dorsiflexion (Cozen's test) with the elbow in extension.
- Tennis elbow (lateral epicondylitis)
- Stress fracture
What is the key workup when a patient presents with:

55yo M presents with pain in the elbow when he plays tennis. His grip is impaired as a result of the pain. There is tenderness over the lateral epicondyle as well as pain on resisted wrist dorsiflexion (Cozen's test) with the elbow in extension.
- XR - arm
- Bone scan
- MRI - elbow
What is the key differential when a patient presents with:

27yo F presents with painful wrists and elbows, a swollen and hot knee joint that is painful on flexion, a rash on her limbs, and vaginal discharge. She is sexually active with multiple partners and occasionally uses condoms.
- Disseminated gonorrhea
- Rheumatoid arthritis
- SLE
- Psoriatic arthritis
- Reiter's arthritis
What is the key differential when a patient presents with:

27yo F presents with painful wrists and elbows, a swollen and hot knee joint that is painful on flexion, a rash on her limbs, and vaginal discharge. She is sexually active with multiple partners and occasionally uses condoms.
- Knee arthrocentesis & synovial fluid analysis (cell count, Gram stain, culture)
- ANA, anti-dsDNA, ESR, RF, CBC
- Blood, cervical cultures
- XR - knee
What is the key differential when a patient presents with:

60yo F presents with pain in both legs that is induced by walking and is relieved by rest. She had cardiac bypass surgery 6 months ago & continues to smoke heavily.
- Peripheral vascular disease (intermittent claudication)
- Leriche's syndrome (aortoiliac occlusive disease)
- Lumbar spinal stenosis (pseudoclaudication)
- Osteoarthritis
What is the key workup when a patient presents with:

60yo F presents with pain in both legs that is induced by walking and is relieved by rest. She had cardiac bypass surgery 6 months ago & continues to smoke heavily.
- Ankle-brachial index
- Doppler U/S - lower extremity
- Angiography
- MRI - lumbar spine
What is the key differential when a patient presents with:

45yo F presents with right calf pain. Her calf is tender, warm, red, and swollen compared to the left side. She was started on OCPs 2 months ago for dysfunctional uterine bleeding.
- DVT
- Baker's cyst rupture
- Myositis
- Cellulitis
- Superficial venous thrombosis
What is the key workup when a patient presents with:

45yo F presents with right calf pain. Her calf is tender, warm, red, and swollen compared to the left side. She was started on OCPs 2 months ago for dysfunctional uterine bleeding
- Doppler U/S - right leg
- CBC
- CPK
- D-dimer
- PT, aPTT, fibrinogen
- XR - right leg
What is the key differential when a patient presents with:

60yo F c/o left arm pain that started while she was swimming and was relieved by rest.
- Angina/MI
- Tendonitis
- Osteoarthritis
- Shoulder dislocation
What is the key workup when a patient presents with:

60yo F c/o left arm pain that started while she was swimming and was relieved by rest.
- CPK-MB, troponin, ECG
- CBC
- ESR
- XR - shoulder
- CXR
- Echocardiography
- Stress test
What is the key differential when a patient presents with:

50yo M presents with right shoulder pain after falling onto his outstretched hand while skiing. He noticed deformity of his shoulder and had to hold his right arm.
- Shoulder dislocation
- Fracture of the humerus
- Rotator cuff injury
What is the key workup when a patient presents with:

50yo M presents with right shoulder pain after falling onto his outstretched hand while skiing. He noticed deformity of his shoulder and had to hold his right arm.
- XR - shoulder
- XR - arm
- MRI - shoulder
What is the key differential when a patient presents with:

55yo M presents with crampy bilateral thigh & calf pain, fatigue, and dark urine. He is on simvastatin and clofibrate for hyperlipidemia.
- Rhabdomyolysis due to simvastatin or clofibrate
- Polymyositis
- Inclusion body myositis
- Thyroid disease
What is the key workup when a patient presents with:

55yo M presents with crampy bilateral thigh & calf pain, fatigue, and dark urine. He is on simvastatin and clofibrate for hyperlipidemia.
- CBC
- CPK
- Aldolase
- UA
- Urine myoglobin
- TSH
What is the key differential when a patient presents with:

45yo F presents with low back pain that radiates to the lateral aspect of her left foot. Straight leg raising is positive. The patient is unable to tiptoe.
- Disk herniation
- Lumbar muscle strain
- Tumor in the vertebral canal
What is the key workup when a patient presents with:

45yo F presents with low back pain that radiates to the lateral aspect of her left foot. Straight leg raising is positive. The patient is unable to tiptoe.
- XR - L-spine
- MRI - L-spine
What is the key differential when a patient presents with:

45yo F presents with low back pain that started after she cleaned her house. The pain does not radiate, & there is no sensory deficit or weakness in her legs. Paraspinal muscle tenderness and spasm are also noted.
- Lumbar muscle strain
- Disk herniation
- Abdominal aortic aneurysm
- Vertebral compression fracture
What is the key workup when a patient presents with:

45yo F presents with low back pain that started after she cleaned her house. The pain does not radiate, & there is no sensory deficit or weakness in her legs. Paraspinal muscle tenderness and spasm are also noted.
- XR - L-spine
What is the key differential when a patient presents with:

45yo M presents with pain in the lower back and legs during prolonged standing and walking. The pain is relieved by sitting and leaning forward (e.g. pushing a grocery cart).
- Lumbar spinal stenosis
- Lumbar muscle strain
- Tumor in the vertebral canal
- Peripheral vascular disease
What is the key workup when a patient presents with:

45yo M presents with pain in the lower back and legs during prolonged standing and walking. The pain is relieved by sitting and leaning forward (e.g. pushing a grocery cart).
XR - L-spine
MRI - L-spine (preferred)
CT - L-spine
Ankle-brachial index
What is the key differential when a patient presents with:

17yo M presents with low back pain that radiates to the left leg and began after he fell on his knee during gym class. He also describes areas of loss of sensation in his left foot. The pain and sensory loss do not match any known distribution. He insists on requesting a week off from school because of his injury.
- Malingering
- Lumbar muscle strain
- Disk herniation
- Knee or leg fracture
- Ankylosing spondylitis
What is the key workup when a patient presents with:

17yo M presents with low back pain that radiates to the left leg and began after he fell on his knee during gym class. He also describes areas of loss of sensation in his left foot. The pain and sensory loss do not match any known distribution. He insists on requesting a week off from school because of his injury.
- XR - L-spine/knee
- MRI - L-spine
What is the key differential when a patient presents with:

20-day old M presents with fever, decreased breast/feeding, and lethargy. He was born at 36 weeks as a result of premature rupture of membranes.
- Neonatal sepsis
- Meningitis
- Pneumonia
- UTI
What is the key workup when a patient presents with:

20-day old M presents with fever, decreased breast/feeding, and lethargy. He was born at 36 weeks as a result of premature rupture of membranes.
- Physical exam
- CBC, electrolytes
- UA
- Urine culture
- Blood culture
- CXR
- LP - CSF analysis
What is the key differential when a patient presents with:

3yo M presents with a 2-day history of fever and pulling on his right ear. He is otherwise healthy, and his immunizations are up to date. His older sister recently had a cold. The child attends a day care center.
- Acute otitis media
- URI
- Meningitis
- UTI
What is the key workup when a patient presents with:

3yo M presents with a 2-day history of fever and pulling on his right ear. He is otherwise healthy, and his immunizations are up to date. His older sister recently had a cold. The child attends a day care center.
- Physical exam (including pneumatic otoscopy)
- CBC
- UA
What is the key differential when a patient presents with:

12-month-old M presents with fever for the last 2 days accompanied by maculopapular rash on his face and body. He has not yet received the MMR vaccine.
- Measles (or other viral exanthem)
- Rubella
- Roseola
- 5th disease
- Varicella
- Scarlet fever
- Meningitis
What is the key workup when a patient presents with:

12-month-old M presents with fever for the last 2 days accompanied by maculopapular rash on his face and body. He has not yet received the MMR vaccine.
- Physical exam
- CBC
- Viral antibodies/titers
- Throat swab for culture
- LP
What is the key differential when a patient presents with:

4yo M presents with diarrhea, vomiting, lethargy, weakness, and fever. The child attends a day care center where several children have had similar symptoms.
- Gastroenteritis (viral, bacterial, parasitic)
- Food poisoning
- UTI
- URI
- Volvulus
- Intussusception
What is the key workup when a patient presents with:

4yo M presents with diarrhea, vomiting, lethargy, weakness, and fever. The child attends a day care center where several children have had similar symptoms.
- Physical exam
- Stool exam & culture
- CBC
- Electrolytes
- UA, urine culture
- AXR
What is the key differential when a patient presents with:

9yo M presents with a 2-year hisotry of angry outbursts both in school and at home. His mother complains that he runs around "as if driven by a motor". His techer reports that he cannot sit still in class, regularly interrupts his classmates, and has trouble making friends.
- Attention-deficit hyperactivity disorder (ADHD)
- Oppositional defiant disorder
- Manic episode
- Conduct disorder
What is the key workup when a patient presents with:

9yo M presents with a 2-year hisotry of angry outbursts both in school and at home. His mother complains that he runs around "as if driven by a motor". His techer reports that he cannot sit still in class, regularly interrupts his classmates, and has trouble making friends.
- Physical exam
- Mental status exam
What is the key differential when a patient presents with:

12yo F presents with a 2-month history of fighting in school, truancy, and breaking curfew. Her parents recently divorced, and she just started school in a new district. Before her parents divorced, she was an average student with no behavioral problems.
- Adjustment disorder
- Substance intoxication/abuse/dependence
- Manic episode
- Oppositional defiant disorder
- Conduct disorder
What is the key workup when a patient presents with:

12yo F presents with a 2-month history of fighting in school, truancy, and breaking curfew. Her parents recently divorced, and she just started school in a new district. Before her parents divorced, she was an average student with no behavioral problems.
- Physical exam
- Mental status exam
- Urine toxicology
What is the key differential when a patient presents with:

15yo M presents with a 1-year history of failing grades, school absenteeism, and legal problems, including shoplifting. His parents report that he spends most of his time alone in his room, adding that when he does go out, it is with a new set of friends.
- Substance abuse
- Conduct disorder
- Oppositional defiant disorder
- Adjustment disorder
What is the key workup when a patient presents with:

15yo M presents with a 1-year history of failing grades, school absenteeism, and legal problems, including shoplifting. His parents report that he spends most of his time alone in his room, adding that when he does go out, it is with a new set of friends.
- Urine toxicology
- Mental status exam
What is the key differential when a patient presents with:

5yo M presents with 6-month history of temper tantrums that last 5-10 minutes and immediately follow a disappointment or a discipline. He has no trouble sleeping, has had no change in appetite, and does not display these behaviors when he is at day care.
- Age-appropriate behavior
- ADHD
- Oppositional defiant disorder
What is the key workup when a patient presents with:

5yo M presents with 6-month history of temper tantrums that last 5-10 minutes and immediately follow a disappointment or a discipline. He has no trouble sleeping, has had no change in appetite, and does not display these behaviors when he is at day care.
- Physical exam
- Mental status
Which hep virus is a circular, partially double-stranded DNA virus?
Hep B
What is the incubation period & route of transmission for Hep B?
- Incubation: 1-6m
- Transmission: parenteral, sexual, perinatal
What are the 2 markers of HBV infection?
- HBsAg
- IgG anti-HBc Ab
What hep virus is ss(+) RNA virus?
HCV
What is the incubation period & route of transmission for HCV?
- 15-150 days
- Parenteral, Sexual, Perinatal
What Hep virus is incomplete RNA and requires co-infection or superinfects with HBV?
HDV (Deltaviridae)
Where is HDV usually contracted?
- Amazon Basin
- Central Africa
- Mediterranean Basin
- Middle East
What is the difference in diagnosis between and HDV co-infection with HBV & a superinfection (also with HBV)?
Co-infection: IgM anti-HBc Ab (+)
Superinfection: IgM anti-HBc Ab (-)
Which Hep virus has recent be found in solid organ-transplant recipients?
HEV
Which Hep viruses require more than symptomatic therapy?
- Hep B - IF infection is severe
- Hep C - (PEG)INF-alpha
- Hep D - Vaccination against HBV

i.e. Hep A & E are symptomatic only
Which Hep is especially dangerous for pregnant women?
Hep E
What are the extrahepatic manifestations of HBV infection?
- Polyarteritis nodosa
- Glomerulonephritis
- Cryogobulinemia
What are the extrahepatic manifestations of HCV infection?
- Glomerulonephritis
- Cryogobulinemia
- Idiopathic thrombocytopenia purpura
- Lichen Planus
- Raynaud syndrome
- Sjogren's syndrome
- Porphyria cutanea tarda
- Necrotizing cutaneous vasculitis
- Non-Hodgkin's lymphoma
What is the DOC for chronic Hep B?
interferon (W/O ribavirin)
What is the 2nd choice treatment for Hep B?
Choose an oral analog:
- Lamivudine
- Adefovir
- Entecavir
- Tenofovir
- Tebivudine
What is the best choice treatment of chronic Hep C?
PEG-INF + RBV
What are the 2 top causes of cirrhosis in the USA?
- Hep C
- Alcoholic Liver disease
- Hep C + alcoholic liver disease
What type of vaccine is the HBV vaccine and what is the schedule?
- HBsAg
- 0-1-6 month schedule
- Protective immunity: anti-HBsAb greater than 10IU/L
What is the preventive therapy for perinatal HBV transmission?
- HbIg (0.06mL/kg)
- HBV vaccine within 12 hours of birth (then 1-6-12m later)
- Efficacy = 95%
What are the 2 causes of reactive lymphadenopathy?
- Infectious disease
- Noninfective disease
- Infiltrative disease
What types of infectious orgs can cause lymphadenopathy?
- Viral: mono, rubella
- Bac: cat-scratch
- Mycobac: TB
- Spirochetal: syphilis, leptospirosis
- Chlamydial: lymphogranuloma venerum
- Fungal: Coccidioidomycosis
- Parasitic: Toxo
What noninfectious diseases cause lymphadenopathy?
- Sarcoidosis
- Connective tissue diseases: SLE
- Kawasaki's disease
- Drug hypersensitivity: phenytoin
- Silicone breast implantation
What types of diseases result in infiltrative lymphadenopahty?
Malignant: mets, melanoma, germ cell tumor, leukemia

- Lipid storage diseases: Gaucher's
- Amyloidosis
What are the 2 causes of primary lymphoproliferative lymphadenopahty?
- Lymphoma: Hodgkin's, non-Hodgkin's
- Malignant histiocytosis
What causes lymphadenopathy in 60% of cases of adults over 50 years of age?
malignancy
What are the causes of inguinal lymphadenopathy?
- Chacroid
- Lymphogranulma venerum
- Syphilis
- Genital herpes
- Granuloma ingiunale
What are the major causes of mediastinal & hilar lymphadenopathy?
- TB
- Endemic mycoses: Histo, Coccidio, Paracoccidio
What are the 2 main causes of acute suppurative lymphadenitis?
1) Staph aureus
2) Group A strep

Nodes involved: submandibular, cervical, ingiunal, axillary
What causes Cat-scratch disease?
Bartonella henselae
What is Parinaud's sign?
conjunctivitis with ipsilateral preauricular lymphadenitis

- seen in Cat-Scratch disease
What is the most common form of extrapulmonary TB?
- mycobacterial lymphadenitis
- if cervical = called scrofula
- location: unilateral on upper border of sternocleidomastoid muscle or supraclavicular, sometimes in the axilla
Is mycobacterial lymphadenitis painful?
no: uliateral, firm, red & painLESS
What are the top 3 causes of mycobacterial lyphadenitis?
1) M. bovis
2) M. tuberculosis
3) M. avium complex (MAC)
What are the symptoms of miliary TB?
- Systemic
- Generalized lymphadenopathy outside of the cervical chain
What are the 2 diseases that can cause inguinal lymphadenopathy?
- STDs: chancroid (H. ducreyi), C. trachomatis, syphilis, herpes, donovanosis
- Metastaic genital neoplasms
What often co-infects with H. ducreyi (Chancroid)?
- HSV or C. trachomatis
What is the inguinal lymphadenopathy of chancroid like?
- enlarged, painful, tender,(mostly unilateral) nodes
What is the inguinal lymphadenopathy of lymphogranuloma venerum like?
C. trachomatis
- vesicular lesion 1st
- 1-6 weeks later: unilateral, painful nodes
- IF untreaded: nodes rupture & a nonhealing fistula forms
What is the Groove sign?
- Cleavage of the enlarged nodes by the inguinal ligament
- Seen in lymphogranuloma venerum (C. trachomatis)
What are the symptoms of 2ndary syphilis?
- Generalized lymphadenopathy
- Skin lesions

- Appear 2-8 weeks after chancre heals
When does the chancre of syphilis appear?
14-30 days post inoculation
What are the lesions of genital herpes?
- vesicles: macules & papules followed by vesicles & ulcers
- Inguinal lymphadenopathy (uni or bilateral)
What sites in women are affected by genital herpes?
- Vulva + cervix
- Perineum
- Vagina
- Buttocks
- Perineal region
What sites in men are affected by genital herpes?
- Buttocks
- Anal & perianal area
What causes granuloma inguinale?
Calymmatobacterium granulomatis
What are the symptoms of grauloma inguinale (donovanosis)
- Papules on the penis within days of inoculation
- Rapidly ulcerate to form red, granulomatous painless ulcers that bleed easily on contact
What is oculogradular syndrome?
Tularemia symptom:
- conjunctivits
- conjunctival ulceration & papules on the eyelids
- inflammation of the Head & Neck lymph nodes.
What type of lymphadenopathy is almost universal in kids with primary TB?
Ipsilateral
What areas have endemic histoplasmosis?
- Mississippi river valley
- OhiO river valley
What areas have endemic coccidioidomycosis?
- Southwest US, Mexico & Central & South America

- Mediastinal & hilar lymph nodes
What areas have endemic paracoccidioidomycosis?
- Mexico, Central & South America

- Cervical, axillary & mediastinal with/out fistual formation
What often accompanies the bilateral symmetric hilar lymphadenopathy of sarcoidosis?
Paratracheal adenopathy
If a patient with aids presents with generalized lymphadenopathy, what should you think about?
- Lymphoma
- Kaposi's sarcoma
What drugs can cause lymphadenopathy?
- Phenytoin
- Carbamazepine
What vaccines can cause lymphadenopathy?
- Measles
- BCG
What autoimmune diseases can cause lymphadenopahty:
- Rheumatoid arthritis
- Juvenile rheumatoid arthritis
- active SLE
What is mucocutaneous lymph node syndrome?
lymphadenopathy due to Kawasaki's disease
What is ulcerograndular syndrome?
Tularemia infection: ulcer or pustule develops after up to 10 days post-exposure
What are the 4 main causes of generalized lymphaedenopathy?
1) Infective mono
2) HIV
3) Human T-lymphocyte leukemia virus 1
4) Tropical diseases
What tropical diseases cause lymphadenopathy?
- Leishmaniasis
- Filariasis
- Onchocerciasis
- Wuchereria bancrofti
- African trypanosomiasis
- (Chagas') tyrpanosomiasis
What are the sites (2+) where lymph node enlargement equals generalized lymphadenopathy?
- Posterior cervical
- Occipital
- Submandibular
- Axillary
What are the signs/symptoms of HTLV-1?
- Lymphadenopathy (most common)
- Skin lesions
- Hepatosplenomegaly
- Hypercalcemia
- Lymphocytosis
- Hyperimmunoglobulinemia
EKG "Sawtooth" P waves
- Classic ECG finding in atrial flutter.
Define unstable angina.
- Angina is new, is worsening, or occurs at rest
ACEI =
- Antihypertensive for a diabetic patient with proteinuria.
Beck's triad for cardiac tamponade.
- Hypotension, distant heart sounds, and JVD
3 Drug types that slow AV node transmission.
- β-blockers
- Digoxin
- Calcium channel blockers
What hypercholesterolemia treatment that → flushing and pruritus?
Niacin
What is the treatment for atrial fibrillation?
Anticoagulation, rate control, & cardioversion
What is the treatment for ventricular fibrillation?
Immediate cardioversion
What is the autoimmune complication occurring 2-4 weeks post-MI?
Dressler's syndrome: fever, pericarditis, ↑ ESR
IV drug use with JVD and holosystolic murmur at the left sternal border. Treatment?
Treat existing heart failure and replace the tricuspid valve
What is the diagnostic test for hypertrophic cardiomyopathy?
Echocardiogram (showing thickened left ventricular wall and outflow obstruction).
A fall in systolic BP of > 10 mmHg with inspiration is called ____.
Pulsus paradoxus (seen in cardiac tamponade)
Low-voltage, diffuse ST-segment elevation are _____
- Classic ECG findings in pericarditis.
What is the definition of hypertension?
BP > 140/90 on three separate occasions two weeks apart
What are the eight surgically correctable causes of hypertension?
- Renal artery stenosis
- Coarctation of the aorta
- Pheochromocytoma
- Conn's syndrome
- Cushing's syndrome
- Unilateral renal parenchymal disease
- Hyperthyroidism
- Hyperparathyroidism
What tests are used to evaluate a pulsatile abdominal mass and bruit?
Abdominal ultrasound and CT
What are the indications for surgical repair of abdominal aortic aneurysm?
> 5.5 cm, rapidly enlarging, symptomatic, or rupture
What is the treatment for acute coronary syndrome?
Morphine, O2, sublingual nitroglycerin, ASA, IV β-blockers, heparin
What is metabolic syndrome?
- Abdominal obesity
- High triglycerides
- Low HDL
- Hypertension
- Insulin resistance
- Prothrombotic or proinflammatory states
Exercise stress treadmill with ECG
What is the appropriate diagnostic test?
- A 50-year-old male with angina can exercise to 85% of maximum predicted heart rate.
Exercise stress treadmill with ECG
What is the appropriate diagnostic test?
- A 65-year-old woman with left bundle branch block and severe osteoarthritis has unstable angina.
Pharmacologic stress test (e.g., dobutamine echo)
What are the signs of active ischemia during stress testing?
Angina, ST-segment changes on ECG, or ↓ BP
What ECG findings suggest an MI?
ST-segment elevation (depression means ischemia), flattened T waves, and Q waves
ECG findings suggesting MI.
What's the dx?
- A young patient has angina at rest with ST-segment elevation. Cardiac enzymes are normal.
Prinzmetal's angina
What are the common symptoms associated with silent MIs?
CHF, shock, and altered mental status
What is the best diagnostic test for pulmonary embolism?
V/Q scan
What agent reverses the effects of heparin?
Protamine
What coagulation parameter is most affected by warfarin?
PT
What is the Dx?
- A young patient with a family history of sudden death collapses and dies while exercising.
Hypertrophic cardiomyopathy
Describe endocarditis prophylaxis regimens.
- Oral surgery—amoxicillin
- GI or GU procedures—ampicillin and gentamicin before and amoxicillin after
What are the 6 P's of ischemia due to peripheral vascular disease?
- Pain
- Pallor
- Pulselessness
- Paralysis
- Paresthesia
- Poikilothermia
What is Virchow's triad?
- Stasis
- Hypercoagulability
- Endothelial damage
What is the most common cause of hypertension in young women?
OCPs
What is the most common cause of hypertension in young men?
Excessive EtOH
What skin lesion has a "Stuck-on" appearance?
Seborrheic keratosis
What presents with red plaques with silvery-white scales and sharp margins?
- Psoriasis
What is the most common type of skin cancer?
Basal cell carcinoma: the lesion is a pearly-colored papule with a translucent surface and telangiectasias.
What's the Dx?
- Honey-crusted lesions.
- Impetigo
What is the Dx?
- A febrile patient with a history of diabetes presents with a red, swollen, painful lower extremity.
- Cellulitis
+ Nikolsky's sign =
- Pemphigus vulgaris
- Nikolsky's sign =
- Bullous pemphigoid
What's the Dx?
- A 55-year-old obese patient presents with dirty, velvety patches on the back of the neck.
- Acanthosis nigricans.
- NB: Check fasting blood sugar to rule out diabetes
Dermatomal distribution = ____
- Varicella zoster
Flat-topped papules =
Lichen planus
Iris-like target lesions = ___
Erythema multiforme
What's the Dx?
- A lesion characteristically occurring in a linear pattern in areas where skin comes into contact with clothing or jewelry.
- Contact dermatitis
What's the Dx?
- Presents with a herald patch, Christmas-tree pattern.
- Pityriasis rosea
What's the Dx?
- A 16-year-old presents with an annular patch of alopecia with broken-off, stubby hairs.
- Alopecia areata (autoimmune process)
What's the Dx?
- Pinkish, scaling, flat lesions on the chest and back. KOH prep has a "spaghetti-and-meatballs" appearance.
- Pityriasis versicolor
What's the Dx?
- Premalignant lesion from sun exposure that can → squamous cell carcinoma.
- Actinic keratosis
What's the lesion?
- "Dewdrop on a rose petal."
Lesions of 1° varicella
What's the Dx?
- "Cradle cap."
- Seborrheic dermatitis
- Treat with antifungals
What's the Dx?
- Associated with Propionibacterium acnes and changes in androgen levels.
- Acne vulgaris
What's the Dx?
- A painful, recurrent vesicular eruption of mucocutaneous surfaces.
- Herpes simplex
What's the Dx?
- Inflammation and epithelial thinning of the anogenital area, predominantly in in postmenopausal women.
- Lichen sclerosus
What's the Dx?
- Exophytic nodules on the skin with varying degrees of scaling or ulceration; the second most common type of skin cancer.
- Squamous cell carcinoma
What's the most common cause of hypothyroidism?
- Hashimoto's thyroiditis
What's the Dx?
- High TSH, low T4, antimicrosomal antibodies
- Hashimoto's thyroiditis.
What's the Dx?
- Exophthalmos, pretibial myxedema, and ↓ TSH.
- Graves' disease
What's the most common cause of Cushing's syndrome?
- Iatrogenic steroid administration.
- The second most common cause is Cushing's disease.
What's the Dx?
- A patient presents with signs of hypocalcemia, high phosphorus, and low PTH.
- Hypoparathyroidism
What's the Dx?
- "Stones, bones, groans, psychiatric overtones."
- Hypercalcemia
What's the Dx?
- A patient complains of headache, weakness, and polyuria; exam reveals hypertension and tetany. Labs reveals hypernatremia, hypokalemia, and metabolic alkalosis.
- 1° hyperaldosteronism (due to Conn's syndrome or bilateral adrenal hyperplasia)
What's the Dx?
- A patient presents with tachycardia, wild swings in BP, headache, diaphoresis, altered mental status, and a sense of panic.
- Pheochromocytoma
Should α- or β-antagonists be used first in treating pheochromocytoma?
- α-antagonists: phentolamine and phenoxybenzamine
What's the Dx?
- A patient with a history of lithium use presents with copious amounts of dilute urine.
- Nephrogenic diabetes insipidus (DI)
What's the treatment of central DI?
- Administration of DDAVP ↓ serum osmolality and free water restriction
What's the Dx?
- A postoperative patient with significant pain presents with hyponatremia and normal volume status.
- SIADH due to stress
Which antidiabetic agent is associated with lactic acidosis?
- Metformin
What's the Dx & Tx?
- A patient presents with weakness, nausea, vomiting, weight loss, and new skin pigmentation. Labs show hyponatremia and hyperkalemia.
- 1° adrenal insufficiency (Addison's disease).
- Treat with replacement glucocorticoids, mineralocorticoids, and IV fluids.
What's the goal hemoglobin A1c for a patient with DM?
< 7.0
What's the treatment of DKA?
- Fluids, insulin, and aggressive replacement of electrolytes (e.g., K+)
Why are β-blockers contraindicated in diabetics?
They can mask symptoms of hypoglycemia.
What bias is introduced into a study when a clinician is aware of the patient's treatment type?
Observational bias
Name the bias.
- Introduced when screening detects a disease earlier and thus lengthens the time from diagnosis to death.
- Lead-time bias
Name the bias.
- If you want to know if race affects infant mortality rate but most of the variation in infant mortality is predicted by socioeconomic status, then socioeconomic status is a _____.
- Confounding variable
The number of true positives divided by the number of patients with the disease is _____.
- Sensitivity
Sensitive tests have few false negatives and are used to rule _____ a disease.
- Out
PPD reactivity is used as a screening test because most people with TB (except those who are anergic) will have a +PPD. Highly sensitive or specific?
Highly sensitive for TB
Chronic diseases such as SLE—higher prevalence or incidence?
Higher prevalence
Epidemics such as influenza—higher prevalence or incidence?
- Higher incidence
Cross-sectional survey—incidence or prevalence?
- Prevalence
Cohort study—incidence or prevalence?
- Incidence and prevalence
Case-control study—incidence or prevalence?
Neither
Describe a test that consistently gives identical results, but the results are wrong.
High reliability, low validity.
What's the difference between a cohort and a case-control study.
Cohort studies can be used to calculate relative risk (RR), incidence, and/or odds ratio (OR). Case-control studies can be used to calculate an OR.
Attributable risk?
The incidence rate (IR) of a disease in exposed − the IR of a disease in unexposed.
Relative risk?
The IR of a disease in a population exposed to a particular factor ÷ the IR of those not exposed.
Odds ratio?
The likelihood of a disease among individuals exposed to a risk factor compared to those who have not been exposed
Number needed to treat?
1 ÷ (rate in untreated group − rate in treated group)
In which patients do you initiate colorectal cancer screening early?
- Patients with IBD
- Those with familial adenomatous polyposis (FAP)/hereditary nonpolyposis colorectal cancer (HNPCC)
- Those who have first-degree relatives with adenomatous polyps (< 60 years of age) or colorectal cancer
The most common cancer in men and the most common cause of death from cancer in men.
Prostate cancer is the most common cancer in men, but lung cancer causes more deaths.
The percentage of cases within one SD of the mean? Two SDs? Three SDs?
68%, 95.5%, 99.7%
Birth rate?
Number of live births per 1,000 population
Fertility rate?
Number of live births per 1000 women 15-44 years of age
Mortality rate?
Number of deaths per 1000 population
Neonatal mortality?
Number of deaths from birth to 28 days per 1000 live births
Postnatal mortality?
Number of deaths from 28 days to one year per 1,000 live births
Infant mortality?
Number of deaths from birth to one year of age per 1,000 live births (neonatal + postnatal mortality)
Fetal mortality?
Number of deaths from 20 weeks' gestation to birth per 1,000 total births
Perinatal mortality?
Number of deaths from 20 weeks' gestation to one month of life per 1,000 total births
Maternal mortality?
Number of deaths during pregnancy to 90 days postpartum per 100,000 live births
True or false: Once patients sign a statement giving consent, they must continue treatment.
False. Patients may change their minds at any time. Exceptions to the requirement of informed consent include emergency situations and patients without decision-making capacity.
A 15-year-old pregnant girl requires hospitalization for preeclampsia. Should her parents be informed?
No. Parental consent is not necessary for the medical treatment of pregnant minors.
What's the ethical issue?
- A doctor refers a patient for an MRI at a facility he/she owns.
- Conflict of interest
Involuntary psychiatric hospitalization can be undertaken for which three reasons?
The patient is a danger to self, a danger to others, or gravely disabled (unable to provide for basic needs)
True or false: Withdrawing life-sustaining care is ethically distinct from withholding sustaining care.
False. Withdrawing and withholding life are the same from an ethical standpoint.
When can a physician refuse to continue treating a patient on the grounds of futility?
When there is no rationale for treatment, maximal intervention is failing, a given intervention has already failed, and treatment will not achieve the goals of care.
What should you do?
- An eight-year-old child is in a serious accident. She requires emergent transfusion, but her parents are not present.
Treat immediately. Consent is implied in emergency situations.
Conditions in which confidentiality must be overridden.
Real threat of harm to third parties; suicidal intentions; certain contagious diseases; elder and child abuse
Involuntary commitment or isolation for medical treatment may be undertaken for what reason?
When treatment noncompliance represents a serious danger to public health (e.g., active TB).
A 10-year-old child presents in status epilepticus, but her parents refuse treatment on religious grounds.
Treat because the disease represents an immediate threat to the child's life. Then seek a court order.
What's to do?
- A son asks that his mother not be told about her recently discovered cancer.
A patient's family cannot require that a doctor withhold information from the patient
Patient presents with sudden onset of severe, diffuse abdominal pain. Exam reveals peritoneal signs and AXR reveals free air under the diaphragm. Management?
Emergent laparotomy to repair perforated viscus, likely stomach
The most likely cause of acute lower GI bleed in patients > 40 years old is _____.
- Diverticulosis
Diagnostic modality used when ultrasound is equivocal for cholecystitis.
HIDA scan
Sentinel loop on AXR.
Acute pancreatitis
What are risk factors for cholelithiasis?
Fat, female, fertile, forty, flatulent
Inspiratory arrest during palpation of the RUQ means ____.
Murphy's sign, seen in acute cholecystitis
Identify key organisms causing diarrhea:
- Most common organism
- Campylobacter
Identify key organisms causing diarrhea:
- Recent antibiotic use
- Clostridium difficile
Identify key organisms causing diarrhea:
- Camping
Giardia
Identify key organisms causing diarrhea:
- Traveler's diarrhea
ETEC
Identify key organisms causing diarrhea:
- Church picnics/mayonnaise
- S. aureus
Identify key organisms causing diarrhea:
- Uncooked hamburgers
E. coli O157:H7
Identify key organisms causing diarrhea:
- Fried rice
- Bacillus cereus
Identify key organisms causing diarrhea:
- Poultry/eggs
- Salmonella
Identify key organisms causing diarrhea:
- Raw seafood
Vibrio, HAV
Identify key organisms causing diarrhea:
- Patient has AIDS
- Isospora
- Cryptosporidium
- Mycobacterium avium complex (MAC)
Identify key organisms causing diarrhea:
- Pseudoappendicitis
- Yersinia
A 25-year-old Jewish male presents with pain and watery diarrhea after meals. Exam shows fistulas between the bowel and skin and nodular lesions on his tibias.
- Crohn's disease
Inflammatory disease of the colon with ↑ risk of colon cancer.
Ulcerative colitis
Extraintestinal manifestations of IBD =
- Uveitis
- Ankylosing spondylitis
- Pyoderma gangrenosum
- Erythema nodosum
- 1° sclerosing cholangitis
Medical treatment for IBD.
5-aminosalicylic acid +/− sulfasalazine and steroids during acute exacerbations
The difference between Mallory-Weiss and Boerhaave tears is
- Mallory-Weiss: superficial tear in the esophageal mucosa

- Boerhaave: full-thickness esophageal rupture
Charcot's triad =
RUQ pain, jaundice, and fever/chills in the setting of ascending cholangitis
Reynolds' pentad:
Charcot's triad plus shock & mental status changes, with suppurative ascending cholangitis
Medical treatment for hepatic encephalopathy.
- ↓ protein intake
- lactulose
- neomycin
What is the 1st step in the management of a patient with acute GI bleed?
Establish the ABCs
Most likely diagnosis and cause?
- A four-year-old child presents with oliguria, petechiae, and jaundice following an illness with bloody diarrhea.
Hemolytic-uremic syndrome (HUS) due to E. coli O157:H7
Post-HBV exposure treatment.
HBV immunoglobulin
Classic causes of drug-induced hepatitis.
- TB medications (INH, rifampin, pyrazinamide)
- Acetaminophen
- Tetracycline
What's the Dx?
- A 40-year-old obese female with elevated alkaline phosphatase, elevated bilirubin, pruritus, dark urine, and clay-colored stools.
Biliary tract obstruction
Hernia with highest risk of incarceration—indirect, direct, or femoral?
- Femoral hernia
A 50-year-old man with a history of alcohol abuse presents with boring epigastric pain that radiates to the back and is relieved by sitting forward. Management?
Confirm the diagnosis of acute pancreatitis with elevated amylase and lipase. Make patient NPO and give IV fluids, O2, analgesia, and "tincture of time"
Four causes of microcytic anemia.
TICS:
- Thalassemia
- Iron deficiency
- anemia of Chronic disease
- Sideroblastic anemia
An elderly male with hypochromic, microcytic anemia is asymptomatic. Diagnostic tests?
Fecal occult blood test and sigmoidoscopy; suspect colorectal cancer
Precipitants of hemolytic crisis in patients with G6PD deficiency:
- Sulfonamides
- Antimalarial drugs
- Fava beans
The most common inherited cause of hypercoagulability.
Factor V Leiden mutation
The most common inherited hemolytic anemia.
Hereditary spherocytosis
The diagnostic test for hereditary spherocytosis is ___.
Osmotic fragility test
Diamond-Blackfan anemia is ___
- Pure RBC aplasia.
Which anemia is associated with absent radii and thumbs, diffuse hyperpigmentation, café-au-lait spots, microcephaly, and pancytopenia?
- Fanconi's anemia
Medications and viruses that → aplastic anemia.
MEDS: Chloramphenicol, sulfonamides, radiation, chemotherapeutic agents

VIRUSES: HIV, hepatitis, parvovirus B19, EBV
How to distinguish polycythemia vera from 2° polycythemia.
Both have ↑ hematocrit and RBC mass, but polycythemia vera should have normal O2 saturation and low erythropoietin levels
Thrombotic thrombocytopenic purpura (TTP) pentad?
Pentad of TTP—"FAT RN":

- Fever
- Anemia
- Thrombocytopenia

- Renal dysfunction
- Neurologic abnormalities
HUS triad?
Anemia, thrombocytopenia, and acute renal failure
Treatment for TTP.
Emergent large-volume plasmapheresis, corticosteroids, antiplatelet drugs
What is the treatment for idiopathic thrombocytopenic purpura (ITP) in children?
Usually resolves spontaneously; may require IVIG and/or corticosteroids
Which of the following are ↑ in DIC: fibrin split products, D-dimer, fibrinogen, platelets, and hematocrit.
Fibrin split products and D-dimer are elevated; platelets, fibrinogen, and hematocrit are ↓.
An eight-year-old boy presents with hemarthrosis and ↑ PTT with normal PT and bleeding time. Diagnosis? Treatment?
Hemophilia A or B; consider desmopressin (for hemophilia A) or factor VIII or IX supplements.
A 14-year-old girl presents with prolonged bleeding after dental surgery and with menses, normal PT, normal or ↑ PTT, and ↑ bleeding time. Diagnosis? Treatment?
- von Willebrand's disease
- Treat with desmopressin, FFP, or cryoprecipitate
A 60-year-old African-American male presents with bone pain. His workup for multiple myeloma might reveal?
Monoclonal gammopathy, Bence Jones proteinuria, "punched-out" lesions on x-ray of the skull and long bones
Hodgkin's lymphoma histo =
Reed-Sternberg cells
A 10-year-old boy presents with fever, weight loss, and night sweats. Examination shows anterior mediastinal mass. Suspected diagnosis?
Non-Hodgkin's lymphoma
Microcytic anemia with ↓ serum iron, ↓ total iron-binding capacity (TIBC), and normal or ↑ ferritin.
- Anemia of chronic disease
Microcytic anemia with ↓ serum iron, ↓ ferritin, and ↑ TIBC.
Iron deficiency anemia
An 80-year-old man presents with fatigue, lymphadenopathy, splenomegaly, and isolated lymphocytosis. Suspected diagnosis?
Chronic lymphocytic leukemia (CLL)
A late, life-threatening complication of chronic myelogenous leukemia (CML).
Blast crisis (fever, bone pain, splenomegaly, pancytopenia)
Auer rods on blood smear.
Acute myelogenous leukemia (AML)
AML subtype associated with DIC.
M3
Electrolyte changes in tumor lysis syndrome:
↓ Ca2+
↑ K−
↑ phosphate
↑ uric acid
What's the treatment for AML M3?
Retinoic acid
A 50-year-old male presents with early satiety, splenomegaly, and bleeding. Cytogenetics show t(9,22). Diagnosis?
CML
Intracellular inclusions seen in thalassemia, G6PD deficiency, and postsplenectomy?
- Heinz bodies
An autosomal-recessive disorder with a defect in the GPIIbIIIa platelet receptor and ↓ platelet aggregation.
Glanzmann's thrombasthenia
Virus associated with aplastic anemia in patients with sickle cell anemia.
Parvovirus B19
A 25-year-old African-American male with sickle cell anemia has sudden onset of bone pain. Management of pain crisis?
- O2
- Analgesia
- Hydration

- and, if severe, transfusion
A significant cause of morbidity in thalassemia patients. Treatment?
Iron overload; use deferoxamine
The three most common causes of fever of unknown origin (FUO).
Infection, cancer, and autoimmune disease
Four signs and symptoms of streptococcal pharyngitis.
Fever, pharyngeal erythema, tonsillar exudate, lack of cough
A nonsuppurative complication of streptococcal infection that is not altered by treatment of 1° infection.
Postinfectious glomerulonephritis
Asplenic patients are particularly susceptible to these organisms.
Encapsulated organisms:
- Pneumococcus
- Meningococcus
- Haemophilus influenzae
- Klebsiella
The number of bacterial culture on a clean-catch specimen to diagnose a UTI:
- 105 bacteria/mL
Which healthy population is susceptible to UTIs?
- Pregnant women
- Treat this group aggressively because of potential complications
A patient from California or Arizona presents with fever, malaise, cough, and night sweats. Diagnosis? Treatment?
- Coccidioidomycosis.
- Rx: Amphotericin B
Nonpainful chancre.
1° syphilis
A "blueberry muffin" rash is characteristic of what congenital infection?
- Rubella
Meningitis in neonates. Causes? Treatment?
- Dx: Group B strep, E. coli, Listeria.
- Tx: ampicillin & gentamicin
Meningitis in infants. Causes? Treatment?
Causes: Pneumococcus, meningococcus, H. influenzae.

Tx: cefotaxime & vancomycin
What should always be done prior to LP?
Check for ↑ ICP; look for papilledema
Bacterial meningitis CSF findings:
Low glucose
PMN predominance
Aseptic (viral) meningitis
CSF findings:
- Normal glucose
- Lymphocytic predominance
Subarachnoid hemorrhage (SAH)
CSF findings:
- Numerous RBCs in serial CSF samples
MS CSF findings:
- ↑ gamma globulins
Initially presents with a pruritic papule with regional lymphadenopathy and evolves into a black eschar after 7-10 days. Treatment?
- Cutaneous anthrax.
- Treat with penicillin G or ciprofloxacin
Findings in 3° syphilis.
Tabes dorsalis, general paresis, gummas, Argyll Robertson pupil, aortitis, aortic root aneurysms.
Characteristics of 2° Lyme disease.
- Arthralgias
- Migratory polyarthropathies
- Bell's palsy
- Myocarditis
Cold agglutinins =
Mycoplasma
A 24-year-old male presents with soft white plaques on his tongue and the back of his throat. Diagnosis? Workup? Treatment?
- Candidal thrush.
- Workup should include an HIV test.
- Treat with nystatin oral suspension
Begin Pneumocystis carinii pneumonia (PCP) prophylaxis in an HIV-positive patient at what CD4 count? Mycobacterium avium-intracellulare (MAI) prophylaxis?
≤ 200 for PCP (with TMP); ≤ 50-100 for MAI (with clarithromycin/azithromycin)
Risk factors for pyelonephritis.
- Pregnancy
- Vesicoureteral reflux
- Anatomic anomalies
- Indwelling catheters
- Kidney stones
Neutropenic nadir postchemotherapy.
7-10 days
Lesion of 1° Lyme disease:
- Erythema migrans.
Classic physical findings for endocarditis.
- Fever
- Heart murmur
- Osler's nodes,
- Splinter hemorrhages
- Janeway lesions
- Roth's spots
- Aplastic crisis in sickle cell disease.
- Parvovirus B19
Ring-enhancing brain lesion on CT with seizures:
Taenia solium (cysticercosis)
Name the organism:
- Branching rods in oral infection.
Actinomyces israelii
Name the organism:
- Painful chancroid.
Haemophilus ducreyi
Name the organism:
- Dog or cat bite.
Pasteurella multocida
Name the organism:
- Gardener.
Sporothrix schenckii
Name the organism:
- Pregnant women with pets.
Toxoplasma gondii
Name the organism:
- Meningitis in adults.
Neisseria meningitidis
Name the organism:
- Meningitis in elderly.
Streptococcus pneumoniae
Name the organism:
- Alcoholic with pneumonia
Klebsiella
Name the organism:
- "Currant jelly" sputum.
Klebsiella
Name the organism:
- Infection in burn victims
Pseudomonas
Name the organism:
- Osteomyelitis from foot wound puncture.
Pseudomonas
Name the organism:
- Osteomyelitis in a sickle cell patient.
Salmonella
A 55-year-old man who is a smoker and a heavy drinker presents with a new cough and flulike symptoms. Gram stain shows no organisms; silver stain of sputum shows gram-negative rods. What is the diagnosis?
Legionella pneumonia
A middle-aged man presents with acute-onset monoarticular joint pain and bilateral Bell's palsy. What is the likely diagnosis, and how did he get it? Treatment?
- Dx: Lyme disease
- Cause: Ixodes tick
- Rx: Doxycycline
A patient develops endocarditis three weeks after receiving a prosthetic heart valve. What organism is suspected?
S. aureus or S. epidermidis
A patient presents with pain on passive movement, pallor, poikilothermia, paresthesias, paralysis, and pulselessness. Treatment?
All-compartment fasciotomy for suspected compartment syndrome
Back pain that is exacerbated by standing and walking and relieved with sitting and hyperflexion of the hips.
Spinal stenosis
Joints in the hand affected in rheumatoid arthritis.
MCP and PIP joints
DIP joints are spared
Joint pain and stiffness that worsen over the course of the day and are relieved by rest.
Osteoarthritis
Genetic disorder associated with multiple fractures and commonly mistaken for child abuse.
Osteogenesis imperfecta
Hip and back pain along with stiffness that improves with activity over the course of the day and worsens at rest. Diagnostic test?
Suspect ankylosing spondylitis. Check HLA-B27
Arthritis, conjunctivitis, and urethritis in young men. Associated organisms?
- Campylobacter
- Shigella
- Salmonella
- Chlamydia
- Ureaplasma
A 55-year-old man has sudden, excruciating first MTP joint pain after a night of drinking red wine. Diagnosis, workup, and chronic treatment?
Gout. Needle-shaped, negatively birefringent crystals are seen on joint fluid aspirate. Chronic treatment with allopurinol or probenecid
Rhomboid-shaped, positively birefringent crystals on joint fluid aspirate.
Pseudogout
An elderly female presents with pain and stiffness of the shoulders and hips; she cannot lift her arms above her head. Labs show anemia and ↑ ESR.
Polymyalgia rheumatica
An active 13-year-old boy has anterior knee pain. Diagnosis?
Osgood-Schlatter disease
Bone is fractured in fall on outstretched hand.
Distal radius (Colles' fracture)
Complication of scaphoid fracture.
Avascular necrosis
Signs suggesting radial nerve damage with humeral fracture.
Wrist drop, loss of thumb abduction
A young child presents with proximal muscle weakness, waddling gait, and pronounced calf muscles.
Duchenne muscular dystrophy
A first-born female who was born in breech position is found to have asymmetric skin folds on her newborn exam. Diagnosis? Treatment?
Developmental dysplasia of the hip. If severe, consider a Pavlik harness to maintain abduction
An 11-year-old obese, African-American boy presents with sudden onset of limp. Diagnosis? Workup?
Slipped capital femoral epiphyses. AP and frog-leg lateral view
The most common 1° malignant tumor of bone.
Multiple myeloma
Unilateral, severe periorbital headache with tearing and conjunctival erythema.
Cluster headache
Prophylactic treatment for migraine.
β-blockers, Ca2+ channel blockers, TCAs
The most common pituitary tumor. Treatment?
Prolactinoma. Dopamine agonists (e.g., bromocriptine)
A 55-year-old patient presents with acute "broken speech." What type of aphasia? What lobe and vascular distribution?
- Broca's aphasia
- Frontal lobe, left MCA distribution
The second most common is berry aneurysm.
The most common cause of SAH.
Trauma
A crescent-shaped hyperdensity on CT that does not cross the midline.
Subdural hematoma—bridging veins torn
A history significant for initial altered mental status with an intervening lucid interval. Diagnosis? Most likely etiology? Treatment?
Epidural hematoma. Middle meningeal artery. Neurosurgical evacuation
CSF findings with SAH.
Elevated ICP, RBCs, xanthochromia
Albuminocytologic dissociation.
Guillain-Barré (↑ protein in CSF with only a modest ↑ in cell count)
Cold water is flushed into a patient's ear, and the fast phase of the nystagmus is toward the opposite side. Normal or pathological?
Normal
The most common 1° sources of metastases to the brain.
Lung, breast, skin (melanoma), kidney, GI tract
May be seen in children who are accused of inattention in class and confused with ADHD.
Absence seizures
The most frequent presentation of intracranial neoplasm.
Headache
The most common cause of seizures in children (2-10 years).
Infection, febrile seizures, trauma, idiopathic
The most common cause of seizures in young adults (18-35 years).
Trauma, alcohol withdrawal, brain tumor
First-line medication for status epilepticus.
IV benzodiazepine
Confusion, confabulation, ophthalmoplegia, ataxia.
Wernicke's encephalopathy due to a deficiency of thiamine.
What % lesion is an indication for carotid endarterectomy?
Seventy percent IF the stenosis is symptomatic.
The most common causes of dementia.
Alzheimer's and multi-infarct
Combined UMN and LMN disorder.
ALS
Rigidity and stiffness with resting tremor and masked facies.
Parkinson's disease
The mainstay of Parkinson's therapy.
Levodopa/carbidopa
Treatment for Guillain-Barré syndrome.
IVIG or plasmapheresis
Rigidity and stiffness that progress to choreiform movements, accompanied by moodiness and altered behavior.
Huntington's disease
A six-year-old girl presents with a port-wine stain in the V2 distribution as well as with mental retardation, seizures, and leptomeningeal angioma.
- Sturge-Weber syndrome.
- Treat symptomatically. Possible focal cerebral resection of affected lobe
Café-au-lait spots on skin.
Neurofibromatosis 1
Hyperphagia, hypersexuality, hyperorality, and hyperdocility.
Klüver-Bucy syndrome (amygdala)
Administer to a symptomatic patient to diagnose myasthenia gravis.
Edrophonium
1° causes of third-trimester bleeding.
Placental abruption & placenta previa
Classic ultrasound and gross appearance of complete hydatidiform mole.
Snowstorm on ultrasound. "Cluster-of-grapes" appearance on gross examination.
Chromosomal pattern of a complete mole.
46,XX
Molar pregnancy containing fetal tissue.
Partial mole
Symptoms of placental abruption:
Continuous, painful vaginal bleeding
Self-limited, painless vaginal bleeding
Symptoms of placenta previa.
When should a vaginal exam be performed with suspected placenta previa?
Never
Antibiotics with teratogenic effects.
- Tetracycline
- Fluoroquinolones
- Aminoglycosides
- Sulfonamides
Shortest AP diameter of the pelvis.
Obstetric conjugate: between the sacral promontory and the midpoint of the symphysis pubis
Medication given to accelerate fetal lung maturity.
Betamethasone or dexamethasone × 48 hours
The most common cause of postpartum hemorrhage.
Uterine atony
Treatment for postpartum hemorrhage.
Uterine massage; if that fails, give oxytocin
Typical antibiotics for group B streptococcus (GBS) prophylaxis.
IV penicillin or ampicillin
A patient fails to lactate after an emergency C-section with marked blood loss.
Sheehan's syndrome (postpartum pituitary necrosis)
Uterine bleeding at 18 weeks' gestation; no products expelled; membranes ruptured; cervical os open.
Inevitable abortion
Uterine bleeding at 18 weeks' gestation; no products expelled; cervical os closed.
Threatened abortion
The first test to perform when a woman presents with amenorrhea.
β-hCG; the most common cause of amenorrhea is pregnancy
Term for heavy bleeding during and between menstrual periods.
Menometrorrhagia
Cause of amenorrhea with normal prolactin, no response to estrogen-progesterone challenge, and a history of D&C.
Asherman's syndrome
Therapy for polycystic ovarian syndrome.
Weight loss and OCPs
Medication used to induce ovulation.
Clomiphene citrate
Diagnostic step required in a postmenopausal woman who presents with vaginal bleeding.
Endometrial biopsy
Indications for medical treatment of ectopic pregnancy.
Stable, unruptured ectopic pregnancy of 3.5 cm at 6 weeks' gestation
Medical options for endometriosis.
OCPs, danazol, GnRH agonists
"Chocolate cysts," powder burns
Laparoscopic findings in endometriosis.
The most common location for an ectopic pregnancy.
Ampulla of the oviduct
How to diagnose and follow a leiomyoma.
Ultrasound
Natural history of a leiomyoma.
Regresses after menopause
A patient has ↑ vaginal discharge & petechial patches in the upper vagina and cervix.
Trichomonas vaginitis
Treatment for bacterial vaginosis.
Oral or topical metronidazole
The most common cause of bloody nipple discharge.
Intraductal papilloma
Unopposed estrogen is contraindicated in which cancers?
Endometrial or estrogen receptor-  breast cancer
A patient presents with recent PID with RUQ pain.
Consider Fitz-Hugh-Curtis syndrome
Breast malignancy presenting as itching, burning, and erosion of the nipple.
Paget's disease
Annual screening for women with a strong family history of ovarian cancer.
CA-125 and transvaginal ultrasound
A 50-year-old woman leaks urine when laughing or coughing. Nonsurgical options?
Kegel exercises, estrogen, pessaries for stress incontinence
A 30-year-old woman has unpredictable urine loss. Examination is normal. Medical options?
Anticholinergics (oxybutynin) or β-adrenergics (metaproterenol) for urge incontinence.
Lab values suggestive of menopause.
↑ serum FSH
The most common cause of female infertility.
Endometriosis
Two consecutive findings of atypical squamous cells of undetermined significance (ASCUS) on Pap smear. Follow-up evaluation?
Colposcopy and endocervical curettage
Breast cancer type that ↑ the future risk of invasive carcinoma in both breasts.
Lobular carcinoma in situ
Nontender abdominal mass associated with elevated VMA and HVA.
Neuroblastoma
The most common type of tracheoesophageal fistula (TEF). Diagnosis?
Esophageal atresia with distal TEF (85%). Unable to pass NG tube
Not contraindications to vaccination.
Mild illness &/or low-grade fever, current antibiotic therapy, and prematurity
Tests to rule out shaken baby syndrome.
Ophthalmologic exam, CT, and MRI
Diagnosis?
- A neonate has meconium ileus.
CF or Hirschsprung's disease
Bilious emesis within hours after the first feeding.
Duodenal atresia
A two-month-old presents with nonbilious projectile emesis. What are the appropriate steps in management?
- Correct metabolic abnormalities. - Then correct pyloric stenosis with pyloromyotomy
The most common 1° immunodeficiency.
Selective IgA deficiency
An infant has a high fever and onset of rash as fever breaks. What is he at risk for?
Febrile seizures (roseola infantum)
Acute-phase treatment for Kawasaki disease.
High-dose aspirin for inflammation and fever; IVIG to prevent coronary artery aneurysms
Treatment for mild and severe unconjugated hyperbilirubinemia.
Phototherapy (mild) or exchange transfusion (severe)
Sudden onset of mental status changes, emesis, and liver dysfunction after taking aspirin.
Reye's syndrome
A child has loss of red light reflex. Diagnosis?
Suspect retinoblastoma
Vaccinations at a six-month well-child visit.
HBV, DTaP, Hib, IPV, PCV
Precocious puberty
Tanner stage 3 in a six-year-old female.
Infection of small airways with epidemics in winter and spring.
RSV bronchiolitis
Cause of neonatal RDS.
Surfactant deficiency
What is the immunodeficiency?
- A boy has chronic respiratory infections.
Chronic granulomatous disease
- Nitroblue tetrazolium test is +.
What is the immunodeficiency?
- A child has eczema, thrombocytopenia, & high levels of IgA.
Wiskott-Aldrich Syndrome
What is the immunodeficiency?
- A four-month-old boy has life-threatening Pseudomonas infection.
Bruton's X-linked agammaglobulinemia
A condition associated with red "currant-jelly" stools.
Intussusception
A congenital heart disease that cause 2° hypertension.
Coarctation of the aorta
First-line treatment for otitis media.
Amoxicillin × 10 days
The most common pathogen causing croup.
Parainfluenza virus type 1
A homeless child is small for his age and has peeling skin and a swollen belly.
Kwashiorkor (protein malnutrition)
Gout, self-mutilation, and choreoathetosis
Lesch-Nyhan syndrome
- purine salvage problem with
defect in an X-linked syndrome with mental retardation, HGPRTase deficiency
A newborn female has continuous "machinery murmur."
Patent ductus arteriosus (PDA)
First-line pharmacotherapy for depression.
SSRIs
Antidepressants associated with hypertensive crisis.
MAOIs
Galactorrhea, impotence, menstrual dysfunction, and ↓ libido.
Patient on dopamine antagonist
A 17-year-old female has left arm paralysis after her boyfriend dies in a car crash. No medical cause is found.
Conversion disorder
Name the defense mechanism:
- A mother who is angry at her husband yells at her child.
Displacement
Name the defense mechanism:
- A pedophile enters a monastery.
Reaction formation
Name the defense mechanism:
- A woman calmly describes a grisly murder.
Isolation
Name the defense mechanism:
- A hospitalized 10-year-old begins to wet his bed.
Regression
Life-threatening muscle rigidity, fever, and rhabdomyolysis.
Neuroleptic malignant syndrome
Amenorrhea, bradycardia, and abnormal body image in a young female.
Anorexia
A 35-year-old male has recurrent episodes of palpitations, diaphoresis, and fear of going crazy.
Panic disorder
The most serious side effect of clozapine.
Agranulocytosis
A 21-year-old male has three months of social withdrawal, worsening grades, flattened affect, and concrete thinking.
Schizophreniform disorder (diagnosis of schizophrenia requires ≥ 6 months of symptoms)
Key side effects of atypical antipsychotics.
Weight gain, type 2 DM, QT prolongation
A young weight lifter receives IV haloperidol and complains that his eyes are deviated sideways. Diagnosis? Treatment?
- Acute dystonia (oculogyric crisis).
- Treat with benztropine or diphenhydramine
Medication to avoid in patients with a history of alcohol withdrawal seizures.
Neuroleptics
A 13-year-old male has a history of theft, vandalism, and violence toward family pets.
Conduct disorder
A five-month-old girl has ↓ head growth, truncal dyscoordination, and ↓ social interaction.
Rett's disorder
A patient hasn't slept for days, lost $20,000 gambling, is agitated, and has pressured speech. Diagnosis? Treatment?
Acute mania. Start a mood stabilizer (e.g., lithium)
After a minor fender bender, a man wears a neck brace and requests permanent disability.
Malingering.
A nurse presents with severe hypoglycemia; blood analysis reveals no elevation in C peptide.
Factitious disorder (Munchausen syndrome)
A patient continues to use cocaine after being in jail, losing his job, and not paying child support.
Substance abuse
A violent patient has vertical and horizontal nystagmus.
Phencyclidine hydrochloride (PCP) intoxication
A woman who was abused as a child frequently feels outside of or detached from her body.
Depersonalization disorder
Frotteurism (a paraphilia)
A man has repeated, intense urges to rub his body against unsuspecting passengers on a bus.
A schizophrenic patient takes haloperidol for one year and develops uncontrollable tongue movements. Diagnosis? Treatment?
- Tardive dyskinesia
- ↓ or discontinue haloperidol and consider another antipsychotic (e.g., risperidone, clozapine)
A man unexpectedly flies across the country, takes a new name, and has no memory of his prior life.
Dissociative fugue
Risk factors for DVT.
Stasis, endothelial injury and hypercoagulability (Virchow's triad)
Criteria for exudative effusion:
- Pleural/serum protein > 0.5
- Pleural/serum LDH > 0.6
Causes of exudative effusion.
Think of leaky capillaries:
- Malignancy
- TB
- Bacterial or viral infection
- Pulmonary embolism with infarct
- Pancreatitis
Causes of transudative effusion.
Think of intact capillaries:
- CHF
- Liver or kidney disease
- Protein-losing enteropathy
Normalizing PCO2 in a patient having an asthma exacerbation may indicate?
Fatigue & impending respiratory failure
Dyspnea, lateral hilar lymphodenopathy on CXR, noncaseating granulomas, increased ACE, and hypercalcemia.
Sarcoidosis
PFT showing ↓ FEV1/FVC.
Obstructive pulmonary disease (e.g., asthma)
PFT showing ↑ FEV1/FVC.
Restrictive pulmonary disease
Honeycomb pattern on CXR. Diagnosis? Treatment?
- Diffuse interstitial pulmonary fibrosis.
- Supportive care.
- Steroids may help.
Treatment for SVC syndrome.
Radiation
Treatment for mild, persistent asthma.
Inhaled β-agonists and inhaled corticosteroids
Acid-base disorder in pulmonary embolism.
Hypoxia & hypocarbia
Non-small cell lung cancer (NSCLC) associated with hypercalcemia.
Squamous cell carcinoma
Lung cancer associated with SIADH.
Small cell lung cancer (SCLC)
Lung cancer highly related to cigarette exposure.
SCLC
A tall white male presents with acute shortness of breath. Diagnosis? Treatment?
- Spontaneous pneumothorax.
- Spontaneous regression.
- Supplemental O2 may be helpful
Treatment of tension pneumothorax.
Immediate needle thoracostomy
Characteristics favoring carcinoma in an isolated pulmonary nodule.
- Age 45-50 years
- Lesions new or larger in comparison to old films
- Absence of calcification or irregular calcification
- 2 cm; irregular margins
Hypoxemia and pulmonary edema with normal pulmonary capillary wedge pressure.
ARDS
↑ risk of what infection with silicosis?
Mycobacterium tuberculosis
Causes of hypoxemia.
- Right-to-left shunt
- Hypoventilation
- Low inspired O2 tension
- Diffusion defect
- V/Q mismatch
Classic CXR findings for pulmonary edema.
- Cardiomegaly
- Prominent pulmonary vessels
- Kerley B lines
- "bat's-wing" appearance of hilar shadows
- Perivascular and peribronchial cuffing
Renal tubular acidosis (RTA) associated with abnormal H+ secretion and nephrolithiasis.
Type I (distal) RTA
RTA associated with abnormal HCO3 − and rickets.
Type II (proximal) RTA
RTA associated with aldosterone defect.
Type IV (distal) RTA
"Doughy skin."
Hypernatremia
Differential of hypervolemic hyponatremia.
Cirrhosis, CHF, nephritic syndrome
Chvostek's and Trousseau's signs.
Hypocalcemia
The most common causes of hypercalcemia.
Malignancy and hyperparathyroidism
T-wave flattening and U waves.
Hypokalemia
Peaked T waves and widened QRS.
Hyperkalemia
First-line treatment for moderate hypercalcemia.
IV hydration and loop diuretics (furosemide)
Type of ARF in a patient with FeNa < 1%.
Prerenal
A 49-year-old male presents with acute-onset flank pain and hematuria.
Nephrolithiasis
The most common type of nephrolithiasis.
Calcium oxalate
A 20-year-old man presents with a palpable flank mass and hematuria. Ultrasound shows bilateral enlarged kidneys with cysts. Associated brain anomaly?
Cerebral berry aneurysms (AD PCKD)
Hematuria, hypertension, and oliguria.
Nephritic syndrome
Proteinuria, hypoalbuminemia, hyperlipidemia, hyperlipiduria, edema.
Nephrotic syndrome
The most common form of nephritic syndrome.
Membranous glomerulonephritis
The most common form of glomerulonephritis.
IgA nephropathy (Berger's disease)
Glomerulonephritis with deafness.
Alport's syndrome
Glomerulonephritis with hemoptysis.
Wegener's granulomatosis and Goodpasture's syndrome
Presence of red cell casts in urine sediment.
Glomerulonephritis/nephritic syndrome
Eosinophils in urine sediment.
Allergic interstitial nephritis
Waxy casts in urine sediment and Maltese crosses (seen with lipiduria).
Nephrotic syndrome
Drowsiness, asterixis, nausea, and a pericardial friction rub.
Uremic syndrome seen in patients with renal failure.
A 55-year-old man is diagnosed with prostate cancer. Treatment options?
Wait, surgical resection, radiation &/or androgen suppression
Low urine specific gravity in the presence of high serum osmolality.
DI
Treatment of SIADH?
Fluid restriction, demeclocycline
Hematuria, flank pain, and palpable flank mass.
Renal cell carcinoma (RCC)
Testicular cancer associated with β-hCG, AFP.
Choriocarcinoma
The most common type of testicular cancer.
Seminoma: a type of germ cell tumor
The most common histology of bladder cancer.
Transitional cell carcinoma
Complication of overly rapid correction of hyponatremia.
Central pontine myelinolysis
Salicylate ingestion → in what type of acid-base disorder?
Anion gap acidosis and 1° respiratory alkalosis due to central respiratory stimulation
Acid-base disturbance commonly seen in pregnant women.
Respiratory alkalosis
Three systemic diseases → nephrotic syndrome.
DM, SLE, & amyloidosis
Elevated erythropoietin level, elevated hematocrit, and normal O2 saturation suggest?
RCC or other erythropoietin-producing tumor; evaluate with CT scan
A 55-year-old man presents with irritative and obstructive urinary symptoms. Treatment options?
Likely BPH. Options include no treatment, terazosin, finasteride, or surgical intervention (TURP)
Class of drugs that may cause syndrome of muscle rigidity, hyperthermia, autonomic instability, and extrapyramidal symptoms.
Antipsychotics (neuroleptic malignant syndrome)
Side effects of corticosteroids.
- Acute mania
- Immunosuppression
- Thin skin
- Osteoporosis
- Easy bruising
- Myopathies
Treatment for DTs.
Benzodiazepines
Treatment for acetaminophen overdose.
N-acetylcysteine
Treatment for opioid overdose.
Naloxone
Treatment for benzodiazepine overdose.
Flumazenil
Treatment for neuroleptic malignant syndrome.
Dantrolene or bromocriptine
Treatment for malignant hypertension.
Nitroprusside
Treatment of AF.
Rate control, rhythm conversion, and anticoagulation
Treatment of supraventricular tachycardia (SVT).
Rate control with carotid massasge or other vagal stimulation
Causes of drug-induced SLE.
INH, penicillamine, hydralazine, procainamide
Macrocytic, megaloblastic anemia with neurologic symptoms.
B12 deficiency
Macrocytic, megaloblastic anemia without neurologic symptoms.
Folate deficiency
A burn patient presents with cherry-red flushed skin and coma. SaO2 is normal, but carboxyhemoglobin is elevated. Treatment?
Treat CO poisoning with 100% O2 or with hyperbaric O2 if severe poisoning or pregnant
Blood in the urethral meatus or high-riding prostate.
Bladder rupture or urethral injury
Test to rule out urethral injury.
Retrograde cystourethrogram
Radiographic evidence of aortic disruption or dissection.
Widened mediastinum (> 8 cm), loss of aortic knob, pleural cap, tracheal deviation to the right, depression of left main stem bronchus
Radiographic indications for surgery in patients with acute abdomen.
Free air under the diaphragm, extravasation of contrast, severe bowl distention, space-occupying lesion (CT), mesenteric occlusion (angiography)
The most common organism in burn-related infections.
Pseudomonas
Method of calculating fluid repletion in burn patients.
Parkland formula
Acceptable urine output in a trauma patient.
50 cc/hour
Acceptable urine output in a stable patient.
30 cc/hour
Cannon "a" waves.
Third-degree heart block
Signs of neurogenic shock.
Hypotension & bradycardia
Cushing's triad:
Signs of ↑ ICP: Hypertension, bradycardia, and abnormal respirations
Hypovolemic shock
↓ CO, ↓ pulmonary capillary wedge pressure (PCWP), ↑ peripheral vascular resistance (PVR).
↓ CO, ↑ PCWP, ↑ PVR.
Cardiogenic shock
↑ CO, ↓ PCWP, ↓ PVR.
Septic or anaphylactic shock
Treatment of septic shock.
Fluids and antibiotics
Identify cause; pressors (e.g., dobutamine)
Treatment of cardiogenic shock.
Identify cause; fluid and blood repletion
Treatment of hypovolemic shock.
Treatment of anaphylactic shock.
Diphenhydramine or epinephrine 1:1000
Continuous positive airway pressure
Supportive treatment for ARDS.
A patient with chest trauma who was previously stable suddenly dies
Signs of air embolism.
AP chest, AP/lateral C-spine, AP pelvis
Trauma series.
Define Delusion of Reference.
Events, objects, or persons in one's environment that are belieed to have particular personal significance
Define Circumstantial thinking.
Communication of unnecessary details before finally arriving at the central idea
Define delusion.
A false belief not supported by fact and cannot be challenged successfully by logic or reasoning
Define Intermittent explosive disorder.
Discrete episodes of aggression and destruction out of proportion with the precipitant stressor. EEG changes in 55%
Define Illusion.
A misinterpretation of a real sensory stimulus. common in ppl w.out psych disorders also. content affected by person's state of mind, wishes, and fears
Normal pre and postnatal development but lose previously acquired purposeful hand skills between 5-30 mos. Stereotyped hand movements, poor coordination. A PDD
Rett's disorder
Define Orientation.
State of awareness of time, place, identity of oneself and others
Personality disorder
preoccupation with perfection, orderliness, and control. Lose main point of activity because they pay too much attention to details and rules
OCPD/ obsessive compulsive personality disorder
IQ 35-55%. function at preschool to second grade level
moderate mental retardation
Lose ability to form abstract concepts. nml in kids, also seen in MR, dementia, and schizophrenia
Concrete thinking
Voluntary assumption of an inappropriate or bizarre posture for long periods of time. usually seen in schizophrenia, esp catatonic type
Catatonic posturing
Psychotherapists transference response to the pt
Countertransference
Perception of a stimulus when none is present. auditory most common in psychosis; tactile, visual, gustatory, olfactory, or kinesthetic in neuro d/o's
Hallucination
Capacity to generalize and formulate concepts
Abstract thinking
Fluctuations in consciousness and disorientation. Also memory, language, sleep-wake disturbances
Delirium
Often precedes squamous cell carcinoma
Actinic keratosis
1° adrenocortical deficiency
Addison's disease
Polyostotic fibrous dysplasia, precocious puberty, café-au-lait spots, short stature, young girls
Albright's syndrome
↑ protein in CSF with only modest ↑ in cell count
Albuminocytologic dissociation seen in Guillain-Barré
Hereditary nephritis with nerve deafness
Alport's syndrome
Anti-basement membrane antibodies
Goodpasture's syndrome
Scleroderma (CREST)
Anticentromere antibodies
Anti-double-stranded DNA antibodies (ANA antibodies)
SLE (type III hypersensitivity)
Anti-epithelial cell antibodies
Pemphigus vulgaris
Antigliadin antibodies
Celiac disease
Drug-induced SLE
Antihistone antibodies
Anti-IgG antibodies
Rheumatoid arthritis
Antimitochondrial antibodies
1° biliary cirrhosis
Antineutrophil antibodies
Vasculitis
Antiplatelet antibodies
Idiopathic thrombocytopenic purpura
Arachnodactyly
Marfan's syndrome
Argyll Robertson pupil
Neurosyphilis
Cerebellar tonsillar herniation
Arnold-Chiari malformation
Aschoff bodies
Rheumatic fever
Atrophy of the mammillary bodies
Wernicke's encephalopathy
Auer rods
Acute myelogenous leukemia (especially the promyelocytic type)
Autosplenectomy
Sickle cell anemia
Babinski's sign
UMN lesion
Baker's cyst in popliteal fossa
Rheumatoid arthritis
Hyperreninemia
Bartter's syndrome
Basophilic stippling of RBCs
Lead poisoning
Becker's muscular dystrophy
Defective dystrophin; less severe than Duchenne's
LMN CN VII palsy
Bell's palsy
Multiple myeloma (kappa or lambda Ig light chains in urine), Waldenström's macroglobulinemia (IgM)
Bence Jones proteins
IgA nephropathy
Berger's disease
Defect in platelet adhesion
Bernard-Soulier disease
Bilateral hilar adenopathy, uveitis
Sarcoidosis
Birbeck granules on EM
Histiocytosis X (eosinophilic granuloma)
Bloody tap on LP
Subarachnoid hemorrhage
"Blue bloater"
Chronic bronchitis
Blue-domed cysts
Fibrocystic change of the breast
Blue sclera
Osteogenesis imperfecta
Tetralogy of Fallot; RVH
Boot-shaped heart on x-ray
PIP swelling 2° to osteophytes
Bouchard's nodes found in Osteoarthritis
Boutonnière deformity
Rheumatoid arthritis
Branching rods in oral infection
Actinomyces israelii
"Brown tumor" of bone
Hemorrhage causes brown color of osteolytic cysts: 1. Hyperparathyroidism 2. Osteitis fibrosa cystica (von Recklinghausen's disease)
Brushfield's spots
Down syndrome
X-linked agammaglobulinemia
Bruton's disease
Posthepatic venous thrombosis
Budd-Chiari syndrome
Small/medium-artery vasculitis
Buerger's disease
8:14 translocation; associated with EBV
Burkitt's lymphoma (c-myc activation)
Burton's lines
Lead poisoning
C-ANCA, P-ANCA
Wegener's granulomatosis, polyarteritis nodosa
Café-au-lait spots on skin
Neurofibromatosis
Gas emboli
Caisson disease
Calf pseudohypertrophy
Duchenne's muscular dystrophy
Call-Exner bodies
Granulosa-theca cell tumor of the ovary
Cardiomegaly with apical atrophy
Chagas' disease
Cerebriform nuclei
Mycosis fungoides (cutaneous T-cell lymphoma)
Chagas' disease
Trypanosome infection
Chancre
1° syphilis (not painful)
Haemophilus ducreyi
Chancroid (painful)
Multiple sclerosis (nystagmus, intention tremor, scanning speech), cholangitis (jaundice, RUQ pain, fever)
Charcot's triad
Charcot-Leyden crystals
Bronchial asthma (eosinophil membranes)
Phagocyte deficiency
Chédiak-Higashi disease
Cherry-red spot on macula
Tay-Sachs, Niemann-Pick disease, central retinal artery occlusion
Central apnea in CHF and ↑ intracranial pressure
Cheyne-Stokes respirations
Endometriosis (frequently involves both ovaries)
"Chocolate cysts"
Predisposition to gastric carcinoma
Chronic atrophic gastritis
facial muscle spasm upon tapping
Chvostek's sign due to hypocalcemia
DES exposure in utero
Clear cell adenocarcinoma (CCA) of the vagina and cervix
Clue cells
Gardnerella vaginitis
Codman's triangle on x-ray
Osteosarcoma
Cold agglutinins
Mycoplasma pneumoniae, infectious mononucleosis
Condylomata lata
2° syphilis
Continuous machinery murmur
Patent ductus arteriosus
Debranching enzyme deficiency
Cori's disease
Cotton-wool spots
Chronic hypertension
Cough, conjunctivitis, coryza
Measles
Councilman bodies
Toxic or viral hepatitis
Cowdry type A bodies
Herpesvirus
Rapidly progressive crescentic glomerulonephritis
Crescents in Bowman's capsule
Congenital unconjugated hyperbilirubinemia
Crigler-Najjar syndrome
Acute gastric ulcer associated with severe burns
Curling's ulcer
Currant-jelly sputum
Klebsiella
Curschmann's spirals
Bronchial asthma (whorled mucous plugs)
Acute gastric ulcer associated with CNS injury
Cushing's ulcer
D-dimers
DIC
basal ganglia disorder--rigidity, resting tremor, bradykinesia
Depigmentation of neurons in
Parkinson's disease
Dermatitis, dementia, diarrhea
Pellagra (niacin, vitamin B3 deficiency)
Diabetes insipidus + exophthalmos +
Hand-Schüller-Christian disease
Dog or cat bite
Pasteurella multocida
Donovan bodies
Granuloma inguinale
Congenital conjugated hyperbilirubinemia (black liver)
Dubin-Johnson syndrome
Deleted dystrophin gene (X-linked recessive)
Duchenne's muscular dystrophy
Eburnation
Osteoarthritis (polished, ivory-like appearance of bone)
Rocker-bottom feet, low-set ears, heart disease
Edwards' syndrome: Trisomy 18
Late cyanosis shunt (uncorrected L → R shunt becomes R → L shunt)
Eisenmenger's complex
Elastic skin
Ehlers-Danlos syndrome
Superior trunk brachial plexus injury ("waiter's tip")
Erb-Duchenne palsy
Erythema chronicum migrans
Lyme disease
Proximal tubular reabsorption defect
Fanconi's syndrome
Ferruginous bodies
Asbestosis
Colon polyps with osteomas and soft tissue tumors
Gardner's syndrome
Glucocerebrosidase deficiency
Gaucher's disease
Ghon focus
1° TB
Benign congenital unconjugated hyperbilirubinemia
Gilbert's syndrome
Defect in platelet aggregation
Glanzmann's thrombasthenia
Autoantibodies against alveolar and glomerular basement membrane proteins
Goodpasture's syndrome
Duchenne's (use of patient's arms to help legs pick self off the floor)
Gowers' maneuver
Idiopathic polyneuritis
Guillain-Barré syndrome
β-thalassemia, sickle cell anemia (extramedullary hematopoiesis)
"Hair-on-end" appearance on x-ray
Chronic progressive histiocytosis
Hand-Schüller-Christian disease
Thalassemia major
HbF
HbS
Sickle cell anemia
hCG elevated
Choriocarcinoma, hydatidiform mole (occurs with and without embryo)
Heberden's nodes
Osteoarthritis (DIP swelling 2° to osteophytes)
Heinz bodies
G6PD deficiency
Hypersensitivity vasculitis associated with hemorrhagic urticaria and URIs
Henoch-Schönlein purpura
Heterophil antibodies
Infectious mononucleosis (EBV)
High-output cardiac failure (dilated cardiomyopathy)
Wet beriberi (thiamine, vitamin B1 deficiency)
HLA-B27
Reiter's syndrome, ankylosing spondylitis
HLA-DR3 or -DR4
Diabetes mellitus type 1 (caused by autoimmune destruction of β cells)
Homer Wright rosettes
Neuroblastoma
Interstitial fibrosis
Honeycomb lung on x-ray
Splenectomy (or nonfunctional spleen)
Howell-Jolly bodies
Caudate degeneration (autosomal dominant)
Huntington's disease
Hyperphagia + hypersexuality + hyperorality + hyperdocility
Klüver-Bucy syndrome (amygdala)
Hyperpigmentation of skin
1° adrenal insufficiency (Addison's disease)
Hypersegmented neutrophils
Macrocytic anemia
Hypertension + hypokalemia
Conn's syndrome
Hypochromic microcytosis
Iron deficiency anemia, lead poisoning
Increased α-fetoprotein in amniotic fluid/maternal serum
Anencephaly, spina bifida (neural tube defects)
Increased uric acid levels
Gout, Lesch-Nyhan syndrome, myeloproliferative disorders, loop and thiazide diuretics
Intussusception
Adenovirus (causes hyperplasia of Peyer's patches)
Janeway lesions
Endocarditis
Jarisch-Herxheimer reaction
Syphilis—overaggressive treatment of an asymptomatic patient that causes symptoms due to rapid lysis
Neutrophil chemotaxis abnormality
Job's syndrome
AIDS in MSM (men who have sex with men)
Kaposi's sarcoma
Dynein defect
Kartagener's syndrome
Kayser-Fleischer rings
Wilson's disease
Keratin pearls
Squamous cell carcinoma
Kimmelstiel-Wilson nodules
Diabetic nephropathy
Bilateral amygdala lesions
Klüver-Bucy syndrome
Koilocytes
HPV
Koplik spots
Measles
Gastric adenocarcinoma with ovarian metastases
Krukenberg tumor
Kussmaul hyperpnea
Diabetic ketoacidosis
Lens dislocation + aortic dissection + joint hyperflexibility
Marfan's syndrome (fibrillin deficit)
HGPRT deficiency
HGPRT (hypoxanthine-guanine phosphoribosyl transferase) deficiency
Lines of Zahn
Arterial thrombus
Lisch nodules
Neurofibromatosis (von Recklinghausen's disease)
Low serum ceruloplasmin
Wilson's disease
Lucid interval
Epidural hematoma
"Lumpy-bumpy" appearance of glomeruli on immunofluorescencee
Poststreptococcal glomerulonephritis
Lytic bone lesions on x-ray
Multiple myeloma
Mallory bodies
Alcoholic liver disease
Esophagogastric lacerations
Mallory-Weiss syndrome
Muscle phosphorylase deficiency
McArdle's disease
McBurney's sign
Appendicitis
MLF syndrome (INO)
Multiple sclerosis
Monoclonal antibody spike
Multiple myeloma (called the M protein; usually IgG or IgA), MGUS (monoclonal gammopathy of undetermined significance), Waldenström's (M protein = IgM) macroglobulinemia
Myxedema
Hypothyroidism
Necrotizing vasculitis (lungs) and necrotizing glomerulonephritis
Wegener's and Goodpasture's (hemoptysis and glomerular disease)
Negri bodies
Rabies
Nephritis + cataracts + hearing loss
Alport's syndrome
Sphingomyelinase deficiency
Niemann-Pick disease
No lactation postpartum
Sheehan's syndrome (pituitary infarction)
Nutmeg liver
CHF
Occupational exposure to asbestos
Malignant mesothelioma
"Orphan Annie" nuclei
Papillary carcinoma of the thyroid
Osler's nodes
Endocarditis
Painless jaundice
Pancreatic cancer (head)
Palpable purpura on legs and buttocks
Henoch-Schönlein purpura
Bronchogenic apical tumor associated with Horner's syndrome
Pancoast's tumor
Pannus
Rheumatoid arthritis
Nigrostriatal dopamine depletion
Parkinson's disease
Periosteal elevation on x-ray
Pyogenic osteomyelitis
Benign polyposis
Peutz-Jeghers syndrome
Penile fibrosis
Peyronie's disease
Philadelphia chromosome (t(9;22); bcr-abl hybrid)
CML (may sometimes be associated with AML)
Emphysema (centroacinar [smoking], panacinar [α1-antitrypsin deficiency])
"Pink puffer"
Esophageal webs with iron deficiency anemia
Plummer-Vinson syndrome
Gout (MP joint of hallux)
Podagra
Minimal change disease
Podocyte fusion
Polyneuropathy, cardiac pathology, and edema
Dry beriberi (thiamine, vitamin B1 deficiency)
Polyneuropathy preceded by GI or respiratory infection
Guillain-Barré syndrome
Lysosomal glucosidase deficiency associated with cardiomegaly
Pompe's disease
Positive anterior "drawer sign"
Anterior cruciate ligament injury
Vertebral tuberculosis
Pott's disease
Pseudopalisade tumor cell arrangement
Glioblastoma multiforme
Pseudorosettes
Ewing's sarcoma
Rash on palms and soles
2° syphilis, Rocky Mountain spotted fever
Recurrent vasospasm in extremities
Raynaud's syndrome
Acute glomerulonephritis
RBC casts in urine
Recurrent pulmonary Pseudomonas and S. aureus infections
Cystic fibrosis
Red urine in the morning
Paroxysmal nocturnal hemoglobinuria
Reid index (increased)
Chronic bronchitis
Reinke crystals
Leydig cell tumor
Urethritis, conjunctivitis, arthritis
Reiter's syndrome
Renal cell carcinoma + cavernous hemangiomas + adenomas
von Hippel-Lindau disease
Renal epithelial casts in urine
Acute toxic/viral nephrosis
Rib notching
Coarctation of aorta
Congenital conjugated hyperbilirubinemia
Rotor's syndrome
Rouleaux formation (RBCs)
Multiple myeloma
Russell bodies
Multiple myeloma
S3
- Left-to-right shunt (VSD, PDA, ASD)
- Mitral regurgitation
- LV failure (CHF)
S4
- Aortic stenosis
- Hypertrophic subaortic stenosis
Schiller-Duval bodies
Yolk sac tumor
Cutaneous T-cell lymphoma
Sézary syndrome
Shwartzman reaction
Neisseria meningitidis
Signet-ring cells
Gastric carcinoma
Sipple's syndrome
MEN type IIa
Dry eyes, dry mouth, arthritis
Sjögren's syndrome
"Smudge cell"
CLL
Soap bubble on x-ray
Giant cell tumor of bone
Spike and dome on EM
Membranous glomerulonephritis
Spitz nevus
Benign juvenile melanoma
"Strawberry tongue"
Scarlet fever
String sign on x-ray
Crohn's disease
Subepithelial humps on EM
Poststreptococcal glomerulonephritis
Suboccipital lymphadenopathy
Rubella
Sulfur granules
Actinomyces israelii
Swollen gums, bruising, poor wound healing, anemia
Scurvy (ascorbic acid, vitamin C deficiency): vitamin C is necessary for hydroxylation of proline and lysine in collagen synthesis
Systolic ejection murmur (crescendo-decrescendo)
Aortic valve stenosis
t(14;18)
Follicular lymphomas (bcl-2 activation)
Tendon xanthomas (classically Achilles)
Familial hypercholesterolemia
Thumb sign on lateral x-ray
Epiglottitis (Haemophilus influenzae)
Thyroidization of kidney
Chronic bacterial pyelonephritis
"Tram-track" appearance on LM
Membranoproliferative glomerulonephritis
Trousseau's sign
Visceral cancer, pancreatic adenocarcinoma (migratory thrombophlebitis), hypocalcemia (carpal spasm)
Left supraclavicular node enlargement from metastatic carcinoma of the stomach
Virchow's node
Pulmonary embolism (blood stasis, endothelial damage, hypercoagulation)
Virchow's triad
Neurofibromatosis with café-au-lait spots
von Recklinghausen's disease
Osteitis fibrosa cystica ("brown tumor")
von Recklinghausen's disease of bone
PICA thrombosis
Wallenberg's syndrome
Adrenal hemorrhage associated with meningococcemia
Waterhouse-Friderichsen syndrome
Waxy casts
Chronic end-stage renal disease
WBC casts in urine
Acute pyelonephritis
WBCs in urine
Acute cystitis
Wermer's syndrome
MEN type I
Malabsorption syndrome caused by Tropheryma whippelii
Whipple's disease
Hepatolenticular degeneration
Wilson's disease
"Wire loop" appearance on LM
Lupus nephropathy
"Worst headache of my life"
Berry aneurysm—associated with adult polycystic kidney disease
Xanthochromia (CSF)
Subarachnoid hemorrhage
Xerostomia + arthritis + keratoconjunctivitis sicca
Sjögren's syndrome
Upper GI diverticulum
Zenker's diverticulum
Gastrin-secreting tumor associated with ulcers
Zollinger-Ellison syndrome