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77 Cards in this Set
- Front
- Back
OA vs. RA: which is symmetrical and which is asymmetrical? Which is autoimmune and which is wear-and-tear related?
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OA: wear and tear, asymmetrical
RA: autoimmune, symmetrical |
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What is the most common form of arthritis?
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OA
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OA vs. RA: which affects large weight bearing joints? Which affects smaller joints?
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OA: large joints (knees, hips, spine)
RA: small joints (hands and feet) |
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T or F: OA risk increases with age.
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true
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OA vs. RA: which produces synovial proliferation?
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RA
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How would x-rays differ in OA and RA?
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OA: narrowed joint space
RA: juxta-articular osteoporosis and bone erosions; joint effusion |
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RA or OA: which shows morning stiffness that improves throughout the day?
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RA
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What are some systemic symptoms of RA?
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fever, malaise, fatigue, lymphadenopathy, rheumatoid nodules, Sjogren’s syndrome, amyloidosis
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Synovitis, pannus formation, fibrous and bony ankylosis, joint deformities, and baker cysts are all symptoms of OA or RA?
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RA
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What is eburnation? Is this seen in OA or RA?
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exposed bone becomes polished; OA
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A systemic, chronic inflammatory disease characterized by progressive arthritis, production of rheumatoid factor, and extra-articular manifestations:
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RA
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OA or RA: subchondral bone sclerosis and cysts, loose bodies, bone spurs.
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OA
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OA or RA: affects females 20-50
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RA
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What are the possible genetic causes for RA?
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HLA-DR4 and DR1
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OA or RA: which is associated with "loose bodies" and osteophytes (bone spurs)?
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OA
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What is the term for arthritis due to infection? Which bacterium is most often associated with this kind of arthritis?
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suppurative arthritis; gonococci, staph, strep
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Where are rheumatoid nodules normally found?
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extensor surfaces of forearms or elbows
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Which form of arthritis usually displays large, tender, painful, swollen erythematous joints, and is monoarticular?
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suppurative arthritis
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In which arthritis will there be cloudy synovial fluid with high neutrophil count?
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suppurative arthritis
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What are the features of a ganglionic cyst?
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1. up to 1.5cm
2. in joint capsule or tendon sheath 3. benign 4. no communication with joint space 5. likely recurrence |
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What is the most common MD?
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Duchenne's
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What is lacking in Duchenne's MD?
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dystrophin
(hint: Duchenne's-Dystrophin-Disastrous) |
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What is the problem in Becker's MD?
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dystrophin size is altered
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Which MD has a slower progression and is more delayed: Becker's or Duchenne's?
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Becker's
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What gene is affected in X-linked MD? Which protein does this encode?
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Xp21 gene; encodes a 427kd protein
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Which MD has the following histopathology: variation in fiber size, increased number of internalized nuclei, degeneration of muscle fibers, regeneration of muscle fibers, and proliferation of endomysial connective tissue?
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x-linked MD
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Which MD is normal at birth, but begins to weaken by 5 y/o with death by early 20’s?
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x-linked MD
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Which ion channel myopathy shows the following: autosomal dominance, hypermetabolic state triggered by anesthesia, (halogens and succinylcholine), and mutation in sodium channels?
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malignant hyperpyrexia (malignant hyperthermia)
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What is Lambert-Eaton (LE) myasthenic syndrome? What is this commonly associated with?
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paraneoplastic disorder of the NMJ; small cell carcinoma of the lung
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MG or LE: which has increased contractions with repeated stimuli?
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Lambert-Eaton (LE)
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What disease presents with easy fatigability, ptosis, thymoma, and diplopia resulting from immune mediated injury?
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MG
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Antibodies are formed against what in MG?
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Ach receptors
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What is the treatment in MG?
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plasmapheresis; removing thymomas
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What is the most common form of inherited dwarfism?
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achondroplasia
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What is the inheritance pattern seen in achondroplasia?
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autosomal dominant
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Where is the mutation in achondroplasia? What does this do?
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mutation in fibroblast growth factor receptor 3 (FGFR3)->inhibited cartilage synthesis at epiphyseal growth plate, decreased endochondral bone formation and premature ossification of the growth plates
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Describe the bone structure in achondroplasia:
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long bones are short and thick, cranium and vertebrae are normal
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Briefly describe osteogenesis imperfecta (OI):
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hereditary defect that causes abnormal synthesis of type I collagen, leading to brittle bones
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What disease will display the following features: recurrent fractures, blue sclera, deafness, and hypermobility?
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OI
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Of the 4 types of osteogenesis imperfecta, which form is the most lethal?
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type II (causes stillbirth)
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Name the disease: localized disorder of bone remodeling resulting in excessive bone resorption followed by disorganized bone replacement, producing thick but weak bone that is susceptible to deformity and fracture.
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Paget's disease
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Describe the pattern seen in Paget's disease:
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Triphasic Pattern: osteolytic, mixed osteolytic-osteoblastic, osteosclerotic
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What population does Paget's disease mostly affect?
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those of European descent over 40 y/o
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What is the most common bone disease in the U.S.? Who does it target?
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osteoporosis; postmenopausal women and elderly
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Name the disease: decreased bone mass (ostopenia) resulting in thin fragile bones that are susceptible to fracture.
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osteoporosis
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What are the 2 forms of osteomyelitis?
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pyogenic and tuberculous
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What is the most common spread of pyogenic osteomyelitis?
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hematogenous (seeding of bone after infection)
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What bacteria are indicated in pyogenic osteomyelitis?
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Staph aureus, E coli, Streptococci, Gonococci, Haemophilus influenzae, Salmonella, Pseudomonas
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What are the clinical signs in pyogenic osteomyelitis?
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fever and leukocytosis, localized pain, erythema, and swelling
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What is the treatment for pyogenic osteomyeltis?
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antibiotics and surgical drainage
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Name the disease based on this characteristic: caseating granulomas with extensive destruction of the bones.
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tuberculous osteomyelitis
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What are the common sites for tuberculous osteomyelitis?
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thoracic and lumbar vertebrae (“Pott disease”)
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Tuberculous osteomyelitis is seen in what % of TB cases?
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1%
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What is the most common bone lesion?
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metastatic cancer (prostate, breast, lung, thyroid, kidney)
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Name the disease: malignant neoplasm of undifferentiated cells arising in marrow cavity.
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Ewing's Sarcoma
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Describe the genetics of Ewing's sarcoma:
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classic translocation t(11;22) which produces EWS-FLI1 fusion protein
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What populations are affected most by Ewing's sarcoma?
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males more than females, teenagers
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What is the most common soft tissue tumor of adulthood?
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lipoma
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What does a lipoma (fatty tumor) consist of?
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mature fat cells and delicate reticulin network with a surrounding capsule
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Where are lipomas normally found on the body? What populations?
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trunk or upper extremities in the subcutaneous region; middle-aged and elderly men and women
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What is the treatment for lipoma?
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excision
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What is one of the most common sarcomas of adulthood? What populations are seen?
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liposarcoma; 40's-60's
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Where are liposarcomas found?
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deep soft tissues of proximal extremities and retroperitoneum
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What are some microscopic findings in a liposarcoma?
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well-differentiated, myxoid, round cell and pleomorphic variants; lipoblasts with small lipid vacuoles
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What is the most common type of soft tissue sarcoma? Which of these is most common?
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malignant fibrous histiocytoma (MFH); Storiform-pleomorphic
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What are some microscopic findings in an MFH?
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swirling (storiform) pattern, plump spindle cells
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Where are MFH normally found? What population?
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deep soft tissues of extremities; peak in 7th decade
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Name the disease: presence of metaplastic bone in soft tissue (musculature); usually in athletic adults/young adults following trauma.
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Myositis Ossificans
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How can Myositis Ossificans be differentiated from a neoplasm?
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in MO, bone matures peripherally, not centrally
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How can MO be treated?
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excision
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Is this early or late MO: circumscribed, full → painless, hard, well-demarcated?
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late
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What skin lesion is a benign, round, brownish purple growth with an unknown etiology?
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dermatofibroma
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Which type of OI shows little progression after puberty?
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type I
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X-ray findings in osteopetrosis?
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Erlenmeyer flask”-shaped deformity
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Paget's disease would show elevation of what lab test?
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alk phos
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T or F: Paget's disease can have cardiac sequelae?
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true
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What is the most common organism in osteomyelitis?
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s. aureus
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