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111 Cards in this Set

  • Front
  • Back
Hypospadias
(a) describe
(b) associations
(c) complications
(a) urethra opens onto ventral surface of penis
(b) poorly developed penis that curves ventrally (chordee)
(c) infertility; increase risk of UTI's
Epispadias
(a) describe
(b) associations
(c) complications
(a) urethra opens onto dorsal surface
(b) extrophy of bladder
(c) infertility
Phimosis
(a) describe
(b) complications
(c) treatment
(a) prepuce orifice too small to be retracted normally
(b) hygiene interference; predispose to infx; if foreskin retracted over glans may lead to urethral constriction (paraphimosis)
(c) circumcision
Bowen's disease
(a) description
(b) epidemiology
(c) gross
(d) microscopic
(e) outcome
(a) penile carcinoma in situ
(b) mend>35; can be assoc w/visceral malignancy
(c) thick, ulcerated plaque usually on shaft or scrotum
(d) SCC in situ
(e) <10% progress to invasive SCC
Squamous Cell carcinoma of penis
(a) epidemiology
(b) clinical presentation
(c) risk factors
(d) gross
(e) outcomes
(a) 1% of cancer in men; 40-70YO; rare in circumsized men
(b) slow growing; not painful
(c) HYPV 16,18
(d) plaque progressing to ulcerated papule or fungating growth
(e) mets can go to local LN
Erythroplasia of Queyrat; appearance
Red velvety plaques usually involving glans; otherwise similar to Bowen's
Bowenoid papulosis; appearance, epidemiology, outcome
Multiple papular lesions; younger age group; usually not invade
Peyronie's Disease
Bent penis due to acquired fibrous tissue formation
Prostate adenocarcinoma
(a) epidemiology
(b)clinical presentation/lobe of prostate involved?
(c) diagnosis
(d) metastasis
(e) treatment
(a) >50YO; AA>caucasians
(b) urinary problems ; assoc w/posterior lobe enlargement
(c) PSA (incr total PSA, w/ decr fraction of free PSA); DRE
(d) mets via lymphatic or hematogenous route (bone w/osteoblastic mets indicated by back pain and incr alkP)
(e) surgery, rad, hormonal modalities
Benign prostatic hyperplasia
(a) epidemiology
(b) possible etiology/lobe of prostate involved?
(c) clinical presentation
(d) complications
(e) diagnosis
(a) common in M>50
(b) hyperplasia; possible due to DHT; middle and lateral lobes hyperplasia
(c) may narrow urethral canal; incr urinary frequency, nocturia, difficulty starting and stopping stream
(d) distention and hypertrophy of bladder, hydronephrosis and UTI's
(e) incr free PSA
Acute prostatitis
(a) most common pathogens
(b) spread via?
(a) same as UTI (E coli most common)
(b) direct extension or lymphatic/hematogenous
Chronic prostatitis
(a) common causes
(b) presentation
(a) bacterial and nonbacterial
(b) asymptomatic or present with lower back pain and urinary sx
Cryporchidism
(a) cause
(b) most common location
(c) complications
(a) failure of normal testes descent
(b) inguinal canal (more often on right); can be bilateral
(c) bilateral (infertility); incr incidence of testicular cancer
Torsion
(a) clinical presentation
(b) complications
(a) sudden onset testicular pain, and loss of cremasteric reflex
(b) compromise arterial/venous drainage (infarction)
Testicular hydrocoele
(a) description
(b) precipitating events
(a) patency of processus vaginalis remains
(b) inflammatory causes (epididymitis)
Testicular varicocoele
(a) cause
(b) clinical presentation
(c) complications
(a) dilatations of tributaries of testicular vein and pampiniform plexus "bag of worms"
(b) varicosities seen when standing but disappear when sitting down
(c) can cause infertility
Spermatocoele
Dilated epididymal duct
Seminoma
(a) epidemiology
(b) histology
(c) prognosis
(d) treatment
(a) 15-35YO M (most common testicular tumor)
(b) large cells in lobules w/"fried egg appearance"
(c) excellent (late mets)
(d) radiosensitive
Embryonal carcinoma of testes
(a) clinical presentation
(b) histology
(c) outcome
(d) diagnosis
(a) pain
(b) often glandular/papillary; can differentiate to other tumor
(c) malignant; high mortality; less radiosensitive (may require orchiectomy)
(d) incr serum AFP
Choriocarcinoma
(a) epidemiology
(b) clinical presentation
(c) markers
(d) outcome
(e) treatment
(a) 15-25YO
(b) gynecomastia' testicular enlargement
(c) elevated hCG
(d) disseminates hematogenously (lungs, liver, brain)
(e) orchiectomy or chemo
Yolk sac (endodermal sinus) tumor
(a) epidemiology
(b) serum markers
(c) histology
(a) rare; most common in children and infants
(b) high alpha fetoprotein (AFP)
(c) Schiller-Duval bodies, primitive glomeruli
Testicular teratoma
(a) epidemiology
(b) clinical presentation
(c) histology
(d) prognosis
(e) treatment
(a) any age but mostly infants/children
(b) testicular mass
(c) variety of tissues
(d) mature teratoma often malignant
(e) orchiectomy followed by chemo and rad
Leydig cell tumor
(a) clinical presentation
(b) unilateral/bilateral
(c) treatment/prognosis
(a) testicular enlargement; often androgen producing (gynecomastia in men precocious puberty in boys)
(b) unilateral
(c) usually curative w/surgery
Sertoli cell tumor
(a) clinical presentation
(b) unilatera/bilateral
(c) outcome
(a) testicular enlargement
(b) unilateral
(c) usually benign
Testicular lymphoma
(a) epidemiology
Most common testicular cancer in elderly men
Klinefelter's Syndrome
(a) genetics
(b) pathophys
(c) clinical presentation
(a) XXY; inactivated X chromosome (barr body)
(b) dysgenesis of seminiferous tubules, decr inhibin, incr FSH. Abnormal leydig cell fct; decr testosteron, incr LH and estrogen
(c) hypogonadism, eunuchoid body shape, tall long extremities, gynecomastia, female hair distribution
Turner's Syndrome
(a) genetics
(b) clinical presentation
(c) pathophys
(a) XO
(b) short stature; ovarian dysgenesis (streaks); webbed neck; preductal coarctation of aorta; most common cause of primary amenorrhea
(c) decr estrogen leads to incr LH and FSH
Double Y males clinical presentation
Phenotypically normal; tall; severe acne; antisocial behavior in 1-2% of men; normal fertility
Female pseudohermaphrodite
(a) Genetics
(b) pathophys/cause
(c) internal/external genitalia/presentation
(a) XX
(b) excessive/inappropriate androgens during early gestation (congenital adrenal hyperplasia, exogenous)
(c) ovaries but virilized/ambiguous external genitalia
Male pseudohermaphrodite
(a) Genetics
(b) pathophys/cause
(c) internal/external genitalia/presentation
(a) XY
(b) most common form is androgen insensitivity syndrome
(c) testes but female external genitalia (or ambiguous)
True hermaphrodite
(a) genetics
(b) internal/external genitalia
(a) either 46XX or 46XY
(b) both ovaries and testes; ambiguous genitalia
Androgen insensitivity syndrome
(a) genetics
(b) cause/pathophys
(c) internal/external genitalia/clinical presentation
(d) sex hormone levels
(a) 46XY
(b) defective androgen receptor
(c) normal appearing female; female external genitalia w/blunt vagina; uterus and uterine tubes absent; testes
(d) levels of testosterone, estrogen, and LH high
5alpha reductase deficiciency
(a) defect
(b) clinical presentation
(c) sex hormone levels
(a) unable to convert testosterone to DHT
(b) ambiguous genitalia until puberty when incr testosterone causes masculinization
(c) testosterone/estrogen levels normal; LH is normal or high
Common cause of recurrent miscarriages: 1st weeks
Low progesterone level (no response to beta hCG)
Common cause of recurrent miscarriage: 1st trimester
Chromosomal abnormalities (robertsonian translocation)
Common cause of recurrent miscarriage: 2nd trimester
Bicornate uterus
Preeclampsia triad
HTN, proteinuria, edema after 20wk gestation
Eclampsia
HTN, proteinuria, edema, seizures
Etiology of preclampsia
Placental ischemia (lack of trophoblast invasion of spiral arteries in myometrium) causing elaboration of factors leading to altered maternal endothelial fct (incr vascular tone, incr vascular permeability, coagulopathy)
Complications of preeclampsia
Hemolysis, Elevated LFT's, Low platelets
Clinical features of preeclampsia
HA, blurred vision, abd pain, edema, altered mentation, hyperreflexia
Lab values in preeclampsia
Thrombocytopenia, hyperuricemia
Treatment of preeclampsia
Delivery of fetus as soon as viable; bed rest, salt restriction, monitor/treat HTN
IV mgsulfate and diazepam to prevent and treat seizures
Abruptio placenta
(a) description
(b) presentation
(c) complications
(d) risk factors
(a) premature detachment of placenta from implantation site
(b) painful bleeding in 3rd trimester
(c) fetal death; DIC
(d) incr risk w/smoking, HTN, cocaine
Placenta accreta
(a) description
(b) presentation
(c) complications
(d) risk factors
(a) defective decidual layer; placenta attached to myometrium
(b) massive bleeding after delivery
(c) see above
(d) prior C section, PID
Placenta previa
(a) description
(b) presentation
(c) complications
(d) risk factors
(a) attachment of placenta to lower uterine segment
(b) painless bleeding in any trimester
(c) may occlude internal os
(d) prior C section
Ectopic pregnancy
(a) clinical presentation/lab findings
(b) most common site
(c) risk factors
(a) pain without bleeding; incr hCG; presents like appendicitis
(b) fallopian tubes
(c) PID
Polyhydramnios
(a) define
(b) associations/cause
(a) >1,5-2L of amniotic fluid
(b) esophageal/duodenal atresia (inability to swallow fluid); anencephaly
Oligohydramnios
(a) define
(b) cause
(c) result
(a) <0.5L amniotic fluid
(b) bilateral renal agenesis or posterior urethral valves; inability to secrete urine
(c) Potter's syndrome
Condyloma acuminatum
(a) presentation
(b) histology
(c) distribution
(d) etiology
(e) complications
(a) warts
(b) koilocytes, acanthosis, hyperkeratosis, parakeratosis
(c) vulva, perineum, vagina,cervix
(d) HPV 6,11 association
(e) incr risk ofcervical carcinoma
Papillary hidradenoma
(a) description
(b) distribution
(a) benign tumor similar to intraductal papilloma of breast
(b) occur along milk line
Extramammary Paget disease of vulva
(a) presentation
(b) histology
(c) distribution
(d) assoc w/underlying tumor?
(a) erythematous, crusted rash
(b) intraepidermal malignant cells w/pagetoid spread
(c) labia majora
(d) not assoc w/underlying tumor
Candida vulvovaginitis
(a) description
(b) distribution
(c) risk factors
(a) erythema, thick white discharge
(b) vulva and vagina
(c) common; esp in diabetics and after antibiotic use
Embryonal Rhabdomyosarcoma
(a) epidemiology
(b) gross description
(c) histology
(a) rare; affect female infants and young children
(b) grapelike, soft tissue mass protruding from vagina
(c) spindle cell tumor; + desmin (skeletal muscle origin)
Clinical presentation of cervical carcinoma
Postcoital bleeding, dyspareunia, discharge
May be asymptomatic
Endometriosis
(a) description
(b) pathology
(c) clinical presentation
(d) complications
(a) endometrial glands outside uterus
(b) red brown nodules (powder burns); ovarian "chocolate cysts"
(c) severe menstrual related pain; rectal pain and constipation
(d) may result in infertility
Endometritis
(a) description
(b) pathology
(c) clinical
(a) ascending infection of cervix
(b) ureaplasma, peptostrep, gardnerella, Bacteriodes, GBS, chlamydia
(c) assoc w/pregnancy or abortions; assoc w/PID and IUD's
Adenomyosis
Presence of endometrium within myometrium
Leiomyoma
(a) description
(b) pathology
(c) clinical
(d) complications
(a) benign smooth muscle tumor; grows in resp to estrogen; most common of all tumors
(b) well circumscribed; "whorled" white tan mass
(c) menorrhagia; abdominal mass; pelvic/back pain or suprapubic discomfort
(d) infertility; iron deficiency anemia (bleeding)
Leimyosarcoma
(a) description
(b) epidemiology
(c) clinical presentation
(a) highly aggressive bulky irregular shaped tumor w/necrosis and hemorrhage
(b) incr incidence in blacks
(c) may protrude from cervix and bleed
Gynecological tumor incidence and prognosis(endo, ovar, cerv)
Incidence: endo>ovar>cerv
Worst prognosis: ovarian>cervical>endometrial
Sex hormone levels in premature ovarian failure
Decr estrogen
Incr LH and FSH
Endometrial hyperplasia
(a) describe
(b) etiology
(c) clinical presentation
(d) risk factors
(a) abnormal endometrial gland prolif
(b) usually excess estrogen
(c) postmenopausal vaginal bleeding
(d) anovulatory cycles, HRT, PCOS, granulosa cell tumor
Endometrial carcinoma
(a) epidemiology
(b) clinical presentation
(c) gross path
(d) micro
(e) risk factors
(f) most important prognostic factor
(a) most common gynecological malignancy; peak at 55-65
(b) vaginal bleeding; typically preceded by endometrial hyperplasia
(c) tan polypoid mass
(d) endometriod adenocarcinoma
(e) unopposed estrogen; obesity; diabetes; HTN; nulliparity; late menopause
(f) myometrial invasion (stage)
Polycystic ovary disease
(a) presentation
(b) lab/path
(c) etiology
(d) treatment
(a) young, obese, hirsute females of reproductive age; oligomemnnorhea
(b) bilaterally enlarged, cystic ovaries
Elevated LH, low FSH, high testosterone
(c) incr LH stimulation leads to incr androgen synth
(d) wt loss, OCP's, gonadotropin analogs, clomiphene or surgery
Cystadenoma
(a) description
(b) pathology
(a) most common benign ovarian tumor
(b) unilocular cyst w/simple serous or mucinous lining
Follicular cyst
(a) desciption
(b) associations
Distention of unruptured graafian follicle
(b) hyperestrinism and endometrial hyperplasia
Corpus luteum cyst complications
Hemorrhage into persistant corpus luteum; menstrual irregularity
Theca lutein cyst
(a) presentation
(b) etiology
(c) associations
(a) often bilateral/multiple cysts
(b) gonadotropin stimulation
(c) choriocarcinoma and moles
"chocolate cyst"
Ovarian endometriosis
Teratoma
(a) epidemiology
(b) lab/path
(c) treatment
(a) 90% of all germ cell tumors; immature teratoma aggressivel malignant; mature benign
(b) contain 2-3 germ layers; immature contains primitive cells
(c) treatment
Dysgerminoma
(a) epidemiology
(b) lab/pathology
(c) risk factors
(d) treatment
(e) tumor marker
(a) mainly adults
(b) sheets of uniform cells (same as male seminoma)
(c) Turner's, pseudohermaphrotidism
(d) radiosensitive, so good prognosis
(e) hCG?
Choriocarcinoma
(a) clinical presentation
(b) tumor marker
(c) histology
(d) associations
(e) treatment
(a) malignant
(b) beta hCG
(c) large, hyperchromatic syncitiotrophoblastic cells
(d) incr frequency of theca-lutein cysts
(e) responsive to chemo
Yolk sac tumor: tumor marker
AFP
Granulosa cell tumor
(a) clinical presentation
(b) microscopic
(c) complications
(a) produces estrogen and can produce precocious puberty, irregular menses, or dysfunctional uterine bleeding
(b) polygonal tumor cells w/follicle like structures (Call Exner bodies-small follicles filled w/eosinophilic secretions)
(c) endometrial hyperplasia/cancer
Sertoli Leydig cell tumor
(a) clinical presentation
(a) androgen producing tumor; presents w/virilization in females
Hydatidiform mole
(a) clinical presentation
(b) serum markers
(c) treatment
(a) "size greater than date"; vaginal bleeding; passive of edematous grape like tissue
(b) beta hCG
Partial hydatidiform mole
(a) Karyotype
(b) hCG
(c) uterine sz
(d) convert to choriocarcinoma
(e) fetal parts
(a) 69XXY (2 sperm +1egg)
(b) incr
(c) nc
(d) rare conversion
(e) yes
Complete Hydatidiform mole
(a) Karyotype
(b) hCG
(c) uterine sz
(d) convert to choriocarcinoma
(e) fetal parts
(a) 46XX(or XY) both paternal
(b) highly elevated
(c) incr
(d) 2%
(e) no
Struma ovarii
Teratoma w/functional thyroid tissue (can present as hyperthyroidism)
Clear cell adenocarinoma (vagina) risk factor
Affect women who had exposure to diethylstilbestrol
Serous cystadenoma
(a) epidemiology
(b) presentation
(c) micro
(a) 20% of ovarian tumors
(b) frequently bilateral,
(c) lined w/fallopian tube like epithelium
General ovarian cancer tumor marker
CA-125
Genetic risk factors for ovarian cancer
BRCA1, HNPCC
Serous cystadenocarcinoma
(a) epidemiology
(b) presentation
(c) histology
(a) 50% of all ovarian tumors
(b) frequently bilateral
(c) psammoma bodies
Mucinous cystadenocarcinoma
(a) possible serious consequence
(b) route of spread
(a) pseudomyxoma peritonei-intraperitoneal accumulation of nmucinous material from ovarian tumor
(b) direct pelvic cavity seeding (like serous)
Brennar tumor
Benign ovarian tumor (bladder histology)
Ovarian fibroma
(a) histo
(b) Meig's syndrome
(a) bundles of spindle shaped fibroblasts
(b) Triad of ovarian fibroma, ascities, hydrothorax; pulling sensation in groin
Krukenberg tumor
GI malignancy that mets to ovaries causing mucin secreting sigment cell adenocarcinoma
Fibroadenoma of breast
(a) characteristics
(b) epidemiology
(c) gross histo
(d) micro histo
(e) risk for malignancy?
(a) small, mobile, firm w/sharp borders; incr sz and tenderness w/estrogen
(b) most common tumor in <25YO
(c) round/encapsulated
(d) glandular epithelial lined spaces w/fibroblastic stroma
(e) no
Intraductal papilloma
(a) characteristics
(b) epidemiology
(c) gross histo
(d) micro histo
(e) risk for malignancy?
(a) small tumor in lactiferous ducts; typically beneath areola; serous or bloody nipple discharge
(b) 20-50YO
(c) small, usually close to nipple
(d) multiple papillae
(e) slight incr
Phyllodes tumor
(a) characteristics
(b) epidemiology
(c) gross histo
(d) micro histo
(e) risk for malignancy?
(a) Large, bulky mass of CT and cysts leaflike" projections
(b) 6th decade
(c) irregular mass; often fungating or ulcerated
(d) myxoid stroma w/anaplasia
(e) some may become malignant
Risk factors for carcinoma of breast
Incr age
Nulliparity
Family hx
Early menarche
Late menopause
Fibrocystic disease
Previous hx
Obesity
High fat diet
What is the most important prognostic factor for breast cancer?
Axillary lymph node involvement
BRCA1
100% lifetime risk for breast cancer
Incr risk for ovarian CA (men at incr risk for prostate)
BRCA2
Incr incidence of breast CA only
Ductal carcinoma in situ
Fills ductal lumen
Invasive ductal carcinoma in situ
(a) characteristics
(b) epidemiology
(c) prognosis
(a) firm, fibrous mass; small glandular, duct like cells; foci of necrosis and calcification common
(b) most common breast CA
(c) worst and most invasive
Protein/receptor changes associ w/breast cancer
Overexpression of estrogen/progesterone rec
Overexpression of erb-2/Her-2( EGF receptor)
Invasive lobular carcinoma of the breast
(a) presentation
(b) gross
(c) histology
(d) tumor markers?
(a) often multiple/bilateral
(b) rubbery and ill defined
(c) small cells may be arranged in rows/rings; arise from terminal ductules
(d) assoc w/incr estrogen receptors
Medullary carcinoma of the breast
(a) gross
(b) micro
(c) prognosis
(a) fleshy mass
(b) large, pleomorphic cells jw/lyphocytic infiltrate
(c) good
Comedocarcinoma
(a) gross
(b) micro
(a) gocus of increased consistency in breast tissue
(b) typical duct epithelial cells proliferate and fill ducts;caseous necrosis (may discharge from nipple)
Paget disease of breast
(a) epidemiology/prognosis
(b) gross
(c) histo
(a) older women; poor prognosis
(b) skin of nipple and areola ulcerated/oozing
(c) ductal carcinoma (involving areolar skin) and large, hyperchromatic "paget cells"
P'eau D'orange
Dermal lymphatic invasion by breast cancer
Colloid (mucinous) carcinoma
(a) epidemiology
(b) prognosis
(c) gross
(c) histo
(a) older women
(b) slow growing better prognosis than ductal
(c) soft, large, gelatinous
(d) islands of tumor cells w/mucin
Fibrocystic disease
(a) description/epidemiology
(b) clinical presentation
(c) risk to carcinoma
(a) most common cause of breast lumps from age 25 to menopause
(b) premenstrual brast pain and multiple lesions
(c) usually not (except with epithelial hyperplasia histo type)
4 histologic types of fibrocystic disease
(1) fibrosis-hyperplasia of breast stroma
(2) cystic-fluid filled, blue dome
(3) sclerosing adenosis-incr acini and intralobular fibrosis
(4) epithelial hyperplasia-incr number of epithelial cell layers in terminal duct lobule (incr risk of carcinoma w/atypical cells)
Acute mastitis
(a) describe
(b) usually pathogens
(c) treatment
(a) fissures in nipples during nursing predispose to infx; breast abscess
(b) S aureus and strep
(c) Abs and surgical drainage
Fat necrosis of breast
(a) presentation
(b) cause
(a) benign, painless lump
(b) result from injury to breast tissue
Mammary duct ectasia (plasma cell mastitis)
(a) epidemiology
(b) clinical presentation
(a) 5th decade in multiparous women
(b) pain, redness, induration around areola w/thick secretion; usually unilateral
Skin fixation, nipple retraction, axillary lymphadenopathy can occur (distinguish from malignancy)
Gynecomastia causes
(a) hyperestrogenism (cirrhosis, testicular tumor, puberty, old age)
(b) Klinefelter's
(c) drugs (estrogen, mairjuana, heroin, psycoactive drugs, spironolactone, digitalis, cimetidine, alcohol, ketoconazole)