Tulane (HIGH YIELD) Flashcards

1
Q

What gestational structure secretes b-HCG?

A

Syncytiotrophoblasts (from outer layer of chorionic villi)

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2
Q

Presentation and most common cause of hematosalpinx

A

Severe abd pain 6 wks post last menstrual period; tubular ectopic pregnancy (rupture leads to massive intraperitoneal hemorrhage)

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3
Q

Preeclampsia symptom requirements

A

Proteinuria, HTN

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4
Q

TORCH infections

A

Toxoplasmosis, Other (syphilis, varicella, parvovirus, HIV, but also listerosis and TB), Rubella, CMV, Herpes

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5
Q

Syphilis treatment, broadly

A

Penicillin

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6
Q

What differentiates borderline ovarian tumors from benign or malignant?

A

Epithelial proliferation, but not invasion

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7
Q

What is Meigs syndrome?

A

Ovarian fibroma + pleural effusion, ascites

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8
Q

High risk HPV proteins and effects

A

E6: incr. degradation of p53 interrupts cell death and DNA repair
E7: binds Rb, causing incr. proliferation

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9
Q

Haplotype(s) associated with (type I) diabetes

A

HLA DR3/4 (both)

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10
Q

Autoantibodies associated with Type I diabetes

A

GAD65, ICA

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11
Q

Glucose-induced insulin secretion pathophys

A

Glucose enters pancreatic cell via GLUT2 transporter, glycolysis (glucokinase, etc) leads to incr. ATP, closing K+ channels, causing depolarization, which then opens voltage-gated Ca++ channel, leading to calcium influx which prompts insulin secretion

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12
Q

Why is the inhibin A level important for prenatal screening?

A

Down’s syndrome

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13
Q

Latency location of HSV-1

A

Trigeminal ganglia

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14
Q

Latency location fo HSV-2

A

Lumbosacral (dorsal root) ganglia

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15
Q

2 types of fibrocystic breast changes (incl. histopathology)

A
  • Non-proliferative (no incr. risk of cancer): fibrosis, cysts, apocrine metaplasia (not unique), adenosis (just plain old regular adenosis)
  • Proliferative (incr. risk of cancer): hyperplasia (atypical is worse), sclerosing adenosis (~ “complex sclerosing lesion”), small duct papillomas
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16
Q

Medullary breast cancer genetics

A

BRCA1 (occurs in younger women)

17
Q

Breast tumor(s) that lack E cadherin

A

LCIS, invasive lobular carcinoma (leads to unique pattern of metastasis - CSF, body cavities, ovaries)

18
Q

Cushingoid symptoms

A
Cataracts
Ulcers
Striae
Hypertension
Immunosuppression
Necrosis (femoral head)
Glycosuria
Obesity (incl. facial plethora, buffalo hump), Osteoporosis
Infections, Impaired wound healing
Diabetes
19
Q

Leiomyosarcoma histopathologic differentiation

A

Coagulative tumor cell necrosis (required for dx)

20
Q

PCOS classic presentation

A

Obese young woman with infertility, oligomenorrhea and hirsutism (might also have insulin resistance)

21
Q

2 most common causes of hypercalcemia

A

Hyperparathyroidism, tumor (hypercalcemia of malignancy)

22
Q

Primary hyperparathyroidism classic sx

A
"Stones, bones, groans and moans"
Stones: Ca ox in kidney
Bones: osteitis fibrosa cystica
Groans: GI things - pancreatitis, PUD, constipation/pain/N/V
Moans: depression, etc
23
Q

Calcium correction equation

A

measured calcium + 0.8(4.0 - measured albumin)

24
Q

Cardiac sequelae of hypercalcemia

A

Shortened QT interval

25
Q

How to determine high Alk phos etiology?

A

GGT - high in liver disease, normal if elevated alk phos is from bone

26
Q

Differentiate osteoporosis from osteomalacia

A

Osteoporosis (“issue with density, not quality”): caused by decr. estrogen and old age, no pain
Osteomalacia: inadequate bone mineralization (Ca++ and phosphate deficiency) most commonly caused by vitamin D deficiency; sx incl. bone pain (esp hips) and muscle weakness

27
Q

Endodermal sinus tumor characteristics

A

Yolk sac tumors – “SAC” mnemonic – Schiller-Duvall bodies (aka glomeruloid), AFP, Children (most common type)

28
Q

MEN 2A syndrome

A

Medullary thyroid cancer, pheochromocytoma, hyperparathyroidism

29
Q

MEN 2B (i.e. MEN III) syndrome

A

MEN 2A + Mucosal neuromas, Marfans-esque sx

30
Q

Define Waterhouse-Freidrichson syndrome

A

Adrenal gland failure (e.g. hypotension, shock) d/t bleeding, caused by Neisseria meningitidis infection