ENDO Flashcards

1
Q

Prolactinoma

Comp?

A

COMP:

- Impingement of optic chiasm -> Bitemporal Hemianopia

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2
Q

NONFUNCTIONAL Pituitary Adenomas

Potential Pres (3)?

A

POTENTIAL PRES:

  • Hypopituitarism (due to compression of normal pituitary tis)
  • Bitemporal Hemianopsia (due to compression of optic chiasm)
  • Headache
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3
Q

Pituitary Adenomas

2 Variations, Comp?

A
  • Functional: Hormone-producing
  • Nonfunctional: Silent. Often produce mass effect.

COMP:
- Islet Cell tumor

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4
Q

Empty Sella Sx

Def’n, Mech (3 steps), Pres (Epi), Imaging?

A

Congenital defect of Sella Turcica.

MECH:
Defective Sella Turcica ->
Herniation of arachnoid + CSF into it ->
Compression / destruction / atrophy of Pituitary.

PRES: Obese Women

IMAGING: Pituitary ABSENT on imaging

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5
Q

Hypopituitarism

Causes (5)?

A

CAUSES:

    • Pituitary Adenoma / Craniopharyngioma
  • Empty Sella Sx
  • Sheehan Sx
  • Brain injury / hem
  • Radiation
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5
Q

Sheehan’s Sx

Def’n, Mech (2 steps), Pres (3)?

A

Postpartum Bleeding -> Hem / Ischemic INFARCT of Pituitary.

MECH:

  • Pituitary doubles in size during pregnancy, however its bl supply does NOT increase significantly.
  • Bl loss during labor -> Pituitary infarct

PRES:

  • Cold Intolerance + Fatigue
  • Absent menses
  • Failure to lactate
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6
Q

Diabetes Insipidus

Mech, Assoc,
Pres (2), Labs (Bl, Urine)?

A

MECH = Lack of ADH (Central) / Lack of response to ADH (Nephrogenic).
Loss of Free H2O

ASSOC:
- Hand-Schuller Christian Dz

PRES:

  • Intense thirst + Polyuria
  • Inability to concentrate urine

LABS:

  • HIGH Serum Osm > 290
  • LOW Urine Osm / Specific Gravity
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7
Q

Central DI

Mech, Causes (4), RX?

A

MECH = LACK of ADH.

CAUSES:

  • Surgery
  • Trauma
  • Histiocytosis X
  • Pituitary tumor

RX: Intranasal Desmopressin (ADH analog)

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8
Q

SIADH

Mech (3 steps), Causes (4), Pres / Labs, RX (2)?

A

MECH:
Excessive ADH secretion ->
Retention of Free H2O ->
↓Aldosterone (body’s response to maintain near-normal volume status).

CAUSES:

  • Small Cell Carcinoma of Lung (ectopic ADH)
  • Pulmonary dz
  • CNS disorders / trauma
  • Cyclophosphamide

PRES: Excessive water retention

  • Hyponatremia (due to↓Aldosterone)
    - > Low Serum Osm
    - > Neuronal swelling + Cerebral Edema

RX:

  • Water restriction
  • Demeclocycline
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8
Q

Nephrogenic DI

Mech, Causes (4), RX (3)?

A

MECH = Lack of renal RESPONSE to ADH.

CAUSES:

  • Hereditary
  • Hypercalcemia
  • Demeclocycline use (ADH antagonist)
  • Lithium use

RX:

  • Amiloride
  • Hydrochlorothiazide
  • Indomethacin
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9
Q

Neuroblastoma

Location, RF (Genetic), Pres, Urine?

A

Can occur anywhere along sympathetic chain.

RF:
- Overexpression of N-myc oncogene (assoc with rapid tumor prog)

PRES: LESS likely to devel Htn compared to Pheochromocytoma

URINE:
-↑HVA (b/d product of dopamine)

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10
Q

Pheochromocytoma

Seen In (4), Pres?

A

SEEN IN:

  • MEN 2
  • All Neurocutaneous Disorders EXCEPT Tuberous Sclerosis*
  • Sturge-Weber Sx
  • Neurofibromatosis Type 1
  • Von Hippel-Lindau Dz

PRES: Symptoms occur in spells- relapse and remit. Are result of catecholamine secretion by tumors.

  • Episodic Htn
  • Tachycardia + Palpitations
  • Sweating
  • Headache
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11
Q

21-hydroxylase Deficiency

Pres (2)?

A

PRES:

  • CONGENITAL adrenal hyperplasia
  • Hypotension
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12
Q

1ry Hyperaldosteronism

Pres (2), Labs (3)?

A

PRES: Uni- or bilateral

  • Htn (↑bl Na + H20 ->↑plasma volume)
  • Metabolic Alkalosis (↑H + K secretion)

LABS:

  • Renin↓(high B.P downregulates renin)
  • Aldosterone↑
  • Na + H2O↑
  • H + K ↓
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13
Q

2ry Hyperaldosteronism

Causes (3), Labs (2)?

A

CAUSES:

  • CHF
  • Renovascular Htn (Nephrotic Sx, Renal art Stenosis, Chronic RF)
  • Cirrhosis

LABS:

  • Renin↑
  • Aldosterone↑
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14
Q

Conn Sx

Pres (2)?

A

PRES:

  • Htn
  • Metabolic Alkalosis (-> Hypokalemia)
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15
Q

Cushing’s Sx

Pres (7), Labs (2), DX (2)?

A

PRES:
- “Moon facies, Truncal obesity, Buffalo hump”
(↑glucose -> ↑insulin -> ↑fat storage)
- Weight gain
- Htn
- Amenorrhea
- Immune suppression
- Skin thinning + striae (impaired collagen syn)
- Osteoporosis, thin extremities + muscle weakness (Cortisol b/d muscle for gluconeogenesis)

LABS:

  • Hyperglycemia
  • Eosinopenia

DX:

  • 24h Urine:↑Cortisol levels
  • Dexamethasone Suppression Test
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16
Q

Addison Disease

Mech, Causes (3), Pres (4: CLUE + 3), Labs (4)?

A

MECH:↑ACTH + MSH production

CAUSES:

  • Autoimmune dz MC in West
  • TB MC in developing world
  • Metastasis (from lung)

PRES: Deficiency of Aldosterone + Cortisol

  • Hypotension (hyponatremic vol contraction)
  • Acidosis (Aldosterone def ->↑H)
  • Fatigue, Vomiting + Diarrhea
  • “Skin hyperpigmentation” (Cortisol def ->↑ACTH -> ↑MSH)

LABS:

  • Aldosterone↓
  • Cortisol↓
  • Na↓
  • H + K↑
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17
Q

Waterhouse-Friderichsen Sx

Causes / Assoc (3)?

A

CAUSES / ASSOC:

  • Neisseria meningitidis septicemia (young children)
  • Endotoxic Shock and Hypotension
  • DIC
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18
Q

Hyperthyroidism

Mech (2), Causes (2)?

A

MECH:

  • ↑BMR (due to↑syn of Na/K ATPase)
  • ↑SNS activity (due to↑expression of b1-receptors)

CAUSES:

  • Struma Ovarii
  • Choriocarcinoma (male + female)
19
Q

Graves Dz

Pres (Epi + Envir + 3), Labs, Histo (2), Comp?

A

PRES: MC in women 20-40

  • Times of stress (ie childbirth)
  • Exophthalmos, Proptosis, Eyelid retraction / Sclera visible
  • Pretibial Myxedema
  • Diffuse Goiter (thyroid hyperplasia + hypertrophy)

LABS:
- ALP↑(due to↑bone turnover)

HISTO:

  • Irregular thyroid follicles
  • Chronic infl

COMP:
- Thyroid Storm

20
Q

Thyroid Storm

Def’n, Pres (4)?

A

Stress-induced CATECHOLAMINE surge leading to death by arrhythmia.

PRES:

  • Arrhythmia
  • Hyperthermia
  • Hypovolemic Shock
  • Vomiting
21
Q

Multinodular Goiter

Mech (4 steps), Causes (2), Comp?

  • Goiters usually non-toxic
  • Hot nodules rarely malignant
A
MECH:
Mutation in TSH receptor ->
Patches of HYPERfunctioning follicular cells working INDEP of TSH ->
↑release of T3 + T4 ->
Hyperthyroidism.

CAUSES:

  • Iodine def
  • Mutation in TSH receptor

COMP:
- Jod-Basedow Phenomenon: THYROTOXICOSIS if patient with Iodine-def-goiter made Iodine-replete.

23
Q

Hashimoto’s Thyroiditis

HLA, Ab, Pres (2), Clinical Course, Micro Findings (2), Comp?

A

HLA-DR5.

Antimicrosomal Antithyroglobulin antibodies.

PRES:

  • Moderately enlarged NONTENDER thyroid
  • Myxedema

HYPERthyroidism early in course (thyrotoxicosis during follicular rupture) -> Progression to HYPOthyroidism.

FINDINGS:

  • Hurthle cells
  • Chronic infl / lymphocytic infiltrate with germinal centers

COMP:
- NHL

24
Cretinism Def'n, Pres (4)?
Hypothyroidism in neonates and infants. PRES: - Pale, puffy-face, coarse facial features + enlarged tongue - Pot-belly with protruding umbilicus / umbilical hernia - Short stature + skeletal abnormalities - MR * Thyroid hormone req for CNS + skeletal devel *
24
Sporadic Cretinism Causes (3)?
CAUSES: - Devel failure in thyroid formation (ie from maternal hypothyroidism in early pregnancy) - 'Dyshormonogenetic Goiter' (congenital defect in T4 production) - Thyroid agenesis
25
Subacute (de Quervain's) Thyroiditis Def'n, Pres (General + 1), Clinical Course, Labs?
Granulomatous thyroiditis. PRES: Self-limited hypothyroidism following flu / virus. - Tender thyroid + jaw pain Can be HYPERthyroid early in course. LABS: - ESR ↑
26
Riedel's Thyroiditis Def'n, Pres (2), Comp?
Chronic infl + extensive fibrosis of thyroid (ie thyroid replaced by fibrous tis). PRES: - Painless goiter - Fixed, hard ("rock-like") thyroid COMP: - Fibrosis may extend to nearby structures (ie airways)
27
Thyroid Carcinoma (Papillary Carcinoma) RF, Pres (2 General), Micro Findings (3), DX (2), Mets, Prognosis?
RF: - Childhood irradiation PRES: - MC as solitary and distinct nodule - MC benign FINDINGS: Enlarged thyroid cells with: - "Ground-glass" / "Orphan Annie eyes" nuclei - Nuclear grooves - Psammoma bodies DX: - I Radioactive Uptake studies (↑uptake = hot nodules,↓uptake = cold nodules) - Biopsy by Fine Needle Aspiration METS: -> Cervical lymph nodes PROG = Excellent!
28
Anaplastic / Undifferentiated Thyroid Carcinoma Pres (Epi + 2), Mets, Prognosis?
PRES: Older patients - Dysphagia - Resp compromise METS: Often invades local structures PROG = Very poor!
29
Thyroid Lymphoma Assoc?
ASSOC: | - Hashimoto's Thyroiditis
30
Medullary Thyroid Carcinoma Def'n, Assoc, Pres, Micro Finding, Prevention?
Malignant prolif of parafollicular C cells. ASSOC: (Familial cases) - Men 2 (mutations in RET oncogene) PRES: Calcitonin production (-> Hypocalcemia) FINDING: - Amyloid sheets (Calcitonin deposits) PREV: - Detection of RET oncogene -> Prophylactic Thyroidectomy
31
Hypoparathyroidism Causes (2), Pres (2), Phys Findings (2 Signs)?
CAUSES: * - Accidental excision during thyroidectomy - Autoimmune destruction / DiGeorge Sx PRES: *Related to HYPOcalcemia* - Numbness + Tingling - Tetany PHYS FINDINGS: - Chvostek's sign (facial muscles) - Trousseau's sign (carpal)
32
Pseudohypoparathyroidism = Albright's Hereditary Osteodystrophy Def'n, Inher, Pres (2)?
Kidney UNRESPONSIVENESS to PTH. AD. PRES: *HYPOcalcemia* - Short stature - Shortened 4th / 5th digits
33
Hyperparathyroidism #1- CAUSES 1ry (3), 2ry, 3ry?
CAUSES: - 1ry: Hyperplasia, Adenomas, Carcinoma - 2ry: HYPOcalcemia of Chronic Kidney Disease / RF - 3ry: Chronic Kidney Disease / RF
34
Hyperparathyroidism #2- PRES 1ry ("Stones (2 Renal), Bones and Groans"), 2ry / 3ry (Renal Osteodystrophy MECH (8 steps))?
PRES: 1ry: - "Stones": Nephrolithiasis (Ca Oxalate stones / Hypercalciuria) + Nephrocalcinosis (metastatic calc of renal tubules) - "Bone (pain)": Osteitis Fibrosa Cystica (Bone resorption -> fibrosis and cystic spaces) - "Groans (constipation)": Peptic Ulcer Dz 2ry / 3ry: MECH: Renal dz / insufficiency -> ↓P excretion ->↑serum P binds free Ca ->↓free Ca -> Stim Parathyroids -> ↑PTH -> Bone resorption -> Bone lesions.
36
Hyperparathyroidism #3- LABS / URINE 1ry (incl Urine), 2ry, 3ry?
LABS / URINE: 1ry: - Bl: Ca↑, P↓, ALP↑ - Urine: Ca↑, cAMP ↑ 2ry: - Bl: Ca↓, P↑, ALP↑ 3ry: - Bl: Ca↑ *** PTH VERY ↑***
37
Parathyroid Hyperplasia (-> 1ry Hyperparathyroidism) Comp?
COMP: | - Islet Cell tumor
38
Chvostek Sign Pres, Significance?
Facial muscle spasm upon tapping. Significance = Hypocalcemia.
39
Islet Cell Tumor Assoc (3)?
ASSOC: Often a component of: - Pituitary Adenomas - Parathyroid Hyperplasia - Men I
40
Insulinoma Pres, Labs (3)?
PRES: - Episodic Hypoglycemia *with mental status changes*, relieved by admin of glucose LABS: - Glucose
41
Gastrinoma Def'n / 2 Locations, Assoc (Potential), Pres?
Gastrin-secreting tumor of Pancreas or Duodenum. ASSOC (Potential): - Men I PRES = Zollinger-Ellison Sx
42
Somatostatinoma (Somatostatin-secreting tumor) Pres, Labs?
PRES = Cholelithiasis + Steatorrhea (due to inhib of CCK) LABS: - HYPOchlorhydria (due to inhib of Gastrin / production of gastric acid)
43
VIPoma (VIP-secreting tumor) Mech, Pres, Labs (2)?
MECH:↑VIP ->↑intestinal secretions -> smooth muscle RELAXATION in GI tract PRES = Watery Diarrhea LABS: - HYPOchlorhydria (due to inhib of Gastrin / production of gastric acid) - HYPOkalemia
44
MEN 1 (Wermer's Sx) Pres ("3 Ps" Tumors + 2)?
PRES: - Pituitary tumors (GH or Prolactin) - Parathyroid tumors - Pancreatic tumors (ENDOCRINE: Z-E Sx, Insulinomas, VIPomas) - Stomach ulcers - Kidney stones
44
MEN Sx Inher, Genetics?
AD. ret gene (MEN 2).
46
MEN 2A (Sipple's Sx) Pres (2)?
PRES: - Thyroid AND Parathyroid tumors - Pheochromocytoma
47
MEN 2B Pres (3)?
PRES: - Medullary Thyroid Carcinoma (secretes Calcitonin) - Pheochromocytoma - Oral/Intestinal Ganglioneuromatosis
48
McCune-Albright Sx Path / Genetics, Pres (4: General + 3)?
G-protein signaling mutation. | ``` PRES: - Endocrine abnormalities - - Precocious Puberty - Cafe-au-Lait spots - Polyostotic fibrous dysplasia ```