Endocrine Flashcards

(36 cards)

1
Q

MCC of hyperpirtuitarism

A

functioning anterior pitiutary adenoma
1cm – can determine micro/macroadenoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

MC pituitary adenoma

A

Prolactin cell adenoma
2nd MC: Somatroph adenoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Origin of Craniopharygioma

A

Vestigial remnants of Rathke pouch
Hypothalamic suprasellar tumor
mass effect and hypopituitarism
bimodal age: 5-15, 65

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

hypermetabolic state caused by increase thyroid hormone level in the blood

A

Thyrotoxicosis

hyperthyroidism - thyrotoxicosis 2nd to thyroid gland hyperfunction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

MCC of primary hyperthyroidism

A

Graves disease
Type II HS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Posterior Pituitary Syndrome can be cause by this neoplasm

A

Small cell lung Ca

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

MCC of congenital hypothyroidism

A

Iodine deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

MCC of congenital hypothyroidism in Iodine sufficient areas

A

Autoimmune (Hashimoto)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

extensive fibrosis of the thyroid and contiguous neck structures

A

Riedel Thyroiditis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Painless thyroid enlargement
Autoantibodies against thyroglobulin and thyroid peroxidase
Hurtle cell changes
Lymphoplasmacytic infiltrates with germinal centers
+ fibrosis

A

Hashimoto thyroiditides

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Painless thyroid enlargement
Autoantibodies against thyroid peroxidase
family hx of autoimmunity
- fibrosis and hurtle changes

A

Subacute Lymphocytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

PainFUL thyroid enlargement
Antigen mediated immune damage to follicular cells
history of URTI prior to thyroiditis

A

Granulomatous thyroiditis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Most thyroid carcinoma arise from thyroid follicular epithelium, except

A

Medullary – Parafollicular C cells
assoc. with MEN2A, MEN2B
present with PAraneoplastic syndrome (VIP, ACTH) and high level of Calcitonin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

MC thyroid Ca

A

Papillary > Follicular
Favorable prognosis
+ Orphan annie nuclei
+ Psammoma Bodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Thyroid ca:
Pleomorphic giant cells
Spindle-shaped cells
IHC: Cytokeratin, PAX8

A

Anaplastic Thyroid Ca

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Most helpful thyroid differentiation marker in anaplastic Ca

17
Q

Thyroid Ca with Amyloid deposits

A

Medullary thyroid Ca
familial origin: C-cell hyperplasia
sheet of polygonal to spindle shaped cells in nests, trabeculae or follicules
IHC: Calcitonin

18
Q

most important susceptibility genes in T1DM

19
Q

TRIAD of DMT2

A

Genetic
Environmental - most important factor: Central/visceral obesity
Proinflammatory

20
Q

MCC of death in DM

A

Coronary heart disease
HM: accelerated atherosclerosis

21
Q

Insulin deficiency sufficient to develop KETOACIDOSIS

A

DKA
<7.25pH
+ ketones
visceral sx

22
Q

Insulin deficiency INSUFFICIENT to develop ketoacidosis

A

HHS
>7.30 pH
neurologic symptoms

23
Q

MC Pancreatic NET

A

Insulinomas
Hyperinsulinism
Whipple TRIAD
Amyloid deposition
loc: pancreas
benign

24
Q

Whipple TRIAD

A

Hypogylcemia <50mg/dl
Neuroglycopenic symptoms
Relief upon parenteral glucose administration

25
pancreatic islet cell tumor hypersecretion of gastric acid severe PUD
Zollinger-Ellison syndrome Seen in Gastrinoma -- malignant, located at Gastrinoma Triangle
26
Presentation of VIPoma
WDHA watery diarrhea Hypokalemia Achlorhydia
27
MCC overall of Cushing syndrome
Exogenous steroids/ Iatrogenic
28
MC endogenous cause of Cushing
ACTH secreting pituitary adenoma (Cushing Disease)
29
MCC of Primary hyperaldosteronism(Conn syndrome)
Bilateral idiopathic hyperaldosteronism neoplasm: Adenoma > Adrenocortical Carcinoma Secondary Hyperaldos - decreased renal perfusion
30
TRIAD of Pheochromcytoma
Diaphoresis Headaches Palpitations RULE OF 10s
31
Cytogenic origin of Pheochromocytoma
Chromaffin cells of medulla releases catecholamines Zellballen
32
Clusters of polygonal or spindle-shaped chromaffin or chief cells surrounded by sustentacular cells
Zell ballen
33
Rule of 10s
Extra -adrenal bilateral biological malignant not associated with hypertension 25% germline genetic mutations
34
Syndrome of MEN1
Wermer syndrome: Pituitary Parathyroid Pancreas
35
Syndrome of MEN2A mutation
Sipple sydrome mutation: RET Phechromocytoma, Medullary TCa, 2A: PArathyroid Neoplasm 2B: neuromas, ganglioneuromas, Marfanoid habitus
36
Syndrome of MEN2B
Wagemen-Froboese syndrome, Mucosal neuroma syndrome