Pathology Buzz Words Flashcards

1
Q

GNAS mutation

A

Pituitary adenoma

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2
Q

PAS+, POMC+

A

Corticotroph adenoma

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3
Q

Machine oil

A

Adamantinomatous Craniopharyngioma

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4
Q

Cyclin D1, MEN1 mutations

A

Sporadic Parathyroid Adenoma

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5
Q

MEN1, RET mutations

A

Familial parathyroid adenoma

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6
Q

PTHrP

A

Hypercalcemia of Malignancy

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7
Q

Chronic mucocutaneous candidiasis

A

Autoimmune cause of hypoparathyroidism

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8
Q

Primary adrenal insufficiency

A

Autoimmune cause of hypoparathyroidism

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9
Q

APS1

A

Autoimmune cause of hypoparathyroidism

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10
Q

Inherited hypoparathyroidism

A

GofF CASR, AD

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11
Q

Familial hypocalciuric hypercalcemia

A

CASR mutation, AD

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12
Q

Anti-microsomal Ab

A

Hashimoto thyroiditis

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13
Q

Anti-thyroid peroxidase Ab

A

Hashimoto thyroiditis

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14
Q

Anti-thyroglobulin Ab

A

Hashimoto thyroiditis

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15
Q

CTLA4, PTPN22 mutations

A

Hashimoto thyroiditis

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16
Q

Hurthle cell metaplasia

A

Hashimoto thyroiditis

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17
Q

Increased risk of Marginal Zone B-cell Lymphoma

A

Hashimoto thyroiditis

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18
Q

CTLA4, PTPN22, HLA-DR3 polymorphisms

A

Graves disease

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19
Q

Andes, Himalayas

A

Diffuse non-toxic goiter

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20
Q

RAS, PI3K, PTEN mutations

A

Follicular or Anaplastic thyroid carcinoma

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21
Q

BRAF mutation

A

Papillary thyroid carcinoma

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22
Q

Orphan Annie Eye nuclei

A

Papillary thyroid carcinoma

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23
Q

Ground glass appearance

A

Papillary thyroid carcinoma

24
Q

Pseudo-inclusions

A

Papillary thyroid carcinoma

25
Q

Neuroendocrine neoplasm in thyroid

A

Medullary thyroid carcinoma

26
Q

RET mutatin

A

Medullary thyroid carcinoma

27
Q

Stain + for calcitonin

A

Medullary thyroid carcinoma

28
Q

Amyloid deposits in stroma

A

Medullary thyroid carcinoma

29
Q

Carcinoembryonic Ag (CEA)

A

Sporadic medullary thyroid carcinoma

30
Q

HLA-DR3, DR4, DR8

A

DM1

31
Q

CTLA4, PTPN22, AIRE, Wasinsulin

A

DM1

32
Q

Serum glucose of 600-1200

A

Hyperosmolar Hyperosmotic Syndrome

33
Q

Serum glucose of 250-600

A

DKA

34
Q

Kimmelstiel-wilson disease

A

Nodular glomerulosclerosis in DM pts

35
Q

MEN1, PTEN, TSC2, ATRX syndrome, DAXX syndrome

A

Pancreatic neuroendocrine tumors

36
Q

Pancreatic cells with amyloid deposits

A

Insulinoma

37
Q

Stain + for PAS

A

Diffuse mesangial sclerosis

38
Q

Ki-67 and p16

A

HSIL

39
Q

PTEN, ARID1A mutations

A

Endometriosis

40
Q

Serous carcinoma mutation

A

TP53

41
Q

Mallignant Mixed Mullerian Tumor mutations

A

PTEN, TP53, PIK3CA

42
Q

Leiomyoma mutation

A

MED12

43
Q

Serous epithelial ovarian tumor mutation

A

BRCA1/2

44
Q

Mucinous epithelial ovarian tumor mutation

A

KRAS

45
Q

Endometrioid ovarian tumor mutation

A

PI3K/AKT

46
Q

Dysgerminoma mutations

A

OCT-3/4, NANOG

47
Q

Granulosa cell tumor mutation

A

FOXL2

48
Q

Stertoli-Leydig cell tumor mutation

A

DICER1

49
Q

Familial breast carcinoma genes

A

BRCA1/2, TP53, CHEK2

50
Q

Breast cancer gene associated with increased risk of ovarian carcinoma

A

BRCA1

51
Q

Breast cancer gene associated with increased risk of prostatic and pancreatic carcinoma

A

BRCA1/2

52
Q

HER2+ mutation

A

TP53

53
Q

ER+, HER2- mutations

A

BRCA2, PIK3CA

54
Q

ER-, HER2- mutation

A

BRCA1

55
Q

HOXB13 mutation

A

Phyllodes tumor