Pathology Buzz Words Flashcards
GNAS mutation
Pituitary adenoma
PAS+, POMC+
Corticotroph adenoma
Machine oil
Adamantinomatous Craniopharyngioma
Cyclin D1, MEN1 mutations
Sporadic Parathyroid Adenoma
MEN1, RET mutations
Familial parathyroid adenoma
PTHrP
Hypercalcemia of Malignancy
Chronic mucocutaneous candidiasis
Autoimmune cause of hypoparathyroidism
Primary adrenal insufficiency
Autoimmune cause of hypoparathyroidism
APS1
Autoimmune cause of hypoparathyroidism
Inherited hypoparathyroidism
GofF CASR, AD
Familial hypocalciuric hypercalcemia
CASR mutation, AD
Anti-microsomal Ab
Hashimoto thyroiditis
Anti-thyroid peroxidase Ab
Hashimoto thyroiditis
Anti-thyroglobulin Ab
Hashimoto thyroiditis
CTLA4, PTPN22 mutations
Hashimoto thyroiditis
Hurthle cell metaplasia
Hashimoto thyroiditis
Increased risk of Marginal Zone B-cell Lymphoma
Hashimoto thyroiditis
CTLA4, PTPN22, HLA-DR3 polymorphisms
Graves disease
Andes, Himalayas
Diffuse non-toxic goiter
RAS, PI3K, PTEN mutations
Follicular or Anaplastic thyroid carcinoma
BRAF mutation
Papillary thyroid carcinoma
Orphan Annie Eye nuclei
Papillary thyroid carcinoma
Ground glass appearance
Papillary thyroid carcinoma
Pseudo-inclusions
Papillary thyroid carcinoma
Neuroendocrine neoplasm in thyroid
Medullary thyroid carcinoma
RET mutatin
Medullary thyroid carcinoma
Stain + for calcitonin
Medullary thyroid carcinoma
Amyloid deposits in stroma
Medullary thyroid carcinoma
Carcinoembryonic Ag (CEA)
Sporadic medullary thyroid carcinoma
HLA-DR3, DR4, DR8
DM1
CTLA4, PTPN22, AIRE, Wasinsulin
DM1
Serum glucose of 600-1200
Hyperosmolar Hyperosmotic Syndrome
Serum glucose of 250-600
DKA
Kimmelstiel-wilson disease
Nodular glomerulosclerosis in DM pts
MEN1, PTEN, TSC2, ATRX syndrome, DAXX syndrome
Pancreatic neuroendocrine tumors
Pancreatic cells with amyloid deposits
Insulinoma
Stain + for PAS
Diffuse mesangial sclerosis
Ki-67 and p16
HSIL
PTEN, ARID1A mutations
Endometriosis
Serous carcinoma mutation
TP53
Mallignant Mixed Mullerian Tumor mutations
PTEN, TP53, PIK3CA
Leiomyoma mutation
MED12
Serous epithelial ovarian tumor mutation
BRCA1/2
Mucinous epithelial ovarian tumor mutation
KRAS
Endometrioid ovarian tumor mutation
PI3K/AKT
Dysgerminoma mutations
OCT-3/4, NANOG
Granulosa cell tumor mutation
FOXL2
Stertoli-Leydig cell tumor mutation
DICER1
Familial breast carcinoma genes
BRCA1/2, TP53, CHEK2
Breast cancer gene associated with increased risk of ovarian carcinoma
BRCA1
Breast cancer gene associated with increased risk of prostatic and pancreatic carcinoma
BRCA1/2
HER2+ mutation
TP53
ER+, HER2- mutations
BRCA2, PIK3CA
ER-, HER2- mutation
BRCA1
HOXB13 mutation
Phyllodes tumor