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thyroid
medullary carcinoma
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Clinical
5% of thyroid cancer
can be hereditary
RET proto-oncogene
familial medullary thyroid carcinoma
MEN II
medullary carcinoma
pheochromocytoma
parathyroid adenoma
MEN IIB also has:
marfanoid habitus
mucosal and GI neurofibromatosis
elevated calcitonin
elevated CEA in late disease
half have positive nodes
Histology
architecture
solid
lobular
trabecular
insular
sheetlike
amyloid in 80% of cases
giant cell reaction
cytology
round
polygonal
spindle
mixed
arises from C cells
cytoplasmic grooves, pseudoinclusions
nuclear
salt and pepper chromatin
binucleate
variants
follicular
trabecular
papillary
paraganglioma-like
amphicrine
small cell
giant cell
clear cell
encapsulated
oncocytic
melanotic
squamous
Stains
calcitonin+
chromogranin, synaptophysin+
CEA+
congo red stains amyloid
thyroglobulin negative
Ddx
C cell hyperplasia
reactive C cell hyperplasia
nodular C cell hyperplasia
both lack fibrosis
other thyroid carcinomas are calcitonin negative