A case of multiple endocrine adenomatosis (Type 1) with nesidioblastosis, terminating with an exocrine pancreatic carcinoma.

Abstract:

:We describe a patient with multiple endocrine adenomatosis Type I, characterized by pituitary-dependent Cushing's Syndrome, marked hyperprolactinaemia, primary hyperparathyroidism and hyperinsulinism leading to hypoglycaemia. The patient subsequently developed an exocrine pancreatic carcinoma at the age of 32 years from which she died. An additional finding was the demonstration by immunocytochemistry of nesidioblastosis in the pancreas.

journal_name

Clin Endocrinol (Oxf)

journal_title

Clinical endocrinology

authors

Oliver MH,Drury PL,Van't Hoff W

doi

10.1111/j.1365-2265.1983.tb02879.x

subject

Has Abstract

pub_date

1983-05-01 00:00:00

pages

495-403

issue

5

eissn

0300-0664

issn

1365-2265

journal_volume

18

pub_type

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