[Endocrine polyadenomatosis with carcinoid tumor]
- PMID: 15319
[Endocrine polyadenomatosis with carcinoid tumor]
Abstract
The authors review 26 cases of multiple endocrine tumours with presence of a carcinoid tumour. In 44% the carcinoid was localised to the bronchus, in 20% of cases to the small intestine or duodenum. In 76% of cases during multiple endocrine tumours, the carcinoid appeared in embryological derivatives of the anterior part of the intestine. No carcinoid syndrome was reported. The difficulty of histological distinction has led to the description of carcinoid islet cell tumours. These facts fit in with the APUD concept.
Similar articles
-
[Carcinoid of the bronchi and adenoma of the parathyroid: is it a fortuitous association or a multiple endocrine neoplasm?].Rev Clin Esp. 1989 Oct;185(5):268. Rev Clin Esp. 1989. PMID: 2575266 Spanish. No abstract available.
-
[Hyperinsulinism and polyendocrine adenomatosis].Folia Endocrinol. 1973 Oct;26(5):356-60. Folia Endocrinol. 1973. PMID: 4148796 Italian. No abstract available.
-
[Familial endocrine adenomatosis (author's transl)].Med Klin. 1979 Apr 6;74(14):520-3. Med Klin. 1979. PMID: 34783 German.
-
Duodenal carcinoid tumours, phaeochromocytoma and neurofibromatosis: islet cell tumour, phaeochromocytoma and the von Hippel-Lindau complex: two distinctive neuroendocrine syndromes.Q J Med. 1987 Sep;64(245):769-82. Q J Med. 1987. PMID: 2897130 Review.
-
Familial tumor endocrinopathies.Birth Defects Orig Artic Ser. 1971 May;7(6):55-65. Birth Defects Orig Artic Ser. 1971. PMID: 4155963 Review.