Neuroendokrinní karcinom pankreatu se syndromem hyperinzulinismu
[Neuroendocrine carcinoma of the pancreas with the hyperinsulinism syndrome]

. 1994 Oct 10 ; 133 (19) : 603-4.

Jazyk čeština Země Česko Médium print

Typ dokumentu kazuistiky, anglický abstrakt, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid07954674
Odkazy

PubMed 7954674

In a 26-year-old woman with symptoms of hyperinsulinism explorative laparotomy revealed a pancreatic tumour metastatizing into the liver. Intensive cytostatic therapy led to a temporary inhibition of hyperinsulinism, however, in the course of two years massive infiltration of the retroperitoneum, left adrenal, gastric wall, liver, mesentery and abdominal lymph nodes by a tumour occurred. On necroptic examination the tumour had characteristics of a neuroendocrine carcinoma with carcinoid features. Part of the tumour cells were argyrophil; reliable evidence of insulin production, which during the terminal stage of the disease played again a major part in the clinical picture, was made possible only by the use of a very sensitive Czech made antibody against C peptide.

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