Literature DB >> 205304

Clinically silent gross hypergastrinaemia from a multiple hormone-secreting pancreatic apudoma.

S N Joffe, E Elias, J F Rehfeld, J M Polak, S R Bloom, R B Welbourn.   

Abstract

A patient is described who had a malignant pancreatic islet cell apudoma secreting corticotrophin (ACTH) and melanocyte-stimulating hormone (MSH), both of which were clinically active, and very large quantities of immunoreactive gastrins, which were biologically active but clinically silent (normal gastric acid secretion and no peptic ulceration). The presence of parietal cell antibodies, with no increase in the plasma concentrations of hormones which can inhibit gastric acid secretion (secretin, GIP and VIP), suggests that many of the of the parietal cells may have been blocked by the autoantibodies.

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Year:  1978        PMID: 205304     DOI: 10.1002/bjs.1800650417

Source DB:  PubMed          Journal:  Br J Surg        ISSN: 0007-1323            Impact factor:   6.939


  3 in total

1.  Neuroendocrine tumors of the gut.

Authors:  P Durning; R B Galland; D M Nagorney; R B Welbourn
Journal:  World J Surg       Date:  1985-04       Impact factor: 3.352

2.  Clinical features and diagnosis of alimentary endocrine tumours.

Authors:  R B Welbourn
Journal:  J Clin Pathol Suppl (Assoc Clin Pathol)       Date:  1978

3.  Surgical management of the ectopic ACTH syndrome.

Authors:  C J Davies; G F Joplin; R B Welbourn
Journal:  Ann Surg       Date:  1982-09       Impact factor: 12.969

  3 in total

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