[Poorly differentiated neuroendocrine small-cell carcinoma of the gallbladder].

Abstract:

BACKGROUND:Neuroendocrine tumours of the gastroenteropancreatic system (GEP-NETs) are rare, in particular those of the gallbladder. Due to the limited therapeutic options, surgical resection is favoured. CASE REPORT AND METHODS:Described below is the case of a 69-year-old male with a lymphogenically metastasising, poorly differentiated neuroendocrine carcinoma of the gallbladder who presented with unspecific abdominal pain. RESULTS AND CLINICAL COURSE:Following complete surgical resection of the tumour and the lymph node metastases he developed a recurrence 6  weeks post-operatively. The recurrence was treated with chemotherapy. Re-staging after three courses, however, showed further tumour progression. Prior to the start of a second-line treatment the patient died 13  weeks after surgery. CONCLUSIONS:This case demonstrates the complexity of this rare disease with diagnosis in advanced tumour stage and poor prognosis.

journal_name

Zentralbl Chir

authors

Benkel M,Brasch F,Neumann JD,Altendorf-Hofmann A,Sendt W

doi

10.1055/s-0030-1262764

subject

Has Abstract

pub_date

2012-02-01 00:00:00

pages

71-2

issue

1

eissn

0044-409X

issn

1438-9592

journal_volume

137

pub_type

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