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

Zentralbl Chir

Krankenhaus St. Joseph Stift, Klinik für Allgemein- und Viszeralchirurgie, Bremen, Deutschland.

Published: February 2012

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.

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Source
http://dx.doi.org/10.1055/s-0030-1262764DOI Listing

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