Literature DB >> 21365540

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

M Benkel1, F Brasch, J D Neumann, A Altendorf-Hofmann, W Sendt.   

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. © Georg Thieme Verlag KG Stuttgart ˙ New York.

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Year:  2011        PMID: 21365540     DOI: 10.1055/s-0030-1262764

Source DB:  PubMed          Journal:  Zentralbl Chir        ISSN: 0044-409X            Impact factor:   0.942


  2 in total

Review 1.  Surgical treatment of liver metastases in patients with neuroendocrine tumors.

Authors:  Ahmad Saeed; Joseph F Buell; Emad Kandil
Journal:  Ann Transl Med       Date:  2013-04

Review 2.  Surgical approaches for liver metastases in carcinoid tumors.

Authors:  Emad Kandil; Ahmad Saeed; Joseph Buell
Journal:  Gland Surg       Date:  2015-10
  2 in total

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