Primary hepatic carcinoid tumor: case report and literature review

被引：20

作者：

Camargo, Eden Sartor ^{[1
]}

Viveiros, Marcelo de Melo ^{[1
]}

Correa Neto, Isaac Jose Felippe ^{[1
]}

Robles, Laercio ^{[1
]}

Rezende, Marcelo Bruno ^{[1
]}

机构：

[1] Hosp Santa Marcelina, Sao Paulo, SP, Brazil

来源：

EINSTEIN-SAO PAULO | 2014年 / 12卷 / 04期

关键词：

Liver neoplasms; Neuroendocrine tumors/diagnosis; Carcinoid tumor; Case reports;

D O I：

10.1590/S1679-45082014RC2745

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Primary hepatic carcinoid tumors are extremely rare neoplasms derived from hormone-producing neuroendocrine cells. It is difficult to make their diagnosis before biopsy, surgical resection or necropsy. A recent publication described only 94 cases of these tumors. There is no sex predilection and apparently it has no association with cirrhosis or preexisting hepatic disease. The most effective treatment is hepatectomy, and resection is determined by size and location of the lesions.

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收藏

页码：505 / 508

页数：4

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