A Case of Primary Hepatic Neuroendocrine Tumor and Literature Review

Author:

Wong Pak Chiu,She Wong Hoi,Khoo Ui Soon,Cheung Tan To

Abstract

We report an unusual presentation of primary hepatic neuroendocrine tumor which was initially misdiagnosed as intrahepatic cholangiocarcinoma. The diagnosis was only revealed after a major liver resection by histopathology. With adjuvant lanreotide injection, the patient survived for more than 16 months after the operation without tumor recurrence. Diagnosis of this rare tumor has been a major challenge and we emphasize the importance of a preoperative diagnosis. Surgical resection remains the mainstay for curative treatment, while peptide receptor radionuclide therapy is an emerging treatment option which has provided promising results.

Publisher

S. Karger AG

Subject

Oncology

Reference19 articles.

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3. Chan SC, Liu CL, Lo CM, Lam BK, Lee EW, Wong Y, et al. Estimating liver weight of adults by body weight and gender. World J Gastroenterol. 2006;12(14):2217–22.

4. Kunz PL, Reidy-Lagunes D, Anthony LB, Bertino EM, Brendtro K, Chan JA, et al. Consensus Guidelines for the Management and Treatment of Neuroendocrine Tumors, North American Neuroendocrine Tumor Society. Pancreas. 2013;42(4):557–77 .

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