| Literature DB >> 26361431 |
Woo Young Shin1, Keon Young Lee1, Seung Ik Ahn1, Shin-Young Park1, Keun-Myoung Park1.
Abstract
Non-functioning pancreatic neuroendocrine tumors (NF-PNETs) are rare tumors that account for 2% of all pancreatic malignancy. About 60% of NF-PNETs present distant metastases and usually hepatic metastases. However, cutaneous metastases are very rare. Herein, we report our experience with a 60-year-old male who visited our outpatient clinic with a mass on his left hip. An abdominal computerized tomography scan demonstrated not only a left hip mass and an enlarged left inguinal lymph node, but also a huge heterogeneous enhancing mass on the pancreas. Initially, we removed the metastatic lesions, which was a small cell neuroendocrine carcinoma with 50% of the Ki-67 index in the histopathological report. After 3 wk, we performed a total pancreatectomy and a total gastrectomy. Four weeks after the 1(st) operation, we detected a recurrence at the operative bed on his left hip, and subsequently removed the recurring mass. The patient was receiving chemotherapy based on etoposide and cisplatin treatment.Entities:
Keywords: Neoplasm metastasis; Neuroendocrine tumor; Pancreas; Pancreatectomy; Skin neoplasm
Mesh:
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Year: 2015 PMID: 26361431 PMCID: PMC4562968 DOI: 10.3748/wjg.v21.i33.9822
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742