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一例原发性不明的神经内分泌肿瘤,其根据肿瘤分级进展对治疗产生反应。

A Neuroendocrine Tumor of Unknown Primary Origin that Responded to Treatment Based on Tumor Grade Progression.

作者信息

Hamano Yukako, Moriwaki Toshikazu, To Keii, Watahiki Takahisa, Yamada Takeshi, Sakashita Shingo, Hyodo Ichinosuke

机构信息

Department of Gastroenterology, Faculty of Medicine, University of Tsukuba, Japan.

Department of Pathology, Faculty of Medicine, University of Tsukuba, Japan.

出版信息

Intern Med. 2019 Apr 15;58(8):1087-1091. doi: 10.2169/internalmedicine.1809-18. Epub 2018 Dec 18.

DOI:10.2169/internalmedicine.1809-18
PMID:30568142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6522411/
Abstract

The standard chemotherapies for neuroendocrine tumors (NETs) are somatostatin analog (SSA) and targeted-agents for NET G1/G2 and platinum-based chemotherapy for neuroendocrine carcinoma (NEC), classified according to the WHO criteria of 2010. We report a case of NET, in which tumors were successfully treated with platinum-containing chemotherapy after remarkable progression with SSA. A 46-year-old man with multiple lymph nodes and liver metastases of unknown primary origin was diagnosed with NET G2 based on the examination of a biopsy specimen. His tumors were stable with SSA for a year, but rapidly became enlarged. A second biopsy revealed NEC. He received cisplatin plus etoposide, and his tumors showed a marked reduction in size.

摘要

根据2010年世界卫生组织标准,神经内分泌肿瘤(NETs)的标准化疗方案是:NET G1/G2采用生长抑素类似物(SSA)和靶向药物,神经内分泌癌(NEC)采用铂类化疗。我们报告一例NET病例,该患者在使用SSA治疗显著进展后,采用含铂化疗成功治疗。一名46岁男性,多发淋巴结及肝脏转移,原发灶不明,经活检标本检查诊断为NET G2。其肿瘤用SSA治疗一年病情稳定,但随后迅速增大。再次活检显示为NEC。他接受了顺铂加依托泊苷治疗,肿瘤大小显著缩小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/7a109c9d5cde/1349-7235-58-1087-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/8da958800887/1349-7235-58-1087-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/051c970b8e29/1349-7235-58-1087-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/7a109c9d5cde/1349-7235-58-1087-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/8da958800887/1349-7235-58-1087-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/051c970b8e29/1349-7235-58-1087-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/653f/6522411/7a109c9d5cde/1349-7235-58-1087-g003.jpg

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Well-Differentiated Neuroendocrine Tumors with a Morphologically Apparent High-Grade Component: A Pathway Distinct from Poorly Differentiated Neuroendocrine Carcinomas.具有形态学上明显高级别成分的高分化神经内分泌肿瘤:一条与低分化神经内分泌癌不同的途径。
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Characteristics and treatment of patients with G3 gastroenteropancreatic neuroendocrine neoplasms.G3 胃肠胰神经内分泌肿瘤患者的特征与治疗
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