Perforated High-Grade Mixed Neuroendocrine Nonneuroendocrine Neoplasm of Cecum: Unusual Presentation of Rare Disease.

IF 0.8 Q4 GASTROENTEROLOGY & HEPATOLOGY Gastrointestinal Tumors Pub Date : 2021-06-01 Epub Date: 2021-04-20 DOI:10.1159/000512237
Gunasekaran Gopalakrishnan, Bheemanathi Hanuman Srinivas, Biju Pottakkat, Senthil Gnanasekaran, Raja Kalayarasan
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引用次数: 2

Abstract

Mixed neuroendocrine nonneuroendocrine neoplasms (MiNENs) are rare neoplasms of the gastrointestinal tract, where the neuroendocrine as well as the nonneuroendocrine components each comprise at least 30% of the tumor. Of all cases of colorectal malignancies, MiNENs constitute around 3-9.6%, with only a few cases reported to be arising in the cecum. Since majority present with nonspecific clinical and radiological findings, its diagnosis preoperatively is almost impossible and these are usually diagnosed after histopathological examination of the resected specimen. Owing to the rarity of these tumors as well as lack of complete molecular characterization, optimal treatment remains unestablished. We, here, report a rare case of MiNENs of the cecum infiltrating the right psoas muscle and presenting with perforation for which right hemicolectomy and en bloc excision of the involved psoas muscle was done followed by adjuvant chemotherapy.

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盲肠穿孔高级别混合神经内分泌非神经内分泌肿瘤:罕见疾病的不寻常表现。
混合性神经内分泌非神经内分泌肿瘤(MiNENs)是一种罕见的胃肠道肿瘤,其中神经内分泌和非神经内分泌成分各占肿瘤的30%以上。在所有结直肠恶性肿瘤病例中,MiNENs约占3-9.6%,据报道只有少数病例发生在盲肠。由于大多数表现为非特异性临床和影像学表现,术前诊断几乎是不可能的,这些通常是在切除标本的组织病理学检查后诊断。由于这些肿瘤的罕见性以及缺乏完整的分子特征,最佳治疗仍未确定。在此,我们报告一例罕见的盲肠MiNENs浸润右腰肌并出现穿孔的病例,在此病例中,我们对受累的腰肌进行了右半结肠切除术和整体切除,并进行了辅助化疗。
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来源期刊
Gastrointestinal Tumors
Gastrointestinal Tumors GASTROENTEROLOGY & HEPATOLOGY-
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审稿时长
17 weeks
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