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阑尾原发性神经内分泌癌:病例报告及文献复习。

Primary neuroendocrine carcinoma of the appendix: a case report and review of the literature.

机构信息

Department of Gastroenterological Surgery, Shiroyama Hospital, Ota, Gunma, Japan.

出版信息

Anticancer Res. 2013 Jun;33(6):2635-8.

Abstract

AIM

We report on a rare case of appendiceal primary neuroendocrine carcinoma (NEC) and discuss three cases previously described.

CASE REPORT

A 58-year-old woman presented with acute abdominal pain and a low-grade fever. She was diagnosed with acute appendicitis and underwent laparoscopic appendectomy. Pathological examination of the resected specimen revealed NEC. Immunohistochemical analyses were positive for synaptophysin, chromogranin, and CD-56. The tumour was high grade and the Ki-67 index was >20%. Primary NEC of the appendix is extremely rare. To our knowledge, this is the first case report of an appendiceal NEC that meets the 2010 diagnostic criteria of the World Health Organization.

CONCLUSION

Due to its non-specific clinical presentation, NEC is often misdiagnosed as appendicitis; however, it can advance rapidly and carries a very poor prognosis, despite chemotherapy. In the future, a treatment protocol for immunohistochemical analyses should be established to improve the survival rate.

摘要

目的

我们报告一例罕见的阑尾原发性神经内分泌癌(NEC)病例,并讨论此前描述的三例病例。

病例报告

一名 58 岁女性因急性腹痛和低热就诊。她被诊断为急性阑尾炎,并接受了腹腔镜阑尾切除术。切除标本的病理检查显示为 NEC。免疫组织化学分析显示突触素、嗜铬粒蛋白和 CD-56 阳性。肿瘤分级较高,Ki-67 指数>20%。阑尾原发性 NEC 极为罕见。据我们所知,这是首例符合 2010 年世界卫生组织诊断标准的阑尾 NEC 病例报告。

结论

由于其非特异性临床表现,NEC 常被误诊为阑尾炎;然而,尽管进行了化疗,它仍可能迅速进展,预后极差。未来,应制定针对免疫组织化学分析的治疗方案,以提高生存率。

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