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阑尾黏液性囊腺瘤伴腹膜假黏液瘤和多囊性腹膜间皮瘤:一例报告

Appendiceal mucinous cystadenoma associated with pseudomyxoma peritonei and multicystic peritoneal mesothelioma: report of a case.

作者信息

Kusuyama T, Fujita M

机构信息

Department of Oncologic Surgery, Osaka University, Japan.

出版信息

Surg Today. 1995;25(8):745-9. doi: 10.1007/BF00311493.

Abstract

An extremely rare case of mucinous cystadenoma developing to pseudomyxoma peritonei together with multicystic peritoneal mesothelioma is herein reported. The patient was 25-year-old Japanese woman who underwent an appendectomy under the diagnosis of acute appendicitis because of right lower abdominal pain. The patient histopathologically demonstrated appendiceal mucocele with pseudomyxoma peritonei. She underwent a laparotomy in our unit following detailed examinations. Several cystic tumors measuring from 3 to 5 cm in diameter were found in the omentum, and thus omentectomy, partial cecectomy and left oophorectomy were all performed to resect the tumors. Immunostaining and electron microscopy showed the appendiceal lesion to be mucinous cystadenoma, while the peritoneal lesion was multicystic mesothelioma. To our knowledge, this is the first report in the world literature of this rare combination of diseases.

摘要

本文报告了一例极为罕见的黏液性囊腺瘤发展为腹膜假黏液瘤并伴有多囊性腹膜间皮瘤的病例。患者为一名25岁的日本女性,因右下腹痛在急性阑尾炎诊断下行阑尾切除术。患者组织病理学显示阑尾黏液囊肿伴腹膜假黏液瘤。经过详细检查后,她在我们科室接受了剖腹手术。在大网膜中发现了几个直径为3至5厘米的囊性肿瘤,因此进行了大网膜切除术、部分盲肠切除术和左侧卵巢切除术以切除肿瘤。免疫染色和电子显微镜检查显示阑尾病变为黏液性囊腺瘤,而腹膜病变为多囊性间皮瘤。据我们所知,这是世界文献中首次报道的这种罕见疾病组合。

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