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侵袭性腹膜假黏液瘤:一例临床表现不寻常的病例报告。

Aggressive pseudomyxoma peritonei: a case report with an unusual clinical presentation.

作者信息

Touloumis Zisis, Galyfos George, Kavouras Nikolaos, Menis Michalis, Lavant Laurant

机构信息

Department of General Surgery, General Hospital of Chalkis, 48 Gazepi Street, Chalkis, 34100 Evia, Greece.

出版信息

Case Rep Oncol Med. 2013;2013:926963. doi: 10.1155/2013/926963. Epub 2013 Nov 13.

Abstract

Introduction. Pseudomyxoma peritonei (PMP) is an uncommon surgical entity. We report a case of aggressive disease with an unusual clinical presentation and we analyze current data on diagnosis and management of PMP. Case Presentation. A 71-year-old male patient presented with intermittent diarrhea and loss of appetite during the last two months, without any other classic symptoms of PMP. The clinical examination was misleading due to patient's obesity. The radiological evaluation revealed ascites of the abdomen and possible mucocele of the appendix, whereas the laboratory exams showed high values of specific tumour markers. The patient underwent an exploratory laparotomy for definite diagnosis. Biopsies and immunohistochemical examination confirmed the diagnosis of an aggressive and extended peritoneal mucinous carcinomatosis (PMCA). The patient was programmed for adjuvant systematic chemotherapy, which was not completed due to progression of the disease. Conclusions. Progressed PMP can present with unspecific symptoms that mislead diagnosis. Cytoreductive surgery in combination with systematic chemotherapy could be appropriate for aggressive PMCA, even with an unfavourable prognosis.

摘要

引言。腹膜假黏液瘤(PMP)是一种罕见的外科疾病。我们报告一例具有侵袭性且临床表现不寻常的病例,并分析当前关于PMP诊断和治疗的数据。病例报告。一名71岁男性患者在过去两个月出现间歇性腹泻和食欲不振,无PMP的任何其他典型症状。由于患者肥胖,临床检查产生误导。影像学评估显示腹部有腹水以及阑尾可能存在黏液囊肿,而实验室检查显示特定肿瘤标志物值升高。患者接受了剖腹探查术以明确诊断。活检和免疫组化检查确诊为侵袭性广泛性腹膜黏液性癌(PMCA)。该患者计划接受辅助全身化疗,但因疾病进展未完成化疗。结论。进展期PMP可能表现出非特异性症状,从而导致诊断失误。细胞减灭术联合全身化疗可能适用于侵袭性PMCA,即便预后不佳。

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