腹膜假肌瘤并发阑尾粘液瘤

Z. Amzal, M. Kadiri, M. Borahma, F. Chabib, N. Lagdali, C. Berhili, I. Benelbarhdadi, F. Ajana
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引用次数: 0

摘要

阑尾粘液瘤(AM)或阑尾粘液性肿瘤是一种罕见但具有潜在危险性的疾病。在后者中,粘液瘤的自发性或先天性破裂可导致粘液性腹腔腹水,这种综合征被称为假性腹膜肌瘤。我们报告的病例是一名 76 岁的女性患者,临床检查时报告右髂窝疼痛并伴有 RIF 触痛,腹部 CT 扫描显示阑尾粘液瘤伴有少量腹腔积液,怀疑粘液瘤破裂,与腹膜假性肌瘤有关。患者接受了阑尾切除术,并进行了腹腔灌洗,吸出了所有粘液。解剖病理分析证实了阑尾粘液瘤(一种低级别阑尾粘液瘤)的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Appendicular Mucocele Complicated by Peritoneal Pseudomyxoma
Appendiceal mucocele (AM) or Appendiceal mucinous neoplasms is a rare but potentially dangerous condition. In the latter, a spontaneous or iatrogenic rupture of the mucocele can lead to mucinous intraperitoneal ascites, a syndrome known as pseudomyxoma peritonei. We present the case of a 76-year-old female patient who reported right iliac fossa pain with RIF tenderness on clinical examination, and underwent an abdominal CT scan showing an appendiceal mucocele associated with a small peritoneal effusion suspecting a ruptured mucocele, related to peritoneal pseudomyxoma. The patient underwent appendectomy with peritoneal lavage and aspiration of all mucin found. Anatomopathological analysis confirmed the diagnosis of appendiceal mucocele (a low-grade appendiceal mucinous neoplasm).
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