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原发性腹膜后肿瘤:黏液囊腺癌。

Primary retroperitoneal tumor: mucinous cystoadenocarcinoma.

机构信息

Departamento de Cirugía General, Hospital Británico de Buenos Aires, Argentina. E-mail:

Departamento de Cirugía General, Hospital Británico de Buenos Aires, Argentina.

出版信息

Medicina (B Aires). 2024;84(4):750-755.

Abstract

Primary retroperitoneal mucinous cystadenocarcinomas (PRMCs) are extremely rare tumors with limited understanding of their pathogenesis and biological behavior. We describe a case of a 50-year-old female patient who underwent surgical treatment. The patient had a history of previous surgeries for mesenteric mucinous cystadenoma, without evidence of recurrence. During routine abdominal ultrasound a new tumor was found. An abdomen magnetic resonance imaging was done and confirmed the presence of a cystic lesion in the right iliac fossa. After discussion in multidisciplinary committee, surgical complete resection of the tumor, along with bilateral adnexectomy, was performed successfully. Histopathological examination revealed a mucinous adenocarcinoma adjacent to a mucinous cystadenoma. Immunohistochemical analysis supported the diagnosis of a primary retroperitoneal lesion. The patient had an uneventful recovery and has remained disease-free during the two-year postoperative follow-up. PRMCs are challenging to diagnose preoperatively due to nonspecific symptoms. Surgical excision is the mainstay of treatment. The long-term prognosis and optimal therapeutic strategies require further investigation.

摘要

原发性腹膜后黏液囊腺癌(PRMCs)是一种极为罕见的肿瘤,其发病机制和生物学行为了解有限。我们描述了一例 50 岁女性患者的病例,该患者接受了手术治疗。该患者曾因肠系膜黏液囊腺瘤接受过手术治疗,无复发证据。在常规腹部超声检查中发现了一个新的肿瘤。进行了腹部磁共振成像检查,证实右侧髂窝存在囊性病变。在多学科委员会讨论后,成功地进行了肿瘤的完全切除手术,同时进行了双侧附件切除术。组织病理学检查显示黏液性腺癌紧邻黏液囊腺瘤。免疫组织化学分析支持原发性腹膜后病变的诊断。患者术后恢复顺利,在两年的术后随访中无疾病复发。由于症状不典型,PRMCs 术前诊断具有挑战性。手术切除是主要的治疗方法。长期预后和最佳治疗策略需要进一步研究。

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