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一名63岁女性肠系膜囊性淋巴管瘤误诊为卵巢囊肿:病例报告及文献复习

Mesenteric cystic lymphangioma misdiagnosed as ovarian cyst in a 63-year-old female: A case report and review of literature.

作者信息

Mahfoud Hounaida, Flissate Farah, Tligui Samia, Benammi Sarah, Etber Amina, Baidada Aziz

机构信息

Gynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat, Morocco.

Gynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat, Morocco.

出版信息

Int J Surg Case Rep. 2024 Jul;120:109846. doi: 10.1016/j.ijscr.2024.109846. Epub 2024 Jun 1.

Abstract

INTRODUCTION

Cystic lymphangioma is rare benign tumor that results from a lymphatic system malformation. The mesenteric location is even more uncommon.

CASE REPORT

We report the case of a menopausal 63-year-old woman who presented with a persistent painful well-defined mass of the pelvis. On ultrasound and computed tomography, the mass appeared as thick-walled unilocular homogenous cyst in favor of an ovarian cystadenoma. During laparotomy, the misdiagnosis was confirmed as the tumor was found to be embedded in the mesentery of the ileum. Subsequent histopathological examination confirmed the benign cystic lymphangioma diagnosis.

DISCUSSION

Mesenteric cystic lymphangioma is rare peritoneal tumor of the adult. Clinically, it often masquerades as other abdominopelvic masses like ovarian cysts. Differential diagnosis is often challenging because of the overlapping clinical abdominal presentation and radiological features. Histopathological is the gold standard in diagnosing mesenteric cystic lymphangioma. Surgery is the mainstay treatment, and the recurrence rate is low if negative surgical margins are achieved.

CONCLUSION

Mesenteric cystic lymphangioma often mimics more frequent and potentially malignant lesions. It is essential for surgeons to remain vigilant for the possibility of this diagnosis when evaluating abdominopelvic cystic masses.

摘要

引言

囊性淋巴管瘤是一种由淋巴系统畸形引起的罕见良性肿瘤。肠系膜部位更为少见。

病例报告

我们报告一例63岁绝经后女性病例,该患者盆腔出现一个持续疼痛、边界清晰的肿块。超声和计算机断层扫描显示,该肿块表现为厚壁单房均匀囊肿,提示为卵巢囊腺瘤。剖腹手术时,发现肿瘤嵌入回肠系膜,误诊得到证实。随后的组织病理学检查确诊为良性囊性淋巴管瘤。

讨论

肠系膜囊性淋巴管瘤是成人罕见的腹膜肿瘤。临床上,它常伪装成其他腹盆腔肿块,如卵巢囊肿。由于临床腹部表现和影像学特征重叠,鉴别诊断往往具有挑战性。组织病理学是诊断肠系膜囊性淋巴管瘤的金标准。手术是主要治疗方法,如果手术切缘阴性,复发率较低。

结论

肠系膜囊性淋巴管瘤常模仿更常见且可能为恶性的病变。外科医生在评估腹盆腔囊性肿块时,必须警惕这种诊断的可能性。

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