Dr Md Manir Hossain Khan, Associate Professor, Department of Surgery, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh; E-mail:
Mymensingh Med J. 2021 Jan;30(1):224-227.
Lymphangioma is a rare, benign tumour occurring due to congenital malformation of the lymphatic channels. It occurs due to obstruction in the lymphatic channel and results in lymphangiectasia. The tumour is most commonly encountered in the head and neck regions and almost 90% are in the children below the age of 2 years. Retroperitoneal Lymphangioma in an adult is a rare clinical condition. We have presented a 41 year old female with retroperitoneal lymphangioma who came to Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh on 10 October 2017 with the non-specific complains of upper abdominal discomfort, occasional nausea, vomiting and aorexia for the last 1.5 years. She was managed surgically by exploratory laparotomy followed by de-roofing of the cyst. Histopathological examination of the cyst wall was consistent with lymphangioma.
淋巴管瘤是一种罕见的良性肿瘤,由于淋巴管的先天性畸形而发生。它是由于淋巴管阻塞而导致淋巴管扩张。这种肿瘤最常见于头颈部,几乎 90%发生在 2 岁以下的儿童中。成人腹膜后淋巴管瘤是一种罕见的临床病症。我们报告了一名 41 岁女性腹膜后淋巴管瘤患者,她于 2017 年 10 月 10 日来到孟加拉国达卡的 Bangabandhu Sheikh Mujib 医学大学(BSMMU),以上腹部不适、偶尔恶心、呕吐和厌食为主要症状,持续了 1.5 年。她接受了剖腹探查术,然后进行了囊肿去顶术。囊肿壁的组织病理学检查与淋巴管瘤一致。