肺外淋巴管平滑肌瘤表现为肠系膜囊性肿块

Young Jin Jun, Se Min Jang, Hulin Han, Ki-Seok Jang, Seung Sam Paik
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引用次数: 1

摘要

淋巴管平滑肌瘤(LAM)是一种罕见的良性肿瘤,其特征是在肺、纵隔和腹膜后淋巴管壁上有紊乱的平滑肌细胞增生。肠系膜LAM是一种很不寻常的表现。一名47岁女性因7年腹部肿块病史入住我院。计算机断层扫描显示一个边缘良好的肿块,软组织衰减。行腹腔镜切除。标本显示一个边界清楚的暗色囊性肿块。切面可见薄壁囊性肿瘤,伴有不规则分布的小梁状间隔。显微镜下,肿瘤显示大小不等的扩张空间,由扁平的内皮细胞排列,周围是上皮样细胞或梭形细胞。衬里细胞D2-40、CD31、CD34阳性。周围细胞α -平滑肌肌动蛋白和人黑色素瘤黑-45阳性。最终诊断为肠系膜单发LAM。术后10个月,患者表现平平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extrapulmonary lymphangioleiomyoma presenting as a mesenteric cystic mass

Lymphangioleiomyoma (LAM) is a rare benign tumor characterized by a disorganized smooth muscle cell proliferation within the walls of pulmonary, mediastinal, and retroperitoneal lymphatic vessels. The mesenteric LAM is a quite unusual presentation. A 47-year-old woman was admitted to our hospital with a 7-year history of abdominal mass. A computed tomography showed a well marginated mass with soft tissue attenuation. Laparoscopic excision was performed. The specimen revealed a well circumscribed dark cystic mass. The cut surface showed a thin walled cystic tumor with haphazardly distributed trabeculated septa. Microscopically, the tumor showed variable sized ectatic spaces lined by flattened endothelial cells and surrounded by epithelioid or spindle-shaped cells. The lining cells were positive for D2-40, CD31, and CD34. The surrounding cells were positive for alpha-smooth muscle actin and human melanoma black-45. The final diagnosis was a solitary LAM arising in the mesentery. The patient showed an uneventful postoperative course for 10 months.

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