Lymphangioleiomyomatosis: solitary abdominal manifestation (2009: 9b)

被引:0
|
作者
Anne-Kristin Possekel
Detlef Katenkamp
Hans-Jürgen Brambs
Sandra Pauls
机构
[1] University Hospital of Ulm,Department of Diagnostic and Interventional Radiology
[2] University Hospital Jena,Department of Pathology
来源
European Radiology | 2009年 / 19卷
关键词
Lymphangioleiomyomatosis; Computed tomography; Sirolimus therapy;
D O I
暂无
中图分类号
学科分类号
摘要
Lymphangioleiomyomatosis (LAM) is a rare disease that usually affects premenopausal woman and is characterized by cystic lung lesions and lymphatic disorders. We report a case of a 23-year-old woman who presented with diffuse, but increasing abdominal pain. Transabdominal ultrasound showed multiple cystic formations. Due to the patient’s uncharacteristic symptoms, an exploratory laparotomy with tissue sampling was performed, and the diagnosis of LAM was confirmed by two independent pathologists. With computed tomography a broad abdominal, but no pulmonary, manifestation could be established. During sirolimus therapy the patient showed clinical benefit, but only slight progress in computed tomography.
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页码:3015 / 3018
页数:3
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