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A CASE OF LYMPHANGIOLEIOMYOMATOSIS WITH MULTIPLE ANGIOMYOLIPOMAS IN THE KIDNEYS: A CASE REPORT

Authors :
Yong Kek Pang
Soon Hin How
Chong-Kin Liam
Azlin S
Source :
Journal of Health and Translational Medicine. 9:35-38
Publication Year :
2006
Publisher :
Univ. of Malaya, 2006.

Abstract

Lymphangioleiomyomatosis (LAM) is a rare disease. The reported prevalence is around one per million in the West but the exact prevalence in Asia is unknown. It affects primarily young women of reproductive age, with a mean age of onset at 34 years. The disease is characterised by an abnormal proliferation of smooth muscle-like cells that grow over a course of time to obstruct airways, lymphatic andblood vessels. We report a case of LAM in a young woman who presented with a spontaneous pneumothorax. Computed tomography scan of the thorax and abdomen showed homogenous thin-walled cystic lesions with normal intervening lung parenchyma and multiple lesions in her kidneys with Hounsfield units similar to that of fat.

Details

ISSN :
2289392X
Volume :
9
Database :
OpenAIRE
Journal :
Journal of Health and Translational Medicine
Accession number :
edsair.doi...........533936e4157f5a1ba90359dc70f86a87