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Thorax 1999;54:254-264; doi:10.1136/thx.54.3.254
Copyright © 1999 BMJ Publishing Group Ltd & British Thoracic Society.
Thorax 1999;54:254-264 ( March )

Review series

Rare diseases bullet  1

Lymphangioleiomyomatosis: clinical features, management and basic mechanisms

Simon Johnson

Division of Respiratory Medicine, University of Nottingham, City Hospital, Hucknall Road, Nottingham NG5 1PB, UK

The first 150 words of the full text of this article appear below.

    Introduction

Lymphangioleiomyomatosis, a rare disease of unknown aetiology, affects women only. It mainly involves the lungs where, as its name suggests, lymphatics (lymph), blood vessels (angio), and airways are surrounded by smooth muscle (leiomyo) proliferation. It is characterised by progressive dyspnoea, haemoptysis, pneumothorax, and chylous pleural effusions and runs a variable course culminating usually in respiratory failure.1 2 Lymph nodes in the abdomen and pelvis may be involved and up to half the patients have renal angiomyolipomas. The disease usually arises spontaneously although it also occurs in some patients with tuberous sclerosis.3

Much of our knowledge of this unusual disorder is anecdotal, coming from case reports and reviews of patients attending tertiary referral centres, which may not represent the full spectrum of the disease. This will change over the next few years as patient registries are being compiled for research purposes in the United Kingdom, United . . . [Full text of this article]


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