Review series
Rare diseases
1
Lymphangioleiomyomatosis: clinical features, management and basic mechanisms
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. |
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Introduction |
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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
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