Abstract
Lymphangioleiomyomatosis is a rare pulmonary disorder that almost exclusively affects women of childbearing age. Histopathological findings of LAM are very similar to tuberous sclerosis, raising the possibility that LAM is a forme fruste of TS. Chest radiographic findings of LAM include large lung volumes with bilaterally symmetric linear and/or reticular abnormalities or direct visualization of the pulmonary cysts. HRCT in patients with LAM shows numerous thin-walled, regular cysts without a zonal predominance. Pleural effusions may occur in patients with LAM, and pneumothorax may be the presenting feature of the disease in a number of patients. The diagnosis of LAM may be established with transbronchial or surgical lung biopsy, although a tissue diagnosis may be avoided in patients with sufficiently characteristic clinical, laboratory, and HRCT findings.
Original language | English (US) |
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Pages (from-to) | 135-138 |
Number of pages | 4 |
Journal | Clinical Pulmonary Medicine |
Volume | 12 |
Issue number | 2 |
DOIs | |
State | Published - Mar 1 2005 |
Keywords
- Cyst
- High-resolution CT
- Langerhans cell histiocytosis
- Lymphangioleiomyomatosis
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine
- Critical Care and Intensive Care Medicine