Abstract
Lymphangioleiomyomatosis (LAM) is a rare disease characterized by progressive cystic destruction of the lungs. We present an unusual radiological presentation of lymphangioleiomyomatosis in a patient followed for 33 years with profuse coarse lung nodules in addition to the classical cystic lesions. We believe that this report might support the case for considering LAM a low-malignant neoplasm.
Originalsprog | Engelsk |
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Tidsskrift | European Clinical Respiratory Journal |
Vol/bind | 1 |
DOI | |
Status | Udgivet - 2014 |