Lymphangioleiomyomatosis: what do we know and what are we looking for?

Abstract

Lymphangioleiomyomatosis (LAM) is a rare disease characterised by proliferation of abnormal smooth muscle-like cells (LAM cells) leading to progressive cystic destruction of the lung, lymphatic abnormalities and abdominal tumours. It affects predominantly females and can occur sporadically or in patients with tuberous sclerosis complex. This review describes the recent progress in our understanding of the molecular pathogenesis of the disease and LAM cell biology. It also summarises current therapeutic approaches and the most promising areas of research for future therapeutic strategies.

• Authors: S Harari, O Torre, J Moss
• Journal: European respiratory review : an official journal of the European Respiratory Society (Eur Respir Rev) Vol. 20 Issue 119 Pg. 34-44 (Mar 2011) ISSN: 1600-0617 [Electronic] England
• PMID: 21357890 (Publication Type: Journal Article, Research Support, N.I.H., Intramural, Review)

Topics

• Cell Proliferation
• Diagnosis, Differential
• Female
• Gene Expression Regulation
• Humans
• Lung (diagnostic imaging, metabolism, pathology)
• Lymphangioleiomyomatosis (diagnostic imaging, etiology, genetics, metabolism, pathology, therapy)
• Magnetic Resonance Imaging
• Myocytes, Smooth Muscle (diagnostic imaging, metabolism, pathology)
• Predictive Value of Tests
• Risk Factors
• Sex Factors
• Signal Transduction
• Tomography, X-Ray Computed
• Treatment Outcome
• Tuberous Sclerosis (complications)