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Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
Published on: May 1, 2015
Lymphangioleiomyomatosis: A Review
Mohammed Amine Bouanzoul1, Yale Rosen2
1From the Department of Pulmonology and Phthisiology, Rouiba Hospital, University of Algiers, Rouiba, Algiers, Algeria (Bouanzoul).
Lymphangioleiomyomatosis (LAM) is a rare lung disease affecting women, characterized by abnormal cell growth. Recent advancements improve diagnosis and management, highlighting a shift towards minimally invasive procedures and clinical laboratory roles.
Area of Science:
- Pulmonary Medicine
- Oncology
- Genetics
Background:
- Lymphangioleiomyomatosis (LAM) is a rare multisystem neoplasm with perivascular epithelioid cell differentiation.
- Primarily affecting women of childbearing age, LAM involves lung compartment smooth muscle cell proliferation, leading to cystic destruction and potential respiratory failure.
- LAM cells harbor tuberous sclerosis (TSC) gene mutations and are influenced by female hormones like estrogens.
Purpose of the Study:
- To review recent advancements in LAM pathogenesis and diagnosis.
- To illustrate characteristic pathologic and radiologic findings.
- To discuss evidence-based therapies and emphasize multidisciplinary care.
Main Methods:
- A comprehensive literature review was conducted.
- Pertinent medical literature published in English over the last 30 years was analyzed.
Main Results:
- Significant progress has been made in understanding LAM pathophysiology and management.
- Current diagnostic trends favor minimally invasive procedures.
- The role of the clinical laboratory in LAM diagnosis is increasing.
Conclusions:
- Gaps remain in understanding LAM pathophysiology and immune system involvement.
- Minimally invasive diagnostic approaches are becoming standard care.
- Clinical laboratories will play a greater diagnostic role, potentially reducing surgical pathologist involvement in pulmonary LAM diagnosis.
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