Literature DB >> 19944562

[Lymphangioleiomyomatosis].

Vincent Cottin1, Fabienne Archer, Chahéra Khouatra, Romain Lazor, Jean-François Cordier.   

Abstract

Lymphangioleiomyomatosis is a rare pulmonary disease encountered almost exclusively in women of reproductive age. Pulmonary involvement is characterized by multiple thin-walled cysts in the lungs, recurrent pneumothorax, obstructive lung disorders, and progression to chronic respiratory failure over a mean period of 10 years. Certainty of diagnosis requires a lung biopsy, but international criteria have been proposed for a diagnosis without such a biopsy. International recommendations were recently issued for the diagnosis and treatment of lymphangioleiomyomatosis. Treatment is principally symptomatic and relies on the management of bronchial obstruction by bronchodilators; of hypoxemia by oxygen therapy; of pleural complications by pleurodesis, most often surgical; and of renal angiomyolipomas by percutaneous embolization in cases of hemorrhagic risk. Hormone treatment is not recommended. Hopes are high for mTor inhibitors (sirolimus and everolimus) and treatment trials are currently underway. Lung transplantation must be considered when chronic respiratory failure occurs in patients younger than 60 years. Copyright 2009 Elsevier Masson SAS. All rights reserved.

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Year:  2009        PMID: 19944562     DOI: 10.1016/j.lpm.2009.10.006

Source DB:  PubMed          Journal:  Presse Med        ISSN: 0755-4982            Impact factor:   1.228


  2 in total

1.  [Pulmonary lymphangioleiomyomatosis of unusual revelation during multiple sclerosis].

Authors:  Neirouz Ghannouchi Jaafoura; Ahmed Guigua; Houneida Zaghouani; Amira Atig; Dajla Bakir; Mabrouk Khalifa; Fethi Bahri
Journal:  Pan Afr Med J       Date:  2015-04-23

2.  Pulmonary lymphangioleiomyomatosis (LAM): A literature overview and case report.

Authors:  Cung-Van Cong; Tran-Thi Tuan Anh; Tran-Thi Ly; Nguyen Minh Duc
Journal:  Radiol Case Rep       Date:  2022-03-21
  2 in total

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