Lymphangioleiomyomatosis: a case report

Lymphangioleiomyomatosis (LAM) is a rare disease of unknown etiology affecting woman, primarily in their reproductive years. It is characterized by non-neoplasic proliferation of atypical smooth muscle cells that may lead to airway, lymphatic and blood vessel obstruction over time.A nine-year follow...

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Veröffentlicht in:Revista portuguesa de pneumologia 2005-11, Vol.11 (6), p.573-586
Hauptverfasser: Costa, Antonio Santos, Noya, Rafael, Calvo, Teresa Campos, Severo, R, Afonso, Abel
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Sprache:por
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Zusammenfassung:Lymphangioleiomyomatosis (LAM) is a rare disease of unknown etiology affecting woman, primarily in their reproductive years. It is characterized by non-neoplasic proliferation of atypical smooth muscle cells that may lead to airway, lymphatic and blood vessel obstruction over time.A nine-year followed-up case of LAM is described,which presents with some unusual details as worsening haemoptysis in the setting of pregnancy and absence of cough or pneumothorax along the course of the disease. Neither haemoptysis nor gradual pulmonary function deterioration seemed to be influenced by hormone therapy. A brief re-view of the disease is then presented.
ISSN:0873-2159