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Lymphangioleiomyomatosis [PDF]

open access: bronzeEuropean Respiratory Journal, 2006
Lymphangioleiomyomatosis (LAM) is a rare disease of the lungs and lymphatics, which can occur sporadically or in association with tuberous sclerosis. LAM almost exclusively affects females, generally developing before the menopause.The disease is characterised by progressive pulmonary cystic change, recurrent pneumothorax, chylous pleural collections ...
Simon R. Johnson
  +11 more sources

Brazilian Thoracic Association recommendations for the management of lymphangioleiomyomatosis [PDF]

open access: yesJornal Brasileiro de Pneumologia
Lymphangioleiomyomatosis (LAM) is a rare disease, characterized as a low-grade neoplasm with metastatic potential that mainly affects women of reproductive age, in which there is proliferation of atypical smooth muscle cells (LAM cells) and formation of ...
Bruno Guedes Baldi   +13 more
doaj   +2 more sources

Uterine lymphangioleiomyomatosis in a premenopausal woman with tuberous sclerosis: A case report [PDF]

open access: yesCase Reports in Women's Health
Lymphangioleiomyomatosis is a rare disease characterized by abnormal smooth muscle cell growth. It primarily occurs in the lungs but can also rarely occur in other organs, in which case it is classified as extrapulmonary lymphangioleiomyomatosis.
Eun Min Lee   +3 more
doaj   +2 more sources

Lung transplantation for lymphangioleiomyomatosis. N [PDF]

open access: bronzeJournal of Bronchology, 1997
Lymphangioleiomyomatosis is a rare disease of unknown origin that usually leads to progressive deterioration of lung function and eventual death from respiratory failure. It occurs in women of reproductive age and people with tuberous sclerosis. Lung transplantation is a recent therapeutic approach.We conducted a retrospective study by questionnaire of
A. Boehler   +3 more
openalex   +4 more sources

Lymphangioleiomyomatosis

open access: hybridPresse medicale (Paris, France : 1983), 2010
Lymphangioleiomyomatosis is caused by mutations (usually sporadic, sometimes in tuberous sclerosis) of the TSC1 or TSC2 genes and results in cystic destruction of the lungs, with CT features being sufficiently characteristic to establish the diagnosis in many cases. Two-thirds of patients suffer pneumothoraces.
Yusra Sheikh, Andrew Dixon
  +5 more sources

A challenging convergence of conditions in a patient with thalassemia major presenting with thymoma and lymphangioleiomyomatosis: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background β-Thalassemia major is a complex, multisystemic condition. Effective transfusion programs, optimal iron chelation therapy, and progresses in magnetic resonance imaging have significantly improved patient survival.
Aldo Carnevale   +6 more
doaj   +2 more sources

Abdominal lymphangioleiomyomatosis in a man presenting with gastrointestinal hemorrhage as the first manifestation: a case report [PDF]

open access: yesFrontiers in Medicine
Lymphangioleiomyomatosis (LAM) is a rare, low-grade malignant condition that typically affects women of childbearing age and primarily involves the lungs. While cases involving males and affecting the gastrointestinal tract are exceedingly uncommon. This
Ying Zi, Yuchen Shi, Rongjie Shi
doaj   +2 more sources

Lymphangioleiomyomatosis

open access: yesLa Presse Médicale, 2023
Lymphangioleiomyomatosis (LAM) is an ultra-rare, slowly progressive neoplastic cystic disease, belonging to the group of PEComas. It can occur sporadically or associated to tuberous sclerosis complex disease and affects mainly women in child-birth age.
Elia, Davide   +4 more
openaire   +4 more sources

Lymphangioleiomyomatosis [PDF]

open access: yesKlinicka Onkologie, 2019
Lymphangioleiomyomatosis (LAM) is a rare systemic disease that occurs sporadically (S/LAM) or as part of tuberous sclerosis (TS/LAM). LAM is characterized by proliferation of abnormal smooth muscle cells. This disease clinically manifests as dyspnea on exertion and pneumothorax.
Martina, Doubková   +4 more
openaire   +4 more sources

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