Results 211 to 220 of about 11,099 (227)
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La 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
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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
Clinics in Chest Medicine, 2004
Lymphangioleiomyomatosis (LAM) is a rare idiopathic disease predominately affecting women. The disease is characterized by peribronchial, perivascular, and perilymphatic proliferation of smooth muscle like cells resulting in vascular and airway obstruction and cyst formation.
Rudan, Diana, Stipić-Marković, Asija
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Lymphangioleiomyomatosis (LAM) is a rare idiopathic disease predominately affecting women. The disease is characterized by peribronchial, perivascular, and perilymphatic proliferation of smooth muscle like cells resulting in vascular and airway obstruction and cyst formation.
Rudan, Diana, Stipić-Marković, Asija
+6 more sources
Clinics in Chest Medicine, 2016
Lymphangioleiomyomatosis is a rare multisystem disease predominantly affecting women that can occur sporadically or in association with tuberous sclerosis. Lung cysts progressively replace the lung parenchyma, which leads to dyspnea, recurrent pneumothorax, and in some cases respiratory failure.
Simon R, Johnson +2 more
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Lymphangioleiomyomatosis is a rare multisystem disease predominantly affecting women that can occur sporadically or in association with tuberous sclerosis. Lung cysts progressively replace the lung parenchyma, which leads to dyspnea, recurrent pneumothorax, and in some cases respiratory failure.
Simon R, Johnson +2 more
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The American Journal of the Medical Sciences, 2001
Lymphangioleiomyomatosis (LAM), a rare disorder of unknown cause that occurs almost exclusively in women of childbearing years, is characterized microscopically by abnormal smooth muscle proliferation in the lung, lymphatics, and mediastinal, abdominal and lower cervical lymph nodes. LAM is associated with progressive dyspnea, recurrent pneumothoraces,
J, Kelly, J, Moss
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Lymphangioleiomyomatosis (LAM), a rare disorder of unknown cause that occurs almost exclusively in women of childbearing years, is characterized microscopically by abnormal smooth muscle proliferation in the lung, lymphatics, and mediastinal, abdominal and lower cervical lymph nodes. LAM is associated with progressive dyspnea, recurrent pneumothoraces,
J, Kelly, J, Moss
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Pulmonary lymphangioleiomyomatosis
The Japanese Journal of Thoracic and Cardiovascular Surgery, 2006We report a case of lymphangioleiomyomatosis (LAM) in a 33-year-old woman. Left pneumothorax was noted during a physical checkup at a local clinic. Multiple bullae in the bilateral lungs were also seen on chest computed tomography. Therefore, she underwent surgery for diagnosis and therapy. A large number of cysts of various sizes were seen in the left
Seiji, Okimasa, Satoshi, Shibata
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Presse medicale (Paris, France : 1983), 2010
La lymphangioléiomyomatose est une maladie pulmonaire rare rencontrée quasi exclusivement chez la femme en période d’activité génitale. L’atteinte pulmonaire est caractérisée par des kystes pulmonaires multiples à parois fines, des pneumothorax récidivants, un trouble ventilatoire obstructif, et une évolution vers l’insuffisance respiratoire chronique ...
Cottin, Vincent +4 more
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La lymphangioléiomyomatose est une maladie pulmonaire rare rencontrée quasi exclusivement chez la femme en période d’activité génitale. L’atteinte pulmonaire est caractérisée par des kystes pulmonaires multiples à parois fines, des pneumothorax récidivants, un trouble ventilatoire obstructif, et une évolution vers l’insuffisance respiratoire chronique ...
Cottin, Vincent +4 more
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Pulmonary Lymphangioleiomyomatosis
Journal of Computer Assisted Tomography, 1981A case of pulmonary lymphangioleiomyomatosis is reported and the computed tomographic findings are described. The disease is characterized by chylous pleural effusions, a reticulonodular pattern, and the development of air trapping with bullous formation. Computed tomography is useful in demonstrating the early presence of these bullae and in excluding
J L, Berger, M I, Shaff
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Unilateral Lymphangioleiomyomatosis
Journal of Thoracic Imaging, 2005Pulmonary involvement in tuberous sclerosis complex (TSC) resembles lymphangioleiomyomatosis (LAM) in its clinical, radiologic, and histopathological features. Typical high-resolution computed tomography (HRCT) findings are of bilateral thin-walled cysts symmetrically throughout both lungs, with associated increase in lung volumes.
Audrey Eleanor Therese, Wenaden +1 more
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Pulmonary lymphangioleiomyomatosis
Pathology, 1994This paper reports a case of a 50 yr old premenopausal woman with pulmonary lymphangioleiomyomatosis. This asymptomatic woman was found to have 'pulmonary nodules' on routine chest x-ray simulating metastatic lesions. The final diagnosis was possible after pathological examination of the lung biopsy specimens.
A, Firouz-Abadi, J P, Higgins
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