Results 171 to 180 of about 6,813 (202)

Unilateral Lymphangioleiomyomatosis

Journal of Thoracic Imaging, 2005
Pulmonary 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, Susan Jennifer, Copley   +1 more
openaire   +2 more sources

Pulmonary Lymphangioleiomyomatosis

Journal of Computer Assisted Tomography, 1981
A 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
openaire   +2 more sources

Pulmonary lymphangioleiomyomatosis

Pathology, 1994
This 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
openaire   +2 more sources

Lymphangioleiomyomatosis: A review

European Journal of Internal Medicine, 2008
Lymphangioleiomyomatosis (LAM) is a rare disease, of unknown etiology, affecting women almost exclusively. Microscopically, LAM consists of a diffuse proliferation of smooth muscle cells. LAM can occur without evidence of other disease (sporadic LAM) or in conjunction with tuberous sclerosis complex (TSC).
Donald W, Hohman, Dena, Noghrehkar, Saman, Ratnayake   +2 more
openaire   +2 more sources

Chylothorax in Lymphangioleiomyomatosis*

Chest, 2003
Pulmonary lymphangioleiomyomatosis (LAM) is a rare, serious disorder characterized by proliferation of abnormal smooth-muscle cells and affects almost exclusively women of childbearing age. Optimal management of chylothorax, a well-recognized complication of LAM, in these patients has not been defined.
Jay H, Ryu, Clint H, Doerr, Susan D, Fisher, Eric J, Olson, Steven A, Sahn   +4 more
openaire   +2 more sources

Lymphangiogenesis in Lymphangioleiomyomatosis

American Journal of Surgical Pathology, 2004
Lymphangioleiomyomatosis (LAM) is characterized by the proliferation of abnormal smooth muscle cells (LAM cells) in the lungs, lymph nodes, and/or other organs. We examined lymphangiogenesis using immunohistochemistry for Flt-4 (VEGFR-3), a new specific marker for lymphatic endothelial cells, as well as the expression of vascular endothelial growth ...
Toshio, Kumasaka, Kuniaki, Seyama, Keiko, Mitani, Teruhiko, Sato, Sanae, Souma, Takashi, Kondo, Seiji, Hayashi, Masato, Minami, Toshimasa, Uekusa, Yoshinosuke, Fukuchi, Koichi, Suda   +10 more
openaire   +2 more sources

Lymphangioleiomyomatosis

Chest, 2008
Cory M. Yamashita, David Lynch, Gregory P. Downey   +2 more
openaire   +3 more sources

Lymphangioleiomyomatosis

New England Journal of Medicine, 2018
Alyssa, Sclafani, Paul, VanderLaan
openaire   +2 more sources

Lymphangioleiomyomatosis: a metastatic lung disease

American Journal of Physiology - Cell Physiology, 2023
Marina Holz, Nandini Kundu
exaly  

CrossTORC and WNTegration in Disease: Focus on Lymphangioleiomyomatosis

International Journal of Molecular Sciences, 2021
Vera Krymskaya
exaly