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Histiocytosis X: VIII. Histiocytosis X Simulating Tuberculosis
Acta Radiologica: Oncology, 1983The findings in 9 patients with histiocytosis X localized to the spine and 7 patients with tuberculous spondylitis were compared. It was not always possible to differentiate between these two conditions without a supplementary fine needle aspiration biopsy.
P, Thommesen, N, Bartholdy, E, Bünger
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Pediatric Radiology, 1993
Congenital histiocytosis X involving multiple organs is a rare disease that causes rapid mortality in intrauterine and neonatal life. The diagnosis of histiocytosis X (Letterer-Siwe disease) should be considered in a neonate with vesiculated crusting skin lesions.
A, Vade, A, Hayani, K L, Pierce
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Congenital histiocytosis X involving multiple organs is a rare disease that causes rapid mortality in intrauterine and neonatal life. The diagnosis of histiocytosis X (Letterer-Siwe disease) should be considered in a neonate with vesiculated crusting skin lesions.
A, Vade, A, Hayani, K L, Pierce
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Lung, 1985
Pulmonary histiocytosis X is a granulomatous disorder of the lung of unknown cause. Patients with this disease often complain of cough, dyspnea on exertion, and, occasionally, chest pain from a pneumothorax or bone involvement. However, it is not unusual for patients to be asymptomatic with only a diffuse interstitial infiltrate on their chest ...
T W, Marcy, H Y, Reynolds
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Pulmonary histiocytosis X is a granulomatous disorder of the lung of unknown cause. Patients with this disease often complain of cough, dyspnea on exertion, and, occasionally, chest pain from a pneumothorax or bone involvement. However, it is not unusual for patients to be asymptomatic with only a diffuse interstitial infiltrate on their chest ...
T W, Marcy, H Y, Reynolds
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Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina, 1996
Histiocytosis X comprises a spectrum of diseases of unknown etiology in which localized or systemic histiocytic proliferations occur, often associated with eosinophilic infiltration of the involved tissues. The three clinical syndromes are: eosinophilic granuloma, Hand-Schuller-Christian disease and Abta-Letteres-Siwesche's disease.
L, Grzybowska, P, Tutka
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Histiocytosis X comprises a spectrum of diseases of unknown etiology in which localized or systemic histiocytic proliferations occur, often associated with eosinophilic infiltration of the involved tissues. The three clinical syndromes are: eosinophilic granuloma, Hand-Schuller-Christian disease and Abta-Letteres-Siwesche's disease.
L, Grzybowska, P, Tutka
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BRAFV600E-induced senescence drives Langerhans cell histiocytosis pathophysiology
Nature Medicine, 2021Camille Bigenwald +2 more
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