Results 191 to 200 of about 9,825 (225)
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A unique non-Langerhans cell histiocytosis with some features of generalized eruptive histiocytoma
Journal of the American Academy of Dermatology, 1994A symmetric eruption of hundreds of coalescent small red macules and a few slightly elevated papules sparing the flexures was observed in a 73-year-old man. Light microscopic examination showed loose aggregates of small and large histiocytic cells. Electron microscopy showed an absence of Langerhans cell granules and lipid droplets.
S, Goerdt +5 more
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Blood, 2005
AbstractErdheim-Chester disease is a rare non-Langerhans histiocytosis with multisystem involvement. To date, there is no standard treatment for this disorder, and more than half of the patients succumb within 3 years. Because interferon-α promotes the terminal differentiation of histiocytes and dendritic cells, we hypothesized that this molecule would
Fadi, Braiteh +3 more
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AbstractErdheim-Chester disease is a rare non-Langerhans histiocytosis with multisystem involvement. To date, there is no standard treatment for this disorder, and more than half of the patients succumb within 3 years. Because interferon-α promotes the terminal differentiation of histiocytes and dendritic cells, we hypothesized that this molecule would
Fadi, Braiteh +3 more
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[Acquired regressive cutaneous non-Langerhans-cell histiocytosis in an infant].
Annales de dermatologie et de venereologie, 1998Cutaneous histiocytosis of childhood often regresses spontaneously without treatment. In some cases however, it is difficult to differentiate aggressive forms and electron microscopy and immunohistochemistry can be a valuable help. We report a case of cutaneous histiocytosis in a child which illustrates the difficulties encountered in the ...
M, Campourcy +6 more
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Non-langerhans Cell Histiocytosis-Including Erdheim-Chester Disease- and the Lung
2014Erdheim-Chester disease (ECD) is a rare form of non–Langerhans’ cell histiocytosis that may present with pulmonary involvement. The disease was first described as the “lipoid granulomatose” in 1930. Between then and 2013, more than 500 cases have been reported.
Julien Haroche +5 more
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[Clinicopathological study of non-Langerhans cell histiocytosis in central nervous system].
Zhonghua nei ke za zhi, 2016To explore the clinicopathological features and imaging characteristics of non-Langerhans cell histiocytosis in central nerve system, thus to facilitate the diagnosis and differential diagnosis.A total of ten cases were enrolled in the study, with seven cases of Rosai-Dorfman disease (RDD) and three cases of xanthoma disseminatum (XD).
Tingting, Zhang +4 more
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A Rare Presentation of a Rare Non-Langerhans Cell Histiocytosis
A74. RARE CASES IN THORACIC ONCOLOGY, 2023A.A. Velthottam Rathinam +2 more
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Langerhans cell and non Langerhans cell histiocytosis: So different?
2007The Author reports the clinical and laboratory criteria that do not support the strict distinction between Langerhans cell and non Langerhans cell histiocytosis as reported in the relevant literature.
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Non-Langerhans Cell Histiocytosis Mimicking Pulmonary Tuberculosis: A Case Report
B68. CURIOUS PRESENTATIONS: CANCERS AND MIMICKERS, 2022J.D. Botero Bahamon +2 more
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Non–Langerhans Cell Histiocytosis with Involvement of the Optic Disc and Retina
Ophthalmology Retina, 2022Vipin Rana, Renu Suthar, Deeksha Katoch
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Cutaneous Erythrodermatic Non-Langerhans Cell Histiocytosis in Childhood.
The American Journal of Dermatopathology, 1997K. Bosler, R. Linsc, K. Jung
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