Journal of Indian Society of Periodontology, 2011 Langerhans cell histiocytosis (LCH) is a group of rare disorders histologically characterized by the proliferation of Langerhans cells. Multiple organs and systems may be involved by the disease. Typically, there is bone involvement and, less frequently, lesions may be found in the lungs, liver, lymph nodes, skin, and mucosa.
Sushma Galgali +3 more
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Langerhans' Cell Histiocytosis
Dermatology Online Journal, 2002 Adult onset Langerhans cell histiocytosis is uncommon. A 29 year old man is presented who developed classic cutaneous disease with severe systemic involvement. He responded completely to a two month course of thalidomide.
Mortazavi, Hessein +3 more
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Rod-like tubular structures in the cytoplasm of histiocytes in “histiocytosis X” [PDF]
, 1968 Jie Man
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Histiocytosis-X:A case report with electron microscopic observations [PDF]
, 1966 Raymond A. Ritter
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Clinical, histochemical, and electron microscopic study of colonic histiocytosis. [PDF]
, 1966 Fred E. Pittman +4 more
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Sinus histiocytosis with massive lymphadenopathy: A pseudolymphomatous benign disorder.Analysis of 34 cases [PDF]
, 1972 Juan Rosaí, Ronald F. Dorfman
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Ultrastructural examination of broncho-alveolar lavage for diagnosis of pulmonary histiocytosis X: Preliminary report on 4 cases. [PDF]
, 1977 F Basset +3 more
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Benign sinus histiocytosis with massive lymphadenopathy: transient immunological defects in a child with mediastinal involvement [PDF]
, 1973 D. M. O. Becroft +4 more
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Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick disease. [PDF]
, 1979 Norman Dewhurst +3 more
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