Results 71 to 80 of about 8,935 (206)
São Paulo Medical JournalThe authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations.
Maria de Lourdes L. F. Chauffaille +10 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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Severe pulmonary hypertension in histiocytosis X: long-term improvement with bosentan: Table 1– [PDF]
, 2010 L. Kiakouama +5 more
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Infantile histiocytosis X (letterer-siwe disease).Investigations with enzymehistochemical and sheep-erythrocyte rosetting techniques [PDF]
, 1978 J. D. Elema, S Poppema
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Langerhans' Cell Histiocytosis (Histiocytosis X) of the Temporal Bone
, 2007 Dongxiao Nong +3 more
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Langerhans cell histiocytosis of the sphenoid sinus: a case report
The Turkish Journal of Pediatrics, 2010 Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare disorder characterized by clonal proliferation and excess accumulation of pathologic Langerhans cells causing local or systemic effects.
Guohua Yu +5 more
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Histiocytosis X and Pericarditis - A Rare Association and a Difficult Diagnosis. [PDF]
Curr Health Sci J, 2016 Tica I, Seceleanu M, Tica AA, Tica VI.
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Multifocal eosinophilic granuloma of bone causing unilateral proptosis
Indian Journal of Ophthalmology, 1987 The most benign expression of the disease histiocytosis X is eosinophilic granuloma of bone. The most common presentation is a solitary granuloma as originally described by. Lichtenstein [1]. Multiple involvement and orbital involvement is extremely rare
Pratap V +3 more
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