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Langerhans cell histiocytosis [PDF]
The 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
doaj +3 more sources
J S Pegum, Patricia Wallis
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Quantitative Brain MRI Analysis in Neurodegenerative Langerhans Cell Histiocytosis. [PDF]
ABSTRACT Background Neurodegenerative Langerhans Cell Histiocytosis (ND‐LCH) is a severe central nervous system involvement complicating LCH. ND‐LCH is characterized by a cerebellar ataxia, pyramidal signs, pseudobulbar palsy, cognitive impairment, and behavioral disturbances.
Baek C+18 more
europepmc +2 more sources
Histiocytosis X of the Hypothalamus
Abstract An 18-year-old woman presented with visual disturbance and endocrine dysfunction (diabetes insipidus, delayed puberty, hypothyroidism, hypoadrenalism, and hyperprolactinemia). Computed tomography and enhanced cisternography showed a single hypothalamic mass, which proved at biopsy to be histiocytosis X.
K. Patrick Ober+4 more
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Histiocytosis X--current controversies. [PDF]
Valerie Broadbent, Jon Pritchard
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Commentary: "Histiocytosis X" [PDF]
Pulmonary Langerhans’ cell granulomatosis (LCG) is a diffuse, smoking-related lung disease characterised pathologically by bronchiolocentric inflammation, cyst formation, and widespread vascular abnormalities, and physiologically by exercise limitation. Pulmonary fibrosis is a long term sequel.
Dinah V. Parums
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Severe pulmonary hypertension in histiocytosis X: long-term improvement with bosentan [PDF]
L. Kiakouama+5 more
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Langerhans Histiocytosis Mimicking Aggressive Periodontitis in Adult: A Rare Case Report
Langerhans cell histiocytosis (LCH), also known as histiocytosis X, is a rare condition characterized by neoplastic proliferation of histiocytes and other inflammatory cells leading to the accumulation and pathological dissemination of histiocytes and ...
Rinku Sreekumar+2 more
doaj +2 more sources
Review of histiocytosis-X. [PDF]
P. T. Bray
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