Results 51 to 60 of about 7,686 (174)
Rare Tumors, 2017 Langerhans cell sarcoma of the skin is a rare tumor with aggressive behavior. There are reports of Langerhans cell sarcoma involving the skin in patients with underlying systemic Langerhans cell histiocytosis.
Alejandro Peralta Soler +2 more
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Immunotherapy of Histiocytosis-X
Hematology/Oncology Clinics of North America, 1987 This article focuses on the interaction of histiocytosis-X and the immunotherapeutic agent, suppression. Studies with this and other agents have presented us with invaluable insights into the nature of histiocytosis-X.
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Commentary: "Histiocytosis X" [PDF]
Thorax, 1998 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.
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Langerhans cell histiocytosis presented as bilateral otitis media and mastoiditis
The Turkish Journal of Pediatrics, 2008 Langerhans cell histiocytosis (LCH) is a rare disease that may affect multiple organs. The etiology of LCH remains unclear to date. It is currently believed that clonal accumulation and proliferation of CD1a-positive Langerhans cells are causative.
Charalampos E Skoulakis +5 more
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Langerhans cell histiocytosis with pulmonary involvement and unilateral pneumothorax
The Turkish Journal of Pediatrics, 2010 Langerhans cell histiocytosis (LCH) is a rare disorder of Langerhans cell with unknown etiology, which can uncommonly be associated with pneumothorax.
Ghamartaj Khanbabaee +5 more
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Langerhans cell histiocytosis of the hip in children
The Pan African Medical Journal, 2019 Eight year old girl was referred to our consultation for a lameness with a flessum of the left hip with fever (38.5,C). Biology showed an inflammatory syndroma (CRP: 29 mg/l).
Zied Jlalia, Dhia Kaffel
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Journal of Spinal Surgery, 2014 Background: Langerhan's cell histiocytosis (LCH), previously known as histiocytosis X, is a reactive proliferative dendritic cells of unknown pathogenesis characterized by the proliferation of Langerhan's cells and is extremely rare in the lumbar spines ...
Rully H Dahlan +6 more
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Clinicopathological Features, Treatment Response, and Outcome of Rosai‐Dorfman Disease in Two Children [PDF]
Clin Case RepABSTRACT Rosai‐Dorfman disease is a rare non‐Langerhans cell histiocytic disorder. It is common in male children and young adults of African descent. It is classified into sporadic and familial types. The most common clinical presentation is massive bilateral cervical lymphadenopathy associated with constitutional symptoms. Histiocytic emperipolesis is
Evele G, Francine K.
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Adult onset asynchronous multifocal eosinophilic granuloma of bone: an 11-year follow-up
Acta Radiologica Open, 2015 Multifocal eosinophilic granuloma (EG) is a rare observation within the spectrum of histiocytosis X, generally described in children. We report the case of a 33-year-old man with multifocal EG showing an asynchronous evolution of bone lesions during a ...
Benjamin Dallaudière +4 more
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