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See Latest ArticlesSpumous histiocytic oligoarthritis coexisting with systemic Langerhans’ cell histiocytosis: Case report and literature review
Joint, Bone, Spine, 08/25/09
Aouba A et al. – A 27–year–old man consulted with clinical and radiological features of chronic erosive oligoarthritis of large joints (hips and knee), associated with diffuse lymph–node enlargement and diabetes insipidus. Lymph–node biopsy provided the diagnosis of systemic Langerhans’ cell histiocytosis.
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Macrophages in Langerhans cell histiocytosis are differentiated toward M2 phenotype: Their possible involvement in pathological processes
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High incidence of hearing loss in long-term survivors of multisystem langerhans cell histiocytosis
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CD30 positive anaplastic large-cell lymphoma mimicking Langerhans cell histiocytosis
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Neurodegenerative central nervous system Langerhans cell histiocytosis and coincident hydrocephalus treated with vincristine/cytosine arabinoside
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