Adult Xanthogranuloma, Reticulohistiocytosis, and Rosai-Dorfman Disease.
| Autor: | Chisolm SS; Department of Dermatology, UCSF, 1701 Divisadero Street, San Francisco, CA 94115, USA., Schulman JM; Department of Dermatology, UCSF, 1701 Divisadero Street, San Francisco, CA 94115, USA; Department of Pathology, UCSF, 1701 Divisadero Street, San Francisco, CA 94115, USA., Fox LP; Department of Dermatology, UCSF, 1701 Divisadero Street, San Francisco, CA 94115, USA. Electronic address: FoxLi@derm.ucsf.edu. |
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| Jazyk: | angličtina |
| Zdroj: | Dermatologic clinics [Dermatol Clin] 2015 Jul; Vol. 33 (3), pp. 465-72; discussion 473. |
| DOI: | 10.1016/j.det.2015.03.011 |
| Abstrakt: | Adult xanthogranuloma presents most commonly as an orange-tan firm solitary nodule with no systemic manifestations. Recently, some cases have been reported in conjunction with lymphoproliferative disorders. Adult reticulohistiocytosis classically presents as red to yellow-red dermal nodules. In the multicentric form, lesions have a predilection for hands and elbows, with a classic coral bead periungual presentation, and are often associated with symmetric erosive arthritis, particularly of the hands and wrists. The presentation and course of Rosai-Dorfman disease, or sinus histiocytosis with massive lymphadenopathy, can vary. The classic presentation is extensive, painless bilateral cervical lymphadenopathy, but some cases have been entirely extranodal. (Copyright © 2015 Elsevier Inc. All rights reserved.) |
| Databáze: | MEDLINE |
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