Juvenile xanthogranuloma: Case report; [Juvenil ksantogranülom]

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dc.contributor.authorGençoǧlan G.
dc.contributor.authorInanir I.
dc.contributor.authorDemireli P.
dc.contributor.authorŞencan A.
dc.contributor.authorAygören S.R.
dc.date.accessioned2024-07-22T08:20:47Z
dc.date.available2024-07-22T08:20:47Z
dc.date.issued2010
dc.description.abstractJuvenile xanthogranuloma is an uncommon non-Langerhans cell histiocytosis of infancy and childhood. Etiology is not clear. This benign disorder characterized by solitary or multiple yellow-red papulonodules on the skin can occasionally be observed in other organs. They generally appear as reddish-yellow papules which enlarge up to 1 cm in diameter and evolve into yellow-brown plaques and macules. Prognosis is good and lesions mostly improve spontaneously. In this paper, an eleven-month-old boy who admitted with a nodule on the scalp is presented. The possible systemic organ involvement and accompanying diseases were evaluated. No treatment was performed and regular follow-up was planned. Since the lesion did not regress spontaneously during the three months and caused discomfort, total excision was performed. Diagnosis of JXG was confirmed histopathologically. Copyright © 2010 by Türkiye Klinikleri.
dc.identifier.issn13000381
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/18326
dc.language.isoTurkish
dc.subjectarticle
dc.subjectcase report
dc.subjectclinical feature
dc.subjectexcision
dc.subjecthistopathology
dc.subjecthuman
dc.subjecthuman tissue
dc.subjectinfant
dc.subjectjuvenile xanthogranuloma
dc.subjectmale
dc.subjecttreatment outcome
dc.titleJuvenile xanthogranuloma: Case report; [Juvenil ksantogranülom]
dc.typeArticle

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