JUVENILE XANTHOGRANULOMA: REPORT OF A CASE

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Juvenile Xanthogranuloma: Report of a Case.

JUVENILE xanthogranuloma, also commonly known as naevoxantho-endothelioma, was first described as a skin disease in 1909 (McDonaugh, 1909), but it was not until forty years later that the first intra-ocular case was reported in America (Blank, Eglick, and Beerman, 1949). Some twenty to thirty cases have since been described (Sanders, 1962), but our case is the first to be reported in the United...

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juvenile xanthogranuloma of the hand: a case report

conclusions juvenile xanthogranuloma is a cutaneous fibrohistiocytic lesion, which is rarely reported on palms. it is recommended to excise any soft tissue masses in children due to their possible association with malignancy. introduction juvenile xanthogranuloma (jxg) is a non-langerhans-cell histiocytosis, a group of histiocytic proliferative disorders, seen throughout the first two decades o...

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Lingual juvenile xanthogranuloma in a woman: a case report

INTRODUCTION Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder. Extracutaneous sites are rare. CASE PRESENTATION We present a rare case of oral juvenile xanthogranuloma in a 49-year-old Caucasian woman. The histopatholog...

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Juvenile xanthogranuloma of the ear: A case report.

Juvenile xanthogranuloma is a relatively uncommon, benign histiocytic proliferative disorder. A case of juvenile xanthogranuloma in a 13-month-old girl with an unusual clinical form is described. She presented with a yellow-red projecting nodule over the helical rim of her right ear. The lesion was histologically diagnosed as juvenile xanthogranuloma after excisional biopsy. Although primarily ...

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Solitary juvenile xanthogranuloma with tibial involvement: a case report.

Juvenile xanthogranuloma (JXG) is a rare disease that is part of a spectrum of histiocytic dendritic cell disorders. Most patients present with a solitary cutaneous lesion; however, others present with extracutaneous manifestations or even with systemic involvement. We present the first report of an 11-month-old girl in whom was diagnosed a unifocal extracutaneous JXG involving the tibia. Histo...

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ژورنال

عنوان ژورنال: British Journal of Ophthalmology

سال: 1965

ISSN: 0007-1161

DOI: 10.1136/bjo.49.2.71