Abstract
Juvenile xanthogranuloma (JX) is a regressing fibrous histiocytoma occurring during infancy and characterized by cutaneous papules and nodules and less often by additional lesions in deep tissue and organs. It has a special place among childhood masses by presenting different outcomes and spontaneous regression. We report three cases of JX that were detected after birth and resected.
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References
Enzinger FM, Weiss SW (1988) Benign fibrohistiocytic tumors. In: Soft tissue tumors, 2nd end. Mosby, St Louis, pp 223–251
Helwig EB, Hackney VC (1954) Juvenile xanthogranuloma. Am J Pathol 30: 626
Nicholson DH, Green WR (1981) Juvenile xanthogranuloma (JXG). In: Pediatric ocular tumors, Masson, New York, pp 103–105
Singh R, Ghazal W (1992) Juvenile xanthogranuloma. Cutis 49: 347–348
Sonoda T, Hashimoto H, Enjoji M (1985) Juvenile xanthogranuloma: clinicopathologic analysis and immunohistochemical study of 57 patients. Cancer 56: 2280–2286
Webster SB, Reister HC, Harman LE Jr (1966) Juvenile xanthogranuloma with extracutaneous lesions Arch Dermatol 93: 71–76
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Görk, S., Aritürk, E., Bariş, S. et al. Juvenile xanthogranuloma: three cases. Pediatr Surg Int 11, 427–428 (1996). https://doi.org/10.1007/BF00497839
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DOI: https://doi.org/10.1007/BF00497839