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http://dx.doi.org/10.1080/00015559850135904 | DOI Listing |
J Eur Acad Dermatol Venereol
March 2023
Department of Dermatology, Venereology and Allergology, Academic Teaching Department of Medical University Innsbruck, Central Hospital Bolzano/Bozen, Bolzano, Italy.
JAAD Case Rep
January 2022
Department of Dermatology, Baylor College of Medicine, Houston, Texas.
Pediatr Dermatol
September 2018
Department of Dermatology, University of California, San Francisco, CA, USA.
Background/objectives: Congenital juvenile xanthogranulomas are infrequently described in the medical literature. We report three previously unpublished cases and systematically review the literature to better characterize this variant.
Methods: We surveyed English-language articles indexed in MEDLINE (1951-March 2017) and EMBASE (1974-March 2017) for cases of congenital-onset juvenile xanthogranulomas confirmed on histopathology.
Dermatol Online J
October 2016
Department of Medicine, Division of Dermatology, University of California Los Angeles (UCLA), Los Angeles, California.
Juvenile xanthogranuloma (JXG) is a benign, non-Langerhans cell histiocytosis, which commonly manifests as a solitary papule or nodule in infants and young children. However, other less common clinical presentations have been reported including clustered, agminated or plaque-like. It is important to recognize these variants, as diagnosis is often clinical.
View Article and Find Full Text PDFPediatr Dermatol
August 2014
Department of Dermatology, Instituto Valenciano de Oncologia, Valencia, SpainDepartment of Dermatology, Hospital General Universitario de Valencia, SpainDepartment of Pathology and Hospital del Niño Jesús, Madrid, SpainDepartment of Dermatology, Hospital del Niño Jesús, Madrid, Spain.
Clustered or agminated juvenile xanthogranuloma (JXG) is an unusual form of JXG characterized by multiple reddish-brown or yellowish papules and nodules in a coalescent pattern. We report a case of clustered JXG involving the left lower back of a 5-month-old boy.
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