Sažetak sa skupa
https://doi.org/10.26800/LV-145-supl2-CR40
Exceptionally large juvenile xanthogranuloma – a case report
Luka Bulić
; School of Medicine, University of Zagreb, Zagreb, Croatia
Eva Brenner
Suzana Ožanić Bulić
Sažetak
Juvenile xanthogranuloma (JXG) is a rare, benign skin lesion pathologically classified as a non-Langerhans cell histiocytosis. The lesions appear within
the first year of life in 75% of patients, predominantly on the head or neck, growing up to 5mm in size. While the etiology is mostly infectious, it can also be caused by genetic variants. In most patients, the condition has an easy course and resolution. Histopathological features include a histiocytic invasion of the superficial dermis, with additional eosinophils, lymphocytes and plasma cells. The lesion typically stains with anti-CD4, anti-XIIIa and CD68 markers.
Ključne riječi
child; juvenile xanthogranuloma; scalp
Hrčak ID:
303557
URI
Datum izdavanja:
23.4.2023.
Posjeta: 168 *