Pregled bibliografske jedinice broj: 1279057
Exceptionally large juvenile xanthogranuloma – a case report
Exceptionally large juvenile xanthogranuloma – a case report // Liječnički vjesnik 2023, 145(Supp 2)
Zagreb, Hrvatska, 2023. str. 66-66 doi:10.26800/LV-145-supl2-CR40 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1279057 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Exceptionally large juvenile xanthogranuloma – a
case report
Autori
Bulić, Luka ; Brenner, Eva ; Ožanić Bulić, Suzana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Liječnički vjesnik 2023, 145(Supp 2)
/ - , 2023, 66-66
Skup
18th International Croatian Student Summit of Biomedical Students and Young Scientists
Mjesto i datum
Zagreb, Hrvatska, 25.04.2023. - 28.06.2023
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
child ; juvenile xanthogranuloma ; scalp
Sažetak
INTRODUCTION/OBJECTIVES: 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. CASE PRESENTATION: A 1-year-old female patient was examined for a large, solitary scalp lesion with features of JXG. The lesion started as a yellow erythematous plaque, measuring 17x13mm in size. Histopathological analysis showed histiocytes and occasional foam cells, lymphocytes, macrophages and multinuclear giant cells in the dermis. Immunodiagnostic tests returned positive for CD68 and negative for S100 and CD1a, confirming JXG. The patient attended three follow-up appointments, at which substantial growth of the lesion was observed. At the last examination, it measured 40mm in diameter. Topical corticosteroids were applied but didn’t affect the progression. CONCLUSION: This case of JXG is set apart by the size of the lesion, which is eight times larger than in the average patient. Since the patient had no prior infection or serious illness, it is worth raising the question of a genetic variant being the cause of the lesion, and how such a variant might have impacted its size.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinika za dječje bolesti