Pregled bibliografske jedinice broj: 916622
Syringocystadenoma papilliferum: a rare tumor in an unusual location
Syringocystadenoma papilliferum: a rare tumor in an unusual location // Central European journal of paediatrics, 11 (2015), 1; 50-53 doi:10.5457/p2005-114.109 (recenziran, prikaz, stručni)
CROSBI ID: 916622 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Syringocystadenoma papilliferum: a rare tumor in an unusual location
Autori
Roganović, Jelena ; Brgodac, Ela ; Jonjić, Nives
Izvornik
Central European journal of paediatrics (2490-3671) 11
(2015), 1;
50-53
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, prikaz, stručni
Ključne riječi
Syringocystadenoma papilliferum ; Skin hamartoma ; Child
Sažetak
Objective was to report a very rare case of syringocystadenoma papilliferum, describing its clinical presentation, histopathological appearance and surgical management. An 11-year-old girl presented with a partially lobulated linear plaque on her right lower back present since birth, which was clinically diagnosed at first as linear epidermal nevus. The tumor was surgically removed. The histopathology confirmed the diagnosis of syringocystadenoma papilliferum. Syringocystadenoma papilliferum is a benign adnexal tumor that occurs most often in the head and neck. The tumor has characteristic histological features, and varied and non-distinct clinical findings. Although extremely rare, this lesion should be considered in the differential diagnosis of skin tumors in children.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka
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