Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Syringocystadenoma papilliferum: a rare tumor in an unusual location (CROSBI ID 246397)

Prilog u časopisu | prikaz, osvrt, kritika

Roganović, Jelena ; Brgodac, Ela ; Jonjić, Nives 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

Podaci o odgovornosti

Roganović, Jelena ; Brgodac, Ela ; Jonjić, Nives

engleski

Syringocystadenoma papilliferum: a rare tumor in an unusual location

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.

Syringocystadenoma papilliferum ; Skin hamartoma ; Child

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

11 (1)

2015.

50-53

objavljeno

2490-3671

10.5457/p2005-114.109

Povezanost rada

Kliničke medicinske znanosti

Poveznice