prikaz prve stranice dokumenta Syringocystadenoma papilliferum: a rare tumor in an unusual location
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Scientific paper - Case study
Syringocystadenoma papilliferum: a rare tumor in an unusual location
Central European journal of paediatrics, 11 (2015), 1; 50-53. https://doi.org/10.5457/p2005-114.109
Roganović, Jelena; Brgodac, Ela; Jonjić, Nives

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Roganović, J., Brgodac, E. & Jonjić, N. (2015). Syringocystadenoma papilliferum: a rare tumor in an unusual location. Central European journal of paediatrics, 11. (1), 50-53. doi: 10.5457/p2005-114.109

Roganović, Jelena, et al. "Syringocystadenoma papilliferum: a rare tumor in an unusual location." Central European journal of paediatrics, vol. 11, no. 1, 2015, pp. 50-53. https://doi.org/10.5457/p2005-114.109

Roganović, Jelena, Ela Brgodac and Nives Jonjić. "Syringocystadenoma papilliferum: a rare tumor in an unusual location." Central European journal of paediatrics 11, no. 1 (2015): 50-53. https://doi.org/10.5457/p2005-114.109

Roganović, J., Brgodac, E. and Jonjić, N. (2015) 'Syringocystadenoma papilliferum: a rare tumor in an unusual location', Central European journal of paediatrics, 11(1), pp. 50-53. doi: 10.5457/p2005-114.109

Roganović J, Brgodac E, Jonjić N. Syringocystadenoma papilliferum: a rare tumor in an unusual location. Central European journal of paediatrics [Internet]. 2015 [cited 2024 November 14];11(1):50-53. doi: 10.5457/p2005-114.109

J. Roganović, E. Brgodac and N. Jonjić, "Syringocystadenoma papilliferum: a rare tumor in an unusual location", Central European journal of paediatrics, vol. 11, no. 1, pp. 50-53, 2015. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:184:879763. [Accessed: 14 November 2024]

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Metadata
Title (english)Syringocystadenoma papilliferum: a rare tumor in an unusual location
AuthorJelena Roganović
AuthorEla Brgodac
AuthorNives Jonjić
Author's institutionUniversity of Rijeka
Faculty of Medicine
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Pediatrics
Abstract (english)
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.
Keywords (english)
Languageenglish
Publication typeScientific paper - Case study
Publication statusPublished
Peer reviewPeer review - international
Publication versionPublished version
Journal titleCentral European journal of paediatrics
Numberingvol. 11, no. 1, pp. 50-53
e-ISSN2490-3671
DOIhttps://doi.org/10.5457/p2005-114.109
URN:NBNurn:nbn:hr:184:879763
Publication2015
Document URLhttp://bib.irb.hr/916622
Type of resourceText
Access conditionsOpen access
Terms of useLicence Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) icon
Created on2018-12-04 08:02:25