Publication:
Syringocystadenoma Papilliferum in the External Ear Canal

dc.contributor.authorJakovljevic, Sasa (57455265100)
dc.contributor.authorArsovic, Nenad (17033449500)
dc.contributor.authorBoricic, Novica (56515320500)
dc.contributor.authorLaketic, Darko (25936376800)
dc.contributor.authorDudvarski, Zoran (6504165244)
dc.date.accessioned2025-06-12T12:36:38Z
dc.date.available2025-06-12T12:36:38Z
dc.date.issued2022
dc.description.abstractOut of all benign tumors of the ceruminous glands, syringocystadenoma papilliferum is the rarest and represents only 2% of cases. It is an extremely rare benign tumor that originates from modified apocrine sweat glands. The aim of this paper was to present, according to our findings, the 18th case of syringocystadenoma papilliferum in the external auditory canal, with a detailed review of its clinical, radiological and histomorphological characteristics. A 59-year-old man reported to our clinic due to a 5 × 5 mm papillomatous growth at the entrance to the right external auditory canal. Histopathology indicated, after an excisional biopsy, that it was a syringocystadenoma papilliferum. The resection lines were free of tumor tissue, and the patient has no signs of tumor recurrence. Although rare, it should be considered as a differential diagnosis of lesions in this region. Complete excision is mandatory in order to avoid recurrence and potential malignant alteration. © 2022 Academy of Medical Sciences of I.R. Iran. All rights reserved.
dc.identifier.urihttps://doi.org/10.34172/aim.2022.101
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85144927703&doi=10.34172%2faim.2022.101&partnerID=40&md5=54a2f12fa2669457c310dbc670e9d2e4
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/3257
dc.subjectCeruminous gland
dc.subjectExternal auditory canal
dc.subjectSyringocystadenoma papilliferum
dc.titleSyringocystadenoma Papilliferum in the External Ear Canal
dspace.entity.typePublication

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