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A Rare Tumor of the Scalp: Papilliferous Cystadenoma

A Rare Tumor of the Scalp: Papilliferous Cystadenoma

作     者:Alexis do Santos Zounon Bidossessi Ulrich Vodouhe Wilfrid Akpo Sonia Lawson Afouda François Avakoudjo Wassi Adjibabi Alexis do Santos Zounon;Bidossessi Ulrich Vodouhe;Wilfrid Akpo;Sonia Lawson Afouda;François Avakoudjo;Wassi Adjibabi

作者机构:Faculty of Health Sciences Abomey-Calavi University Abomey Calavi Bénin 

出 版 物:《International Journal of Otolaryngology and Head & Neck Surgery》 (耳鼻喉(英文))

年 卷 期:2023年第12卷第6期

页      面:390-396页

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

主  题:Scalp Tumor Papilliferous Cystadenoma 

摘      要:Introduction: Papilliferous cystadenoma is a rare adnexal tumor of early childhood. Case Report: We report a case of papilliferous cystadenoma of the scalp in a 22-year-old adult with no previous history of the disease. She had been presenting with a slowly progressing scalp mass for about 10 years. The mass was mildly pruritic and painless, but the patient reported several painful episodes treated with local herbal applications and unspecified antibiotics. On inspection, the lesion was raised, granular, sessile and vegetated, greyish in color, with an irregular surface, nippled and hemispherical in shape. On palpation, the lesion was painless, fleshy and surrounded by crusts that were easily removed by applying a saline-moistened compress. The patient underwent excision with at least 4-mm margins. Pathological examination of the operative specimen revealed a papilliferous syringocystadenoma. There was no tumor recurrence after three years. Conclusion: Papilliferous cystadenoma is a rare benign tumor of the scalp requiring clinical analysis and surgical excision to confirm its histological nature. Post-operative follow-up is necessary due to frequent recurrences.

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