Syringocystadenoma Papilliferum Revealed 12 Years After Surgical Treatment of Chronic Ear with Cholesteatoma: Presentation of an Unusual Case and Literature Review.

IF 1 4区 医学 Q3 OTORHINOLARYNGOLOGY
Aleksander Zwierz, Krystyna Masna, Paweł Burduk
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引用次数: 0

Abstract

Syringocystadenoma papilliferum is a rare hamartomatous adnexal tumor and appears mainly in the head and neck region. Rarely, such tumors may appear in the external auditory canal. There are only 14 described cases of the syringocystadenoma papilliferum in the external auditory canal in the Medline database. In this study, we present the first reported case of syringocystadenoma papilliferum arising in the modified radical mastoidectomy and occurring 12 years after ear surgery. A 26-year-old man was admitted to our clinic with complaints of discharge from the left ear, ear fullness, and hearing loss. These symptoms had been worsening for 3 years. Twelve years previously, he had undergone modified radical mastoidectomy by Bondy due to a cholesteatoma. Otoscopic examinations revealed otorrhea and a reddish mass measuring 1 × 0.8 cm arising from the tegmen tympanum and fundus of the mastoid cavity. A surgical biopsy was conducted with local anesthesia in the medical outpatient clinic, and it revealed syringocystadenoma papilliferum. A tumor resection was performed with a retroauricular approach. The bone attachment of the tumor was drilled out, and the ear cavity was covered with a mashed split skin graft. The ear cavity healed, and no tumor recurrence was observed during a 9-month follow-up period. Our case and literature analysis of previously described cases led to the conclusion that cases of syringocystadenoma papilliferum of the external auditory canal may be associated with different medical histories, age distributions, and origins than other syringocystadenoma papilliferums of the head and neck region. Tubular adenoma may occur together with syringocystadenoma papilliferum in 20% of cases. Malignant transformation of syringocystadenoma papilliferum may occur but is extremely rare. Computed tomography imaging may predict malignancy of the tumor. Tumors specific to the external auditory canal may occur in the modified radical mastoidectomy after middle ear surgery.

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慢性耳部胆脂瘤手术治疗12年后发现乳头状淋巴管囊腺瘤:一例罕见病例的报告及文献复习。
摘要乳头状淋巴管囊腺瘤是一种罕见的错构瘤性附件肿瘤,主要发生于头颈部。这种肿瘤很少出现在外耳道。在Medline数据库中,只有14例外耳道的脊髓囊腺瘤乳头状瘤。在这项研究中,我们报告了第一例在改良根治性乳突切除术中出现的乳头状囊腺瘤,发生在耳部手术12年后。一名26岁男子因左耳分泌物、耳胀及听力丧失而入院。这些症状已经恶化了3年。12年前,由于胆脂瘤,他接受了Bondy的改良根治性乳突切除术。耳镜检查发现耳漏和1 × 0.8 cm的红色肿块,位于鼓膜和乳突腔底部。门诊在局部麻醉下行手术活检,结果显示为脊髓囊腺瘤乳头状瘤。经耳后入路行肿瘤切除术。将肿瘤的骨附着体钻出,耳腔覆盖碎皮移植片。随访9个月,耳腔愈合,无肿瘤复发。我们对先前病例的病例和文献分析得出结论,外耳道乳头状囊腺瘤病例可能与头颈部其他乳头状囊腺瘤病例具有不同的病史、年龄分布和起源。在20%的病例中,管状腺瘤可能与乳头状囊状腺瘤同时发生。乳头状淋巴管囊腺瘤可能发生恶性转化,但极为罕见。计算机断层成像可以预测肿瘤的恶性。中耳手术后改良乳突根治术可发生外耳道特异性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
94
审稿时长
6-12 weeks
期刊介绍: The Journal of International Advanced Otology (IAO – Citation Abbreviation: J Int Adv Otol) is an open access double-blind peer-reviewed, international publication. The Journal of International Advanced Otology is fully sponsored and owned by the European Academy of Otology and Neurotology and the Politzer Society. The Journal of International Advanced Otology is published 3 times per year on April, August, December and its publication language is English. The scope of the Journal is limited with otology, neurotology, audiology (excluding linguistics) and skull base medicine. The Journal of International Advanced Otology aims to publish manuscripts at the highest clinical and scientific level. IAO publishes original articles in the form of clinical and basic research, review articles, short reports and a limited number of case reports. Controversial patient discussions, communications on emerging technology, and historical issues will also be considered for publication.
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