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Iranian Journal of Otorhinolaryngology، جلد ۳۱، شماره ۲، صفحات ۱۱۹-۱۲۲
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عنوان فارسی |
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چکیده فارسی مقاله |
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کلیدواژههای فارسی مقاله |
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عنوان انگلیسی |
Giant Congenital Sialolipoma of Parotid Gland with Parapharyngeal Extension |
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چکیده انگلیسی مقاله |
Introduction: Sialolipoma is an extremely rare salivary gland tumor characterized by a well circumscribed mass composed of glandular tissue and mature adipose elements. Herein our aim was to present the fifth case of congenital sialolipoma, which was firstly followed up as a parotid gland hemangioma, and underline the fact that sialolipomas should be kept in mind in the differential diagnosis of congenital parotid gland masses. Case Report: A 10-month old male presented with a left-sided huge neck mass which progressed after birth. Radiologic examination revealed a tumor originating from the parotid gland filling the parapharyngeal space. Histopathologic examination of an incisional biopsy was consistent with sialolipoma. A total parotidectomy with preservation of the facial nerve was performed at the age of 1 year. The postoperative recovery was uneventful with normal facial nerve function. There was no recurrence at the 24-month follow-up. Conclusion: Although it is a very rare benign tumor, congenital sialolipoma should be kept in mind in the differential diagnosis of congenital parotid mass. |
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کلیدواژههای انگلیسی مقاله |
Congenital, Parotid, Sialolipoma |
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نویسندگان مقاله |
| Taner Erdağ Department of Otorhinolaryngology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
| Yüksel Olgun Department of Otorhinolaryngology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
| Melih-Arif Közen Department of Otorhinolaryngology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
| Handan Güleryüz Department of Radiology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
| Erdener Özer Department of Pathology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
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نشانی اینترنتی |
http://ijorl.mums.ac.ir/article_12387.html |
فایل مقاله |
اشکال در دسترسی به فایل - ./files/site1/rds_journals/11/article-11-1290338.pdf |
کد مقاله (doi) |
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زبان مقاله منتشر شده |
en |
موضوعات مقاله منتشر شده |
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نوع مقاله منتشر شده |
Case Report |
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