儿童硬腭涎脂瘤：一例罕见病例及文献复习
Sialolipoma of the Hard Palate in a Child: An Unusual Case and Review of the Literature.
作者信息
Yesilyurt Mustafa, Polat Gökhan, Pirimoglu Berhan, Sade Recep, Gundogdu Betul
机构信息
Department of Radiology, Medical Faculty, Ataturk University, Erzurum, Turkey.
Department of Radiology, Faculty of Medicine, Ataturk University, Erzurum, 25040 Turkey.
出版信息
Indian J Otolaryngol Head Neck Surg. 2025 Feb;77(2):1037-1040. doi: 10.1007/s12070-024-05270-x. Epub 2024 Dec 5.
Abstract
Sialolipoma is a benign lipomatous tumor that occurs in the salivary glands. Sialolipoma of the minor salivary gland is also uncommon in the pediatric population. Here, we present the first reported case of hard palate sialolipoma in a 4-year-old girl.
摘要
涎腺脂肪瘤是一种发生于涎腺的良性脂肪瘤性肿瘤。小涎腺涎腺脂肪瘤在儿童群体中也不常见。在此，我们报告首例4岁女童硬腭涎腺脂肪瘤病例。
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本文引用的文献
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Sialolipoma of infancy - a rare benign salivary gland neoplasm and a potential diagnostic pitfall in cytology.婴儿期涎腺脂肪瘤——一种罕见的良性涎腺肿瘤，也是细胞学诊断中的一个潜在陷阱。
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Congenital sialolipoma of parotid gland: a report of rare and recently described entity with review of literature.腮腺先天性涎脂瘤：一种罕见且近期才被描述的实体病例报告并文献复习
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Sialolipoma of the parotid gland with diffuse sebaceous differentiation in a female child.一名女童腮腺的涎脂瘤伴弥漫性皮脂腺分化。
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10
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Int J Pediatr Otorhinolaryngol. 2005 Mar;69(3):429-34. doi: 10.1016/j.ijporl.2004.10.014. Epub 2004 Dec 15.
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