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先天性颗粒细胞瘤伴不常见临床表现。

Congenital granular cell tumor with uncommon clinical behavior.

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, General Hospital Salzburg, University Hospital of Paracelsus Medical University, Salzburg, Austria.

出版信息

Laryngoscope. 2013 Oct;123(10):2459-62. doi: 10.1002/lary.23919. Epub 2013 Aug 5.

Abstract

Congenital granular cell tumor (CGCT), also known as congenital epulis, is a rare benign mesenchymal tumor of the oral cavity. We report of a 3 years and 7 months old female patient undergoing surgical excision of an oral tumor. Subsequent histological and immunohistological investigations within the clinical course led to the diagnosis of CGCT. However, clinical findings in this case, such as primary onset and an untypical location within the oral cavity, clearly stand in contrast to those usually found in CGCT, resulting in an exceptional case not previously described in the literature.

摘要

先天性颗粒细胞瘤(CGCT),又称先天性龈瘤,是一种罕见的口腔良性间叶组织肿瘤。我们报告了一例 3 岁零 7 个月的女性患者,行口腔肿瘤切除术。在临床过程中进行的后续组织学和免疫组织化学研究导致了 CGCT 的诊断。然而,在这种情况下的临床发现,如原发性和口腔内不典型位置,与 CGCT 通常发现的情况明显不同,导致了一个以前在文献中未描述的特殊病例。

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