Chondromyxoid Fibroma of the Temporal Bone: Case Report and Literature Review

IF 0.1 Q4 PATHOLOGY AJSP: reviews & reports Pub Date : 2021-01-01 DOI:10.1097/PCR.0000000000000421
A. Grover, R. Mannem, Bryan C. Hunt, Reena Singh
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Abstract

Abstract Chondromyxoid fibroma (CMF) is a rare, benign, cartilaginous bone tumor that commonly affects the metaphysis of the lower-extremity long bones in young adults. Involvement of the craniofacial bones, especially the temporal bone, is exceedingly rare. We report a case of a 64-year-old man who presented with a left ear mass, but on subsequent imaging was found to have a more extensive mass centered in the temporal bone. Initial biopsy raised the concern for a low-grade chondrosarcoma. However, following surgical resection, a diagnosis of CMF was rendered. The clinical findings, radiographic features, histology, and differential diagnoses are discussed.
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颞骨软骨粘液样纤维瘤:病例报告及文献复习
软骨粘液样纤维瘤(CMF)是一种罕见的良性软骨骨肿瘤,常见于年轻人下肢长骨干骺端。累及颅面骨,尤其是颞骨,是非常罕见的。我们报告一个64岁男性的病例,他表现为左耳肿块,但随后的影像学发现有一个更广泛的肿块,以颞骨为中心。最初的活检提示为低级别软骨肉瘤。然而,手术切除后,诊断为CMF。临床表现,影像学特征,组织学和鉴别诊断进行了讨论。
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