A Case Report of a Rare Entity - Lateral End of Clavicle Chondromyxoid Fibroma which was Mistaken as Giant Cell Tumor and Aneurysmal Cyst.

N Sharon Rose, Sri Ravindranath Vutukuru, Y Ranjith Kumar, Mettu Anil Kumar, Umesh Sunkari, J H Vidyasagar
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引用次数: 0

Abstract

Introduction: The clavicle is an uncommon site for tumors, as it is a flat bone and rarely affected by neoplasms. Most clavicular tumors are malignant, with metastases and Ewing's sarcoma being the most common. Overall, clavicular neoplasms account for <1% of all bone tumors, and chondromyxoid fibroma (CMF) is particularly rare, comprising <1% of cases. This tumor typically arises in the metaphysis of the proximal tibia.

Case report: A young male patient comes with lateral end clavicle swelling, which on radiologically was diagnosed giant cell tumor. Later on, needle biopsy was thought to be an aneurysmal bone cyst (ABC). Finally, it turned out to be CMF on biopsy.

Conclusion: This case report presents a rare instance in which CMF was initially misdiagnosed as a giant cell tumor based on radiological findings and later as an ABC after histopathological examination. The definitive diagnosis of CMF was only confirmed following excisional biopsy.

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锁骨外侧端软骨粘液样纤维瘤误诊为巨细胞瘤、动脉瘤样囊肿1例。
锁骨是一种不常见的肿瘤部位,因为它是一种平坦的骨,很少受到肿瘤的影响。大多数锁骨肿瘤是恶性的,以转移和尤文氏肉瘤最为常见。总体而言,锁骨肿瘤占病例报告:一名年轻男性患者出现锁骨外侧端肿胀,放射学诊断为巨细胞瘤。后来,针活检被认为是动脉瘤性骨囊肿(ABC)。最后,活检证实为CMF。结论:本病例报告报告了一个罕见的CMF病例,最初根据影像学表现误诊为巨细胞瘤,后来经组织病理学检查误诊为ABC。CMF的明确诊断仅在切除活检后得到证实。
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