Giant cell fibroblastoma a rare chest wall tumor in a 4 years old boy: a case report

M. Aboud, M. M. Kadhim
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Abstract

Giant cell fibroblastoma (GCF) is an unusual tumor of childhood, primarily occurring in the superficial soft tissues. It is often presented in early childhood as a slowly growing, infiltrative subcutaneous mass at a wide variety of sites. Aim: to present such an interesting rare case of pediatric chest wall lesion. Case report: A 4 years old male patient was admitted to the pediatric surgery unit with complaints of a slow-growing painless palpable, firm swelling in the left chest wall below the left breast. All initial assessments were done, surgery was created. Histopathology and immunohistochemistry revealed the distinctive images of GCF. Conclusion: Although the giant cell fibroblastoma is a rare chest wall tumor in the pediatric age group, it must be considered in differential diagnosis. The histopathology approached has more precise and distinctive images for decision-making regarding the surgery.
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巨细胞成纤维细胞瘤:一罕见的4岁男孩胸壁肿瘤:1例报告
巨细胞成纤维细胞瘤(GCF)是一种罕见的儿童肿瘤,主要发生在浅表软组织。它通常在儿童早期表现为缓慢生长的浸润性皮下肿块,分布于多种部位。目的:报告这样一个有趣的罕见小儿胸壁病变病例。病例报告:一名4岁男性患者因左乳房下方左胸壁有一缓慢生长的无痛性可触及性硬肿而被儿科外科收治。所有的初步评估都完成了,手术开始了。组织病理学和免疫组化显示GCF具有明显的影像特征。结论:虽然巨细胞成纤维细胞瘤在儿童年龄组是一种罕见的胸壁肿瘤,但在鉴别诊断时必须加以考虑。组织病理学方法对手术决策有更精确和独特的图像。
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