Infantile Myofibroma of the Frontal Bone: A Case Report

FACE Pub Date : 2024-03-27 DOI:10.1177/27325016241241782
K. A. Alawi, Ruqaya Al Abri, S. A. Shaqsi, Jehad Al Habsi, Ahmed Al Azri, Taimoor Al Balushi
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Abstract

Infantile myofibroma stands as the most prevalent fibrous neoplasm within the pediatric population, despite its rarity. The majority of these tumors manifest within the initial 2 years of life. Clinically, myofibroma lesions are classified into solitary and multicentric tumors. We present a case of infantile myofibroma located within the frontal bone of a 16-month-old infant. Initial evaluation of the swelling and its spread was conducted using CT and MRI scans. Subsequently, the diagnosis was confirmed through a core needle biopsy. The tumor underwent surgical excision with 1 cm safety margin and immediate reconstruction with strips of calvaria bone graft. Histopathology of the specimen showed complete tumor clearance with actual margin of 7 mm. The surgical resection of cranial benign bone tumors should be meticulously planned with a multidisciplinary approach. Wherever possible, immediate reconstruction should be conducted to avoid the morbidity of a subsequent procedure.
婴儿额骨肌纤维瘤:病例报告
婴幼儿肌纤维瘤虽然罕见,但却是儿科最常见的纤维性肿瘤。这些肿瘤大多在婴儿出生后的最初两年内发病。临床上,肌纤维瘤可分为单发性和多中心性两种。我们介绍了一例位于16个月大婴儿额骨内的婴儿肌纤维瘤。通过 CT 和 MRI 扫描对肿物及其扩散情况进行了初步评估。随后,通过核心针刺活检确诊。手术切除了肿瘤,留出了 1 厘米的安全边缘,并立即进行了腓骨移植重建。标本的组织病理学检查显示肿瘤完全清除,实际边缘为 7 毫米。颅骨良性骨肿瘤的手术切除应通过多学科方法精心策划。在可能的情况下,应立即进行重建,以避免后续手术的发病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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