小儿口面部结节性筋膜炎:罕见病例报告及文献复习。

IF 0.7 Q4 SURGERY
Maryam Salah, Mouna Rimani, Laïla Benjelloun, Bouchra Taleb
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引用次数: 0

摘要

结节性筋膜炎是一种罕见的、良性的、快速生长的、自限性的肌纤维母细胞/纤维母细胞假肿瘤,通常与肉瘤相似,因此其诊断特别具有挑战性。虽然它通常发生在躯干和四肢的皮下组织,但口腔内的表现非常罕见。病例介绍:我们报告一例罕见的口腔结节性筋膜炎病例,患者为10岁,表现为右下前磨牙延迟出疹,相应区域出现坚固、迅速增大、无痛性肿胀。切除活检后进行免疫组织化学分析,证实结节性筋膜炎的诊断。临床讨论:结节性筋膜炎的临床及病理与恶性病变相似,极易误诊,导致过度治疗。认识到它的主要特点是必不可少的,以避免不必要的和侵入性的程序,特别是在儿科患者。结论:本病例强调了在快速增长的口腔软组织肿块鉴别诊断中考虑结节性筋膜炎的重要性,特别是在儿童中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pediatric nodular fasciitis of the orofacial region: A rare case report and literature review.

Introduction: Nodular fasciitis is a rare, benign, rapidly growing, self-limited myofibroblastic/fibroblastic pseudotumor that often mimics sarcomas, making its diagnosis particularly challenging. While it typically occurs in the subcutaneous tissues of the trunk and extremities, intraoral presentation is extremely uncommon.

Case presentation: We report a rare case of oral nodular fasciitis in a 10-year-old patient who presented with delayed eruption of the right lower premolars and a firm, rapidly enlarging, painless swelling in the corresponding region. An excisional biopsy was performed, followed by immunohistochemical analysis, which confirmed the diagnosis of nodular fasciitis.

Clinical discussion: Due to its clinical and histopathological resemblance to malignant lesions, nodular fasciitis can easily be misdiagnosed, potentially leading to overtreatment. Recognizing its key features is essential to avoid unnecessary and invasive procedures, especially in pediatric patients.

Conclusion: This case highlights the importance of considering nodular fasciitis in the differential diagnosis of rapidly growing soft tissue masses in the oral cavity, particularly in children.

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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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