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具有非典型特征的肌纤维瘤可酷似低级别肌纤维母细胞肉瘤:两例儿科病例

Myofibroma with Atypical Features can Mimic Low-Grade Myofibroblastic Sarcoma: Two Paediatric Cases.

作者信息

Reyes Magdalena Raquel Torres, Martins Karina Helen, Posantes Gabriela Esperanza Maradiaga, Zelaya Florence Juana Maria Cuadra, Renderos Sandra Guadalupe Góngora, León Jorge Esquiche

机构信息

Department of Pediatric Dentistry, Ribeirão Preto Dental School, University of São Paulo (USP), Ribeirão Preto, Brazil.

Department of Pathology and Diagnosis, School of Dentistry, University of El Salvador, San Salvador, El Salvador.

出版信息

Indian J Otolaryngol Head Neck Surg. 2024 Oct;76(5):4753-4756. doi: 10.1007/s12070-024-04828-z. Epub 2024 Jun 25.

Abstract

Myofibroma is a rare benign mesenchymal tumor that frequently affects the pediatric population with a predilection for the head and neck region. About 10% of myofibroma cases, presenting atypical features, can be misinterpreted as low-grade myofibroblastic sarcoma (LGMS), with therapeutic and prognostic impact. Here, we report two pediatric cases of benign myofibroblastic tumors, one of them showing typical characteristics of myofibroma, the other was an atypical myofibroma, which initially mimicked low-grade myofibroblastic sarcoma. Atypical myofibromas, despite its distinctive characteristics, follow a benign course, similar with typical myofibroma. It is necessary to distinguish atypical myofibroma from low-grade myofibroblastic sarcoma and avoid unnecessary invasive therapy.

摘要

肌纤维瘤是一种罕见的良性间叶组织肿瘤,常发生于儿童,好发于头颈部区域。约10%具有非典型特征的肌纤维瘤病例可能被误诊为低级别肌纤维母细胞肉瘤(LGMS),从而对治疗和预后产生影响。在此,我们报告两例儿童良性肌纤维母细胞肿瘤病例,其中一例具有肌纤维瘤的典型特征,另一例为非典型肌纤维瘤,最初被误诊为低级别肌纤维母细胞肉瘤。非典型肌纤维瘤尽管具有独特特征,但病程呈良性,与典型肌纤维瘤相似。有必要将非典型肌纤维瘤与低级别肌纤维母细胞肉瘤区分开来,避免不必要的侵入性治疗。

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