小儿前臂肌纤维瘤病1例报告并文献复习

Q4 Medicine
Asmae Guennouni, Zineb Labbi, Chaimae Abourak, Soukaina Bahha, Siham El Haddad, Nazik Allali, Latifa Chat
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引用次数: 0

摘要

本病例是一名 15 岁的女孩,无明显病史,3 年来前臂出现逐渐增大的无痛性肿胀。影像学检查发现她的前臂有一个带有 "旭日 "骨膜反应的溶解性病变,组织学分析证实了她患有婴儿肌纤维瘤病。尽管患者接受了长春新碱和甲氨蝶呤化疗,但病情未见好转,曾考虑过包括截肢在内的手术治疗方案,但被患者拒绝。本病例突出了影像学在诊断和评估肌纤维瘤病程度方面的重要性,同时强调了个性化治疗方法的必要性,以及对晚期或无法手术病例的有效疗法的进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Infantile myofibromatosis of the forearm: A case report and literature review
We present the case of a 15-year-old girl with no significant medical history who developed a progressively enlarging, painless swelling in her forearm over a period of 3 years. Imaging revealed a lytic lesion with a “sunburst” periosteal reaction, and histological analysis confirmed the diagnosis of infantile myofibromatosis. Despite chemotherapy with Vinblastine and Methotrexate, no improvement was observed, and surgical options, including amputation, were considered but declined by the patient. This case highlights the importance of imaging in diagnosing and evaluating the extent of myofibromatosis, while emphasizing the need for personalized treatment approaches and further research into effective therapies for advanced or inoperable cases.
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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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