Nodular fasciitis adjacent to the left humerus in a 15-year-old boy

Keita Sasa , Yoshiyuki Suehara , Tatsuya Takagi , Kei Sano , Takuo Hayashi , Tsuyoshi Saito
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Abstract

Nodular fasciitis is often misdiagnosed as its histological mimics, including malignant tumors, due to high levels of cellularity and the presence of occasional mitotic figures. A 15-year-old boy noticed a mass on his left shoulder and was admitted to the hospital. Based on magnetic resonance imaging (MRI) results, the lesion seemed to be located within the muscle, just below the subcutaneous adipose tissue and adjacent to the periosteum of the left humerus. It showed an iso-low signal on T1-weighted images, a heterogeneously high signal on T2-weighted images, and a hyperintense signal on T2 fat-suppression. A fascial tail sign was observed in T2 and T2 fat-suppression sagittal slices. Although the lesion was diagnosed as nodular fasciitis by biopsy, the lesion gradually increased in size up to 3.7 cm during 2 months of follow up after the first admission. The lesion was surgically resected with the marginal margin. Histological analysis showed fascicular proliferation of spindle-shaped cells with inflammatory infiltrates and stromal bleeding. A diagnosis of nodular fasciitis was confirmed by the detection of an MYH-USP6 fusion transcript. The identification of this fusion gene helped to avoid an unnecessary surgical procedure. The patient has been followed up for 6 months after surgery without any evidence of recurrence.

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15岁男孩左肱骨附近结节性筋膜炎
结节性筋膜炎常被误诊为其组织模拟,包括恶性肿瘤,由于高水平的细胞和偶尔存在有丝分裂象。一名15岁的男孩发现自己的左肩有一个肿块,被送进了医院。根据磁共振成像(MRI)结果,病变似乎位于肌肉内,就在皮下脂肪组织下方,毗邻左肱骨骨膜。t1加权呈等低信号,T2加权呈非均匀高信号,T2脂肪抑制呈高信号。T2和T2脂肪抑制矢状面可见筋膜尾征。虽然病变经活检诊断为结节性筋膜炎,但在首次入院后2个月的随访中,病变逐渐增大至3.7 cm。病变手术切除边缘。组织学分析显示纺锤状细胞呈束状增生,伴炎性浸润及间质出血。结节性筋膜炎的诊断通过检测MYH-USP6融合转录物得到证实。这种融合基因的鉴定有助于避免不必要的外科手术。术后随访6个月,无复发迹象。
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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
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0
审稿时长
16 weeks
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