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腱鞘纤维瘤伴 11q 重排。

Fibroma of tendon sheath with 11q rearrangements.

机构信息

Department of Orthopaedic Surgery, Faculty of Medicine, Fukuoka University, Fukuoka, Japan

Department of Pathology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

出版信息

Anticancer Res. 2014 Sep;34(9):5159-62.

Abstract

Fibroma of tendon sheath is an uncommon, benign fibroblastic tumor that usually occurs in the upper extremities of young and middle-aged adults. A clonal chromosomal aberration, t(2;11)(q31-32;q12), has been described in one case. We herein present a unique cytogenetic finding of fibroma of tendon sheath arising in the first web space of the right hand of a 38-year-old woman. Physical examination showed a 3.5-cm, firm, mobile, non-tender mass. Magnetic resonance imaging showed a well-defined soft tissue mass with iso- to slightly-low signal intensity relative to skeletal muscle on both T1- and T2-weighted sequences. Contrast-enhanced T1-weighted sequences demonstrated moderate patchy enhancement of the mass. A fibroma or giant cell tumor of tendon sheath was suggested, and the lesion was marginally excised. Histological examination confirmed the diagnosis of fibroma of tendon sheath. Cytogenetic analysis revealed a novel t(9;11)(p24;q13-14) translocation among other karyotypic abnormalities. The postoperative course was uneventful, and the patient is doing well without local recurrence two months after surgery. To the best of our knowledge, this is only the second report of fibroma of tendon sheath with clonal chromosomal abnormalities.

摘要

腱鞘纤维瘤是一种不常见的良性成纤维细胞瘤,通常发生于中青年上肢。曾有一例报道存在克隆性染色体异常,t(2;11)(q31-32;q12)。我们在此报告一例发生于右手第一掌间隙的腱鞘纤维瘤的独特细胞遗传学发现。患者为 38 岁女性,体格检查发现 3.5cm 大小、质硬、活动度好、无触痛的肿块。磁共振成像(MRI)显示边界清楚的软组织肿块,T1 和 T2 加权序列相对于骨骼肌呈等信号到稍低信号。增强 T1 加权序列显示肿块呈中度斑片状增强。腱鞘纤维瘤或腱鞘巨细胞瘤可能,行边缘性切除。组织学检查证实为腱鞘纤维瘤。细胞遗传学分析显示存在其他染色体异常的新型 t(9;11)(p24;q13-14)易位。术后患者恢复顺利,无局部复发,术后 2 个月随访良好。据我们所知,这是仅有第二例报道的具有克隆性染色体异常的腱鞘纤维瘤。

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