Kao Yu-Chien, Ranucci Valentina, Zhang Lei, Sung Yun-Shao, Athanasian Edward A, Swanson David, Dickson Brendan C, Antonescu Cristina R
*Department of Pathology, Memorial Sloan Kettering Cancer Center §Department of Hand and Upper Extremity Surgery, Hospital for Special Surgery, New York, NY †Department of Pathology, Shuang Ho Hospital, Taipei Medical University, Taipei, Taiwan ‡Division of Anatomic Pathology and Histology, Catholic University, Rome, Italy ∥Department of Pathology, Mount Sinai Hospital, Toronto, ON, Canada.
Am J Surg Pathol. 2017 Nov;41(11):1456-1465. doi: 10.1097/PAS.0000000000000899.
Myxoinflammatory fibroblastic sarcoma (MIFS) is a low grade soft tissue sarcoma with a predilection for acral sites, being associated with a high rate of local recurrence but very infrequent distant metastases. Although a t(1;10) translocation resulting in TGFBR3-MGEA5 fusion has been reported as a recurrent genetic event in MIFS, this abnormality is seen only in a subset of cases. As no studies to date have investigated the spectrum of alternative genetic alterations in TGFBR3-MGEA5 fusion negative MIFS, we undertook a genetic analysis of this particular cohort for further molecular classification. Triggered by an index case occurring in the finger of a 37-year-old female and harboring a novel TOM1L2-BRAF fusion by targeted RNA sequencing we investigated potential recurrent BRAF abnormalities by screening a large group of 19 TGFBR3-MGEA5 fusion negative MIFS by fluorescence in situ hybridization. There were 6 (32%) additional MIFS with BRAF genetic abnormalities, including 5 gene rearrangements and one showing BRAF amplification. Interestingly, VGLL3 amplification, a recurrent genetic abnormality coexisting with t(1;10) in some MIFS, was also detected by fluorescence in situ hybridization in 4/6 (67%) BRAF-rearranged MIFS, but not in the BRAF-amplified case. Up-regulated VGLL3 mRNA expression was also demonstrated in the index case by RNA sequencing. The 7 BRAF-rearranged/amplified MIFS arose in the fingers (n=3), and 1 each in wrist, forearm, foot, and knee, of adult patients (36 to 74 y; M:F=4:3). The histologic spectrum ranged from predominantly solid growth of plump histiocytoid to epithelioid tumor cells with focal myxoid change to a predominantly myxoid background with scattered tumor cells. Varying degree of inflammatory infiltrates and large tumor cells with virocyte-like macronucleoli were observed in most cases. Immunohistochemical stains of phosphorylated ERK, a downstream effector of BRAF activation, were positive in all 4 cases tested (2 diffuse strong, 2 focal strong). Unlike t(1;10), BRAF rearrangements were only found in MIFS but not in 6 hemosiderotic fibrolipomatous tumor (HFLT) lacking TGFBR3-MGEA5 fusions (including 2 pure HFLT, 2 hybrid HFLT-MIFS, and 2 associated with pleomorphic hyalinizing angiectatic tumors).
黏液样炎性成纤维细胞肉瘤(MIFS)是一种低级别软组织肉瘤,好发于肢端部位,局部复发率高,但远处转移很少见。尽管据报道,导致TGFBR3-MGEA5融合的t(1;10)易位是MIFS中反复出现的基因事件,但这种异常仅在一部分病例中出现。由于迄今为止尚无研究调查TGFBR3-MGEA5融合阴性MIFS中其他基因改变的情况,我们对这一特定队列进行了基因分析,以进行进一步的分子分类。由一名37岁女性手指出现的索引病例触发,通过靶向RNA测序发现了一种新的TOM1L2-BRAF融合,我们通过荧光原位杂交对19例TGFBR3-MGEA5融合阴性MIFS的大组病例进行筛查,以研究潜在的复发性BRAF异常。另外有6例(32%)MIFS存在BRAF基因异常,包括5例基因重排和1例BRAF扩增。有趣的是,荧光原位杂交在4/6(67%)BRAF重排的MIFS中也检测到了VGLL3扩增,这是一些MIFS中与t(1;10)共存的反复出现的基因异常,但在BRAF扩增的病例中未检测到。RNA测序在索引病例中也证实了VGLL3 mRNA表达上调。7例BRAF重排/扩增的MIFS发生在成年患者(36至74岁;男:女=4:3)的手指(n=3),以及手腕、前臂、足部和膝盖各1例。组织学谱范围从主要为丰满的组织细胞样到上皮样肿瘤细胞的实性生长,伴有局灶性黏液样改变,到主要为黏液样背景并伴有散在肿瘤细胞。大多数病例观察到不同程度的炎性浸润和带有病毒样大核仁的大肿瘤细胞。BRAF激活的下游效应物磷酸化ERK的免疫组化染色在所有4例检测病例中均为阳性(2例弥漫性强阳性,2例局灶性强阳性)。与t(