Infantile Inflammatory Myofibroblastic Tumor of Spleen

被引:3
作者
Thirunavukkarasu, Balamurugan [1 ]
Roy, Pritam Singha [2 ]
Gupta, Kirti [1 ]
Sekar, Aravind [1 ]
Bansal, Deepak [2 ]
机构
[1] Post Grad Inst Med Educ & Res, Histopathol, 5th Floor,A Block,Sect 12, Chandigarh 160012, India
[2] Post Grad Inst Med Educ & Res, Pediat, Chandigarh, India
关键词
Inflammatory myofibroblastic tumor; ALK; Epstein– Barr virus; spleen; ROS1; EPSTEIN-BARR-VIRUS; ROS1; ALK; REARRANGEMENTS; PSEUDOTUMOR; EXPRESSION;
D O I
10.1080/15513815.2020.1836098
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Inflammatory myofibroblastic tumor (IMT) is a mesenchymal neoplasm with unknown etiology and recurrent potential. They are widely reported in children and young adults. Nearly 50% of inflammatory myofibroblastic tumor harbor rearrangement in anaplastic lymphoma kinase (ALK) gene with the majority expressing ALK protein. ALK-negative IMTs harbor alteration in ROS1 gene in a subset of cases. Few reports have shown association of IMT with Epstein-Barr virus (EBV). Case report: We report a case of IMT of the spleen in an 18-month-old infant presenting with abdominal distention and failure to thrive. Workup for ALK-1, ROS1, and EBV small-encoded RNA in-situ hybridization using immunohistochemistry was negative. Conclusions: IMT can arise in an infant spleen.
引用
收藏
页码:475 / 479
页数:5
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