CD34/S100 protein–positive, NTRK1-rearranged infantile fibrosarcoma–like tumors in genitourinary system: two cases expanding the clinicopathologic spectrum and illustrating the diagnostic dilemma

Author:

Zhao Ming,Xu Jiayun,Wang Jian

Funder

Ningbo Top Medical and Health Research Program

Project of NINGBO Leading Medical & Health Discipline

Zhejiang Provincial Medicine and Health Research Foundation

Publisher

Springer Science and Business Media LLC

Reference18 articles.

1. Agaram NP, Zhang L, Sung YS, Chen CL, Chung CT, Antonescu CR, Fletcher CD (2016) Recurrent NTRK1 gene fusions define a novel subset of locally aggressive lipofibromatosis-like neural tumors. Am J Surg Pathol 40:1407–1416. https://doi.org/10.1097/PAS.0000000000000675

2. Antonescu CR (2020) Emerging soft tissue tumors with kinase fusions: an overview of the recent literature with an emphasis on diagnostic criteria. Genes Chromosome Cancer 59:437–444. https://doi.org/10.1002/gcc.22846

3. Davis JL, Al-Ibraheemi A, Rudzinski ER, Surrey LF (2020) Mesenchymal neoplasms with NTRK and other kinase gene alterations. Histopathology 80:4–18. https://doi.org/10.1111/his.14443

4. Davis JL, Antonescu C, Bahrami A (2020) Infantile fibrosarcoma. In: WHO Classification of Tumours Editorial Board (eds) WHO classification of tumours of soft tissue and bone, 5th edn. IACR, Lyon, France, pp 119–121

5. Argani P, Calio A, Chang KTE, Cunha IW, de Krijger RR, Vujanic GM (2022) Congenital mesoblastic nephroma. In: WHO Classification of Tumours Editorial Board (eds) WHO classification of urinary and male genital tumours, 5th edn. IACR, Lyon, France, pp 112–113

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