Rhabdomyosarcoma arising from retroperitoneal teratoma in an infantile neurofibromatosis type 1 patient. Issue 8 (21st July 2019)

• Record Type: Journal Article
• Authors: Aikawa, Akane; Mizutani, Kenichi; Futatsuya, Chizuru; Kumagai, Motona; Shioya, Akihiro; Nakada, Satoko; Kurose, Nozomu; Nojima, Takayuki; Tsuzuki, Toyonori; Yamada, Sohsuke
• Is Part Of: Pathology international. Volume 69:Issue 8(2019)
• Page Start: 488
• Page End: 495
• Publication Date: 2019-07-21
• Subjects: electron microscope -- Isochromosome 12p -- neurofibromatosis 1 -- pediatric -- retroperitoncal -- rhabdomyosarcoma; Pathology -- Periodicals; 616.07
• DOI: 10.1111/pin.12810
• Languages: English
• ISSNs: 1320-5463

Abstract

Abstract : We herein report the case of a 2‐year‐old girl with neurofibromatosis type 1 (NF1), who presented with a 12‐cm mass in the right retroperitoneum and underwent tumor resection. Histologically, the tumor was composed of two distinct components: one was teratoma, showing mature morphology; and the other was embryonal rhabdomyosarcoma. An interphase fluorescence in situ hybridization (FISH) analysis of the rhabdomyosarcoma component revealed the absence of isochromosome 12p. Although it is well known that rhabdomyosarcoma occurs in infantile NF1, and that rhabdomyosarcoma can arise from teratoma as a somatic‐type malignancy, to the best of our knowledge, this is the first case of an infantile NF1 patient, who developed rhabdomyosarcoma within a retroperitoneal teratoma. The absence of chromosome 12p alteration suggests a possibility that the rhabdomyosarcoma occurred due to the NF1 background, not as a somatic‐type malignancy of germ cell tumor.