Literature DB >> 27182845

Primary Renal Rhabdomyosarcoma: An Unusual Bone Metastasizing Tumor of Kidney.

Shabnam Parvin1, Ranajoy Ghosh1, Ram Narayan Das1, Koushik Saha2, Paromita Roy3, Chhanda Datta1, Uttara Chatterjee1.   

Abstract

Rhabdomyosarcoma (RMS) is one of the common malignant tumors in the pediatric age group. There is only a single case report of primary renal alveolar RMS. Fine needle aspiration (FNA) findings of primary renal RMS has not been reported so far. Hence we present an unusual case of primary alveolar RMS of the kidney. An 11 year old boy presented with an abdominal mass. On FNA a diagnosis of undifferentiated sarcoma and anaplastic Wilms tumor were considered. The tumor was resected and showed histopathological features of alveolar rhabdomyosarcoma. He developed multiple bony metastases and succumbed to the illness despite aggressive chemotherapy. RMS of the kidney should be considered in the differential diagnosis of children with a renal mass, and may have an aggressive clinical course with bone metastases.

Entities:  

Keywords:  Renal neoplasm; rhabdomyosarcoma; undifferentiated sarcoma

Mesh:

Substances:

Year:  2016        PMID: 27182845     DOI: 10.1080/15513815.2016.1175528

Source DB:  PubMed          Journal:  Fetal Pediatr Pathol        ISSN: 1551-3815            Impact factor:   0.958


  1 in total

1.  Primary Renal Ewing Sarcoma in Children and Young Adults.

Authors:  Kathryn Bradford; Alexander Nobori; Brittany Johnson; Wendy Allen-Rhoades; Bindi Naik-Mathuria; Eduard H Panosyan; Moran Gotesman; Joseph Lasky; Jerry Cheng; Alan Ikeda; Jeffrey Goldstein; Arun Singh; Noah Federman
Journal:  J Pediatr Hematol Oncol       Date:  2020-11       Impact factor: 1.170

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.