Mesenchymal Lesion in an Adolescent Girl-A Rare Case Report

Journal Title: Journal of Clinical and Diagnostic Research - Year 2018, Vol 12, Issue 3

Abstract

ABSTRACT Rhabdomyosarcoma (RMS) comprises 3% of all childhood malignancy. Commonly it involves head and neck, extremity and genitourinary systems. Pure primary RMS of breast is a rare malignacy. Here, we present a case of adolescent girl presented with breast lump which was initially treated as benign lesion with excision. Again she presented with recurrent mass which was operated and microscopically showed features of small blue round cell tumour which has lead to many diagnostic confusions both clinically and histopathologically. Immunohistochemistry (IHC) with strong nuclear myogenin positivity in >50% of tumour cells confirms the diagnosis of primary mammary RMS. Postoperative period was uneventful.

Authors and Affiliations

R Manibarathi, AP Rajesh Nataraj, J Pavithra, Bharathi Vidhya Jayanthi

Keywords

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  • EP ID EP502752
  • DOI 10.7860/JCDR/2018/32412.11247
  • Views 86
  • Downloads 0

How To Cite

R Manibarathi, AP Rajesh Nataraj, J Pavithra, Bharathi Vidhya Jayanthi (2018). Mesenchymal Lesion in an Adolescent Girl-A Rare Case Report. Journal of Clinical and Diagnostic Research, 12(3), 3-5. https://www.europub.co.uk/articles/-A-502752