TY  - JOUR
T1  - Paratesticular rhabdomyosarcoma – Spindle cell variant: Case report of a rare tumor
A1  - Akansha Choudhary
A1  - Aswin Veluthattil
A1  - Pooja Mate
JF  - Clinical Cancer Investigation Journal
JO  - Clin Cancer Investig J
SN  - 2278-0513
Y1  - 2018
VL  - 7
IS  - 4
DO  - 10.4103/ccij.ccij_31_18
SP  - 158
EP  - 161
N2  - 
Testicular and paratesticular rhabdomyosarcomas (RMSs) in children are uncommon tumors. Histologically though embryonal RMS is common, the spindle cell variant is considered rare. Paratesticular RMS presents in children and adolescents with a unilateral, painless scrotal swelling or mass above the testis. We report the case of a 15-year-old boy, with a left paratesticular mass who underwent high inguinal orchidectomy. Histopathological examination of the specimen demonstrated spindle cell RMS (SC-RMS). Because of its morphological resemblance to spindle cell neoplasms such as leiomyosarcomas and fibrosarcomas, SC-RMS may pose diagnostic difficulties for the pathologist. This problem can be overcome by a careful search for rhabdomyoblasts in sections and immunohistochemistry for myogenin. We are reporting this case as paratesticular RMS itself is uncommon, and the spindle cell variant of embryonal RMS is all the more rare. There are lacunae in our knowledge about their presentation, diagnosis, response to treatment, and cure.

UR  - https://ccij-online.org/article/paratesticular-rhabdomyosarcoma-–-spindle-cell-variant:-case-report-of-a-rare-tumor-753
ER  -