Paratesticular rhabdomyoma is a rare benign tumor, which usually presents as a painless mass in the scrotum or groin. We report the first case of a locally invasive paratesticular rhabdomyoma in a 17-year-old male teenager who presented with chronic scrotal pain. We further review the current literature of this rare tumor.
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Molecular assessment of paratesticular rhabdomyomas demonstrates recurrent findings, including a novel H3C2 p.K37I mutation.
Mod Pathol
December 2022
Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.
Rhabdomyomas are benign tumors with skeletal muscle differentiation that are broadly divided into cardiac and extracardiac types. The latter demonstrate a predilection for head and neck and genital locations and are further subclassified into adult-type rhabdomyoma (ATRM), fetal-type rhabdomyoma (FTRM) and genital rhabdomyoma (GRM). Most extracardiac rhabdomyomas that arise in paratesticular tissues have a somewhat distinctive morphology and have been termed sclerosing rhabdomyomas (SRM).
View Article and Find Full Text PDFParatesticular rhabdomyoma: a morphologically distinct sclerosing variant.
Am J Surg Pathol
November 2013
*Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA †Department of Pathology, University of Florida College of Medicine, Gainesville, FL ‡Department of Pathology, Institut Bergonie, Bordeaux, France.
Extracardiac rhabdomyomas, which currently are classified into fetal, adult, and genital types, are rare. We have identified 7 cases of a distinct morphologic variant of rhabdomyoma that affects mainly young men in the paratesticular region, seen in consultation between 2001 and 2011. The 7 male patients were adults (median age 24 y) and presented with tumors in paratesticular soft tissue (4 left-sided, 3 right-sided).
View Article and Find Full Text PDFParatesticular fetal-type rhabdomyoma in a 12-year-old boy: a case report and literature review.
Urology
November 2013
Department of Dermatology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, China.
Fetal rhabdomyoma (F-RM) is a very rare tumor that usually occurs in the head and neck. Paratesticular F-RM in children is extremely rare. In this article, we report the case of a 12-year-old boy diagnosed with paratesticular F-RM.
View Article and Find Full Text PDFParatesticular rhabdomyoma in a young adult: case study and review of the literature.
J Pediatr Surg
April 2007
Division of Pediatric Urology, Children's Hospital of Pittsburgh, Pittsburgh, PA 15213, USA.
Paratesticular rhabdomyoma is a rare benign tumor, which usually presents as a painless mass in the scrotum or groin. We report the first case of a locally invasive paratesticular rhabdomyoma in a 17-year-old male teenager who presented with chronic scrotal pain. We further review the current literature of this rare tumor.
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