Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient

Although rare, paratesticular inflammatory myofibroblastic tumor (IMT) represents the second most common paratesticular mass after adenomatoid tumor and comprises roughly 6% of such lesions. Only approximately four cases have been reported in patients younger than 18 years of age. We report an incid...

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Main Authors: Miriam Harel, John H. Makari
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Case Reports in Urology
Online Access:http://dx.doi.org/10.1155/2014/303678
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author Miriam Harel
John H. Makari
author_facet Miriam Harel
John H. Makari
author_sort Miriam Harel
collection DOAJ
description Although rare, paratesticular inflammatory myofibroblastic tumor (IMT) represents the second most common paratesticular mass after adenomatoid tumor and comprises roughly 6% of such lesions. Only approximately four cases have been reported in patients younger than 18 years of age. We report an incidentally discovered paratesticular IMT in a 17-year-old male successfully treated with wide excision and testis sparing. To our knowledge, no recurrence has been reported after complete excision of paratesticular IMT; however, continued follow-up is recommended.
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spelling doaj-art-eecaf23eec5a474a9ba4116547b50d702025-02-03T06:44:48ZengWileyCase Reports in Urology2090-696X2090-69782014-01-01201410.1155/2014/303678303678Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric PatientMiriam Harel0John H. Makari1University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030, USAUniversity of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030, USAAlthough rare, paratesticular inflammatory myofibroblastic tumor (IMT) represents the second most common paratesticular mass after adenomatoid tumor and comprises roughly 6% of such lesions. Only approximately four cases have been reported in patients younger than 18 years of age. We report an incidentally discovered paratesticular IMT in a 17-year-old male successfully treated with wide excision and testis sparing. To our knowledge, no recurrence has been reported after complete excision of paratesticular IMT; however, continued follow-up is recommended.http://dx.doi.org/10.1155/2014/303678
spellingShingle Miriam Harel
John H. Makari
Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient
Case Reports in Urology
title Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient
title_full Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient
title_fullStr Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient
title_full_unstemmed Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient
title_short Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient
title_sort paratesticular inflammatory myofibroblastic tumor in a pediatric patient
url http://dx.doi.org/10.1155/2014/303678
work_keys_str_mv AT miriamharel paratesticularinflammatorymyofibroblastictumorinapediatricpatient
AT johnhmakari paratesticularinflammatorymyofibroblastictumorinapediatricpatient