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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Format: | Article |
Language: | English |
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Wiley
2014-01-01
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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. |
format | Article |
id | doaj-art-eecaf23eec5a474a9ba4116547b50d70 |
institution | Kabale University |
issn | 2090-696X 2090-6978 |
language | English |
publishDate | 2014-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Urology |
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 |