Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient

المؤلفون المشاركون

Harel, Miriam
Makari, John H.

المصدر

Case Reports in Urology

العدد

المجلد 2014، العدد 2014 (31 ديسمبر/كانون الأول 2014)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2014-05-12

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الطب البشري

الملخص EN

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.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Harel, Miriam& Makari, John H.. 2014. Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient. Case Reports in Urology،Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-461805

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Harel, Miriam& Makari, John H.. Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient. Case Reports in Urology No. 2014 (2014), pp.1-4.
https://search.emarefa.net/detail/BIM-461805

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Harel, Miriam& Makari, John H.. Paratesticular Inflammatory Myofibroblastic Tumor in a Pediatric Patient. Case Reports in Urology. 2014. Vol. 2014, no. 2014, pp.1-4.
https://search.emarefa.net/detail/BIM-461805

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-461805