Multidisciplinary approach is needed for the management and disease localized to the scrotum has a favorable outcome
📌 3 Maddede Bu Makale
🎯
Amaç & Hipotez:Extremities are the usual site of involvement in Rhabdomyosarcomas whereas paratesticular rhabdomyosarcoma is an extremely rare, which is known to be an aggressive variety of paratesticular tumors occurring in first and second decades of life.
📊
Temel Bulgular & Veri:They usually develop from the tunica, epididymis or the spermatic cord.
💡
Sonuç & Katkı:Multidisciplinary approach is needed for the management and disease localized to the scrotum has a favorable outcome
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri
Abstract
Extremities are the usual site of involvement in Rhabdomyosarcomas whereas paratesticular rhabdomyosarcoma is an extremely rare, which is known to be an aggressive variety of paratesticular tumors occurring in first and second decades of life. They usually develop from the tunica, epididymis or the spermatic cord. Precise preoperative diagnosis is seldom established. It can be mistaken as epididymitis, scrotal abscess, hydrocele, testicular tumors, tuberculosis of testis and strangulated or obstructed inguinal hernia, as in our case. Multidisciplinary approach is needed for the management and disease localized to the scrotum has a favorable outcome
🔖
Bu Makaleye Atıf Yap
SHUKLA, A., BHARTİ, R., SHARMA, S., CHAUDHRY, R., VERMA, V. (2015). Rare case of paratesticular rhabdomyosarcoma. Pediatric Urology Case Reports, Cilt: 2 - Sayı: 6, 9–14. https://ajindex.com/articles/285679
Stewart LH, Lioe TF, Johnston SR. Thirty-year review of intrascrotal rhabdomyosarcoma. Br J Urol. 1991;68(4):418-20.
Jaffe N, Filler RM, Farber S, Traggis DG, Vawter GF, Tefft M, et al. Rhabdomyosarcoma in children. Improved outlook with a multidisciplinary approach. Am J Surg. 1973;125(4):482- 7. Khoubehi B, Mishra V, Ali M, Motiwala H, Karim O. Adult paratesticular tumours. BJU International. 2002;90(7):707-15.
McCarville MB, Spunt SL, Pappo AS. Rhabdomyosarcoma in pediatric patients: the good, the bad, and the unusual. AJR Am J Roentgenol. 2001;176(6):1563-9.
Trippitelli A, Rosi P, Selli C, Carini M, Turini D. Rhabdomyosarcoma of spermatic cord in adult. Urology. 1982;19(5):533-5.
Ali SZ, Smilari TF, Teichberg S, Hajdu SI. Pleomorphic rhabdomyosarcoma of the heart metastatic to bone. Report of a case with fine needle aspiration biopsy findings. Acta Cytol. 1995;39(3):555-8.
Ferrari A, Bisogno G, Casanova M, et al. Paratesticular rhabdomyosarcoma: report from the Italian and German Cooperative Group. J Clin Oncol. 2002;20(2):449-55.
Mak CW, Chou CK, Su CC, Huan SK, Chang JM. Ultrasound diagnosis of paratesticular rhabdomyosarcoma. Br J Radiol. 2004;77(915):250-2.
Lawrence W Jr, Hays DM, Heyn R, et. Lymphatic metastases with childhood rhabdomyosarcoma. A report from the Intergroup Rhabdomyosarcoma Study. Cancer. 1987;60(4):910-5.
Boulma R, Gargouri MM, Sallemi A, et al. Paratesticular pleomorphic rhabdomyosarcoma: A report of two cases. Case Rep Urol. 2013; 2013:807979. Stewart RJ, Martelli H, Oberlin O, Rey A, Bouvet N, Spicer RD, et al. Treatment of children with nonmetastatic paratesticular rhabdomyosarcoma: Results of the malignant mesenchymal tumors studies Okur et al / Ped Urol Case Rep 2015;2(6):15-19 (MMT 84 and MMT 89) of the International Society of Pediatric Oncology. J Clin Oncol. 2003;21(5):793-8.
Kumar R, Bharti S, Khosla D, Kapoor R. Long term survival in paratesticular rhabdomyosarcoma. Clin Cancer Investig J. 2012;1(1):31-2. Access this article online http://pediatricurologycasereports.com Quick Response Code