[Drug-resistant genito-urinary rhabdomyosarcoma in children with primary psoas abscess. Apropos of a case].

Journal d'urologie Pub Date : 1997-01-01
T Merrot, V Moutardier, P Viens, F Bladou, J R Delpero
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Abstract

We report an unusually uncommon case of genitourinary rhabdomyosarcoma in a child which was chemoresistant and complicated by a primary psoas abscess which presented as a pelvic mass associated with an abscess of the right iliac fossa. Ultrasound and CT investigations suggested the diagnosis of a centropelvic tumor which was confirmed at puncture-aspiration. MRI was most contributive giving a precise description of the local extension. Intensive multi-drug chemotherapy would appear to have improved outcome in patients with poor-prognosis Maurer group III tumors. In exceptional cases when no tumor response is obtained, carcinological surgery with large dissection, possibly with adjuvant radiotherapy, is indicated. Percutaneous drainage of the deep psoas abscess is as effective as classical surgery and spares the abdominal wall, particularly important if a second operation should be needed. Multidisciplinary management is required for the treatment of this highly malignant tumor.

原发性腰肌脓肿患儿的耐药泌尿生殖横纹肌肉瘤。关于一个案例]。
我们报告一个不寻常的病例泌尿生殖系统横纹肌肉瘤的儿童,这是化疗耐药和并发原发性腰肌脓肿,表现为盆腔肿块与脓肿的右侧髂窝。超声及CT检查提示盆腔中心肿瘤,经穿刺穿刺确认。MRI最有助于精确描述局部延伸。强化多药化疗似乎可以改善预后不良的Maurer III组肿瘤患者的预后。在没有肿瘤反应的特殊情况下,需要进行肿瘤手术并进行大剥离,可能还需要辅助放疗。经皮腰深脓肿引流术与传统手术一样有效,且不伤及腹壁,尤其在需要二次手术时尤为重要。这种高度恶性肿瘤的治疗需要多学科的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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