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睾丸旁促纤维增生性小圆细胞肿瘤:病例报告

Paratesticular desmoplastic small round cell tumor: case report.

作者信息

García-González Jesús, Villanueva Concepción, Fernández-Aceñero M Jesús, Paniagua Pedro

机构信息

Department of Urology, Hospital General of Móstoles, Madrid, Spain.

出版信息

Urol Oncol. 2005 Mar-Apr;23(2):132-4. doi: 10.1016/j.urolonc.2004.09.009.

Abstract

BACKGROUND

The desmoplastic small round cell tumor has recently been separated from other small round cell tumors because of its characteristic pathological and clinical features. They are usually intra-abdominal tumors affecting young people and have classically been associated with a bad prognosis. However, in recent years there have reports on desmoplastic small round cell tumors affecting other body regions, including the paratesticular area.

CASE PRESENTATION

We report the case of a 23-year-old male, that consulted on a progressive enlargement of the right hemiscrotum in the last year and a half. He referred no previous urological symptoms and had no systemic symptomatology. Physical examination revealed a round elastic firm 2 to 3 cm mass distal to the tail of the epididymis, which was excised with a preoperative diagnosis of adenomatoid tumor. However, histological and immunohistochemical diagnosis confirmed a desmoplastic small round cell tumor. The extension study included a computed tomography scan and a plain chest radiograph, that showed no metastasis. The patient received chemoradiation therapy with methotrexate, dacarbacin, cyclophosphamide, actinomycin D and vincristin, but had to be changed to a vincristin, actinomycin D, cyclophosphamide and adriamicin scheme on severe toxicity. He completed five cycles of the chemotherapy with moderate toxicity. Today, 6 years after diagnosis the patient remains well and free of disease.

CONCLUSIONS

Recent reviews on desmoplastic small round cell tumor affecting the paratesticular area have shown a better prognosis for tumors of this origin compared to abdominal ones. We should include this lesion among the differential diagnosis of paratesticular tumors, mainly in children and adolescents.

摘要

背景

促纤维增生性小圆细胞瘤因其独特的病理和临床特征,最近已从其他小圆细胞瘤中分离出来。它们通常是发生于年轻人的腹腔内肿瘤,传统上预后较差。然而,近年来有报道称促纤维增生性小圆细胞瘤可发生于身体的其他部位,包括睾丸旁区域。

病例报告

我们报告一例23岁男性患者,在过去一年半中因右侧阴囊渐进性肿大前来就诊。他既往无泌尿系统症状,也无全身症状。体格检查发现附睾尾部远端有一个2至3厘米大小的圆形、质地坚韧且有弹性的肿块,术前诊断为腺瘤样瘤并行切除。然而,组织学和免疫组化诊断证实为促纤维增生性小圆细胞瘤。进一步检查包括计算机断层扫描和胸部X线平片,结果显示无转移。患者接受了甲氨蝶呤、达卡巴嗪、环磷酰胺、放线菌素D和长春新碱的放化疗,但因严重毒性不得不改为长春新碱、放线菌素D、环磷酰胺和阿霉素方案。他完成了五个周期的化疗,毒性反应较轻。如今,诊断后6年,患者情况良好,无疾病复发。

结论

最近有关影响睾丸旁区域的促纤维增生性小圆细胞瘤的综述显示,与腹部肿瘤相比,这种起源的肿瘤预后较好。我们应将此病变纳入睾丸旁肿瘤的鉴别诊断中,主要是在儿童和青少年中。

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