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首页> 外文期刊>International journal of surgical pathology >Pediatric Renal Solitary Fibrous Tumor: Report of a Rare Case and Review of the Literature
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Pediatric Renal Solitary Fibrous Tumor: Report of a Rare Case and Review of the Literature

机译：小儿肾孤立性纤维性肿瘤：一例罕见病例报告及文献复习

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摘要

Solitary fibrous tumors (SFTs) are unusual spindle cell neoplasms initially described in the pleura but have since been discovered in many extrapleural locations. SFT of the kidney is extremely rare, the majority occurring in middle-aged adults. To date, only two pediatric cases of renal SFT have been reported. We report a case of large SFT in the kidney of a 3-year-old boy that was clinically and radiologically thought to be a nephroblastoma. This case is the first pediatric renal SFT to be reported with detailed histopathologic and cytogenetic analyses. SFT should be included in the differential diagnosis of pediatric renal tumors.
机译：孤立性纤维性肿瘤（SFT）是最初在胸膜中描述的不常见的纺锤体细胞瘤，但此后已在许多胸膜外部位发现。肾脏的SFT非常罕见，大多数发生在中年成年人中。迄今为止，仅报道了两个小儿肾脏SFT病例。我们报告了一个3岁男孩的肾脏中发生大型SFT的情况，该病例在临床和放射学上被认为是肾母细胞瘤。该病例是首例通过详细的组织病理学和细胞遗传学分析报告的小儿肾脏SFT。 SFT应包括在小儿肾肿瘤的鉴别诊断中。

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