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Grade 4 unclassified renal cell carcinoma with sarcomatoid component expressing S-100 protein. A case report with peculiar diagnostic and therapeutic implications

机译:肉瘤样成分表达S-100蛋白的4级未分类肾细胞癌。具有特殊诊断和治疗意义的病例报告

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摘要

Grade 4 unclassified renal cell carcinoma, with a sarcomatoid component (URCCSC) is a rare high grade tumor presumptively derived from all histological subtypes of renal cell carcinoma (RCC). Even though rare, URCCSC generates a great deal of interest, as it is a particularly aggressive variant of RCC, that is poorly responsive to chemo-immunotherapy. Whether it originates from a separate sarcomatoid cell clone within the tumor or from true cell dedifferentiation from RCC has yet to be established. The diagnosis of URCCSC is usually based on morphological and immunohistochemical characteristics of the neoplastic cells which show transitional epithelial/mesenchymal features. In fact, the frequent loss of epithelial markers and gain of mesenchymal phenotypes, can result in difficulties in interpreting diagnostic data. Consequently assigning the optimal therapeutic treatments can be hindered due to this biological “complexity." Here we present the clinicopathological records of a 51 year-old patient who underwent an excision of a periureteral retroperitoneal mass, and whose first pathological diagnosis was malignant peripheral nerve sheath tumor (MPNST). Eleven months after surgery, a CT-scan revealed a local recurrence of the disease. Later on the patient was admitted to our hospital and a systemic, sarcoma-oriented, treatment was initiated. A partial remission was observed but only with a dacarbazine based regimen administered as a third line therapy, after which a second surgery took place. The removed tumor was diagnosed as URCCSC based on the peculiar morphologic and immunohistochemical characteristics of the cells. Pathological assessment of the first intervention was re-evaluated, resulting in a diagnosis of URCCSC. This case-report therefore highlights the implications that an erroneous pathologic diagnosis can have for the clinical management of this disease. Furthermore, the unexpected response to a dacarbazine based regimen, indicates that this drug should be included among the therapeutic options available against this type of renal carcinoma.
机译:具有肉瘤样成分(URCCSC)的4级未分类肾细胞癌是一种罕见的高级别肿瘤,推测是源自肾细胞癌(RCC)的所有组织学亚型。尽管很少见,但URCCSC引起了极大的兴趣,因为它是RCC的一种特别具有侵略性的变体,对化学免疫疗法的反应较差。它是否起源于肿瘤内的单独的肉瘤样细胞克隆或源自RCC的真正细胞​​去分化尚待确定。 URCCSC的诊断通常基于显示过渡性上皮/间充质特征的肿瘤细胞的形态和免疫组织化学特征。实际上,上皮标记物的频繁丢失和间充质表型的获得可能会导致难以解释诊断数据。因此,由于这种生物学上的“复杂性”,可能会阻碍分配最佳治疗方法。在这里,我们介绍了一名51岁患者的临床病理记录,该患者接受了输尿管周围腹膜后肿块的切除,并且其首次病理诊断是恶性周围神经鞘膜肿瘤(MPNST),术后11个月,CT扫描显示该病已局部复发,随后患者入院并开始全身性肉瘤治疗,观察到部分缓解,但仅给予达卡巴嗪为基础的方案作为第三线疗法,然后进行第二次手术,根据细胞的独特形态和免疫组化特征,将切除的肿瘤诊断为URCCSC,重新评估了第一次干预的病理学评估,导致对URCCSC的诊断。因此,此病例报告强调了错误病态的含义。逻辑诊断可以对该疾病进行临床管理。此外,对基于达卡巴嗪的方案的出乎意料的反应表明,该药物应包括在针对此类肾癌的可用治疗选择中。

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