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A case of cutaneous clear cell sarcoma determined by clinicopathological and cytogenetic analysis

机译:通过临床病理和细胞遗传学分析确定皮肤透明细胞肉瘤1例

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Cutaneous clear cell sarcoma (CCS) is a rare soft tissue malignancy that typically manifests in the distal extremities of young adults. Although it shows melanocytic differentiation, CCS is clearly pathologically and genetically distinct from malignant melanoma. Here, we report the case of a 43-year-old male who had an asymptomatic, deep-seated, slowly enlarging, firm mass over the right heel for 30 years that recently and rapidly progressed with tenderness. We arranged for the total excision of the tumor. Pathological and cytogenetic analysis of the biopsied specimen showed that it was a clear cell sarcoma. Computed tomography and positron emission tomography scans showed no signs of metastasis, and no other abnormal hypermetabolic lesions were detected. Wide excision with split-thickness skin graft and a sentinel lymph node biopsy were performed. Because of positive findings in the sentinel lymph nodes, the patient was transferred to the plastic surgery department for further radical popliteal and inguinal lymph node dissection. The patient has received regular outpatient follow-up care in our hospital for the past 8 months with no evidence of recurrence.
机译:皮肤透明细胞肉瘤(CCS)是一种罕见的软组织恶性肿瘤,通常表现在年轻人的远端。尽管CCS显示出黑素细胞分化,但在病理学和遗传学上显然与恶性黑色素瘤不同。在这里,我们报道了一个43岁男性的案例,该男性在右足跟上有30年无症状,根深蒂固,缓慢增大的坚硬肿块,最近又随着压痛迅速发展。我们安排了肿瘤的全部切除。活检标本的病理和细胞遗传学分析表明,它是透明细胞肉瘤。计算机体层摄影术和正电子发射体层摄影术扫描未显示转移迹象,也未检测到其他异常的代谢异常病变。进行了广泛的切除术,使用了裂厚的皮肤移植物并进行了前哨淋巴结活检。由于前哨淋巴结的阳性发现,该患者被转移到整形外科进行进一步的pop骨和腹股沟淋巴结清扫术。该患者在过去8个月中在我院接受了定期门诊随访,没有复发的迹象。

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