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Clinicopathological features diagnosis and treatment of clear cell sarcoma/melanoma of soft parts

机译:软组织透明细胞肉瘤/黑色素瘤的临床病理特征诊断和治疗

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摘要

>Background: Clear cell sarcoma of tendons and aponeuroses is a rare, high grade malignant soft tissue tumor resembling melanoma and soft tissue sarcomas.>Clinical and Imaging Presentation: The median age at presentation is 27 years and the most common location are the foot and the ankle. MR imaging typically shows a benign looking, well defined, homogenous mass; on T1-weighted MR images, it is usually homogeneous and isointense or slight hyperintense to muscle, whereas on T2-weighted MR images, it is usually more heterogeneous with variable signal intensity.>Pathology: Microscopically, the clear cell appearance is due to the accumulation of glycogen. The cells show no or minimal pleomorphism, and paucity of mitotic figures that is in concordance with the slow-growing behavior of the tumor. Scattered multinucleated giant cells are commonly present; areas of necrosis and melanin pigment may be identified. The reciprocal translocation t(12;22)(q13;q12) is observed in more than 90% of clear cell sarcoma cases. In addition, polysomy of chromosome 8 has been observed as a secondary abnormality in many cases of clear cell sarcoma. The differential diagnosis of clear cell sarcoma should include melanoma, epithelioid malignant peripheral nerve sheath tumor, melanotic schwannoma, paraganglioma-like dermal melanocytic tumor, perivascular epithelioid cell neoplasms (PEComas), cellular blue naevus, synovial sarcoma (monophasic type), alveolar soft part sarcoma, paraganglioma, epithelioid sarcoma and carcinomas. Treatment and Prognosis: The treatment of choice for clear cell sarcoma is wide surgical resection. If complete excision is achieved, adjuvant treatments are not unnecessary. Chemotherapy is predominantly employed in patients with metastatic disease. The 5 to 20 year survival of the patients with clear cell sarcoma range from 67% to 10%. The rates of local recurrence ranges up to 84%, late metastases up to 63%, and metastases at presentation up to 30%.
机译:>背景:肌腱和腱膜的透明细胞肉瘤是一种罕见的,高度恶性的类似于黑色素瘤和软组织肉瘤的恶性软组织肿瘤。>临床和影像学表现:是27岁,最常见的位置是脚和脚踝。 MR成像通常显示出良性外观,轮廓分明的均匀质量。在T1加权MR图像上,它通常对肌肉均匀且等强度或轻微高强度,而在T2加权MR图像上,它通常具有更不均匀的信号强度。>病理:细胞外观是由于糖原的积累。这些细胞没有或只有很少的多态性,并且与肿瘤的缓慢生长行为一致的缺乏有丝分裂图。分散的多核巨细胞通常存在。可以确定坏死区域和黑色素色素。在超过90%的透明细胞肉瘤病例中观察到相互易位t(12; 22)(q13; q12)。此外,在许多透明细胞肉瘤病例中,已观察到8号染色体的多体性是继发性异常。透明细胞肉瘤的鉴别诊断应包括黑色素瘤,上皮样恶性周围神经鞘瘤,黑色素神经鞘瘤,副神经节瘤样皮肤黑素细胞瘤,血管周上皮样细胞瘤(PEComas),细胞蓝色痣,滑膜肉瘤(单相型),肺泡软部分肉瘤,副神经节瘤,上皮样肉瘤和癌。治疗和预后:透明细胞肉瘤的治疗选择是广泛的手术切除。如果完全切除,则不需要辅助治疗。转移性疾病患者主要使用化学疗法。透明细胞肉瘤患者的5至20年生存率在67%至10%之间。局部复发率高达84%,晚期转移率高达63%,表现时的转移率高达30%。

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