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目的探讨粒细胞肉瘤临床特点及治疗措施,提高对其认识。方法结合1例粒细胞肉瘤患者的临床资料和相关文献复习,详细分析该病的临床特点、病理特征、诊断治疗及预后。结果粒细胞肉瘤是一种少见的生长于髓外、由未成熟的髓样细胞构成的肿瘤。放化疗后效果较好,临床随访未见复发。结论 GS十分罕见,易误诊为淋巴瘤,病理组织学检查是其诊断金标准,MPO是诊断特异性最高的标志物。
Objective To investigate the clinical features and treatment of granulocystic sarcoma and to improve their understanding. Methods A case of granulocystic sarcoma patients with clinical data and relevant literature review, a detailed analysis of the clinical features of the disease, pathological features, diagnosis and treatment and prognosis. Results Granulocytic sarcoma is a rare tumor that grows extramedullary and consists of immature myeloid cells. After radiotherapy and chemotherapy better, no recurrence of clinical follow-up. Conclusion GS is very rare, easily misdiagnosed as lymphoma, histopathological examination of gold is the gold standard, MPO is the highest diagnostic specificity markers.