孤立性粒细胞肉瘤:三例罕见病例报告及回顾

Eunpi Cho , Joshua Schiffer , Kathleen Murphy , B. Douglas Smith
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引用次数: 0

摘要

粒细胞肉瘤是一种罕见的髓外肿瘤,由未成熟的髓样细胞组成。传统上,这些肿瘤出现在已知的白血病患者中;然而,粒细胞肉瘤可能作为一种孤立的发现出现在没有已知疾病的患者中。因此,孤立性粒细胞肉瘤可能对临床医生照顾患者提出诊断挑战。此外,这些肿瘤也给临床医生带来了治疗上的挑战,因为它们通常预后较差,并且对以阿糖胞苷为基础的化疗的全身治疗往往只有短暂的反应。对粒细胞肉瘤生物学的进一步了解可能会揭示肿瘤领域正在研究的一些新的生物活性药物的靶点。本文报告了粒细胞肉瘤的三种常见表现,并简要回顾了已知的病理生理学,提醒我们要改善患者的预后还有很多工作要做。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated Granulocytic Sarcoma: Case Reports of Three Rare Presentations and Review

Granulocytic sarcomas are rare, extramedullary tumors composed of immature myeloid cells. Traditionally, these tumors present in patients with known leukemias; however, granulocytic sarcomas may present as an isolated finding in patients without known disease. As such, isolated granulocytic sarcomas may present a diagnostic challenge for clinicians taking care of the patient. Moreover, these tumors also create a therapeutic challenge for clinicians as they generally carry a poor prognosis and often have short-lived responses to systemic therapy with cytarabine-based chemotherapy. An improved understanding of the biology of granulocytic sarcomas may reveal targets accessible to some of the new biologically active agents being studied across oncology. This report of 3 usual presentations of granulocytic sarcomas and a brief review of the known pathophysiology reminds us that there is much work to do to improve outcomes for our patients.

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