Am J Hematol. 2010 Sep;85(9):727-9. doi: 10.1002/ajh.21774.
Hepatosplenic T cell lymphoma (HSTL) is a rare condition usually with an aggressive course and a poor prognosis even after extensive treatment. We describe here a patient who presented with hemophagocytosis. The lymphoma had unusual phenotypic features, an indolent course and responded to 20-deoxycoformycin therapy as a single agent. We suggest that this therapy be used in further cases as part of the treatment strategy.
肝脾 T 细胞淋巴瘤(HSTL)是一种罕见病症,通常具有侵袭性病程和不良预后,即使经过广泛治疗也是如此。我们在此描述了一位表现为噬血细胞现象的患者。该淋巴瘤具有非典型的表型特征,呈惰性病程,并且作为单一药物对 20-脱氧科福霉素治疗有反应。我们建议在进一步的病例中作为治疗策略的一部分使用这种治疗方法。