Department of Hematology, National Hospital Organization Iwakuni Clinical Center, Iwakuni, Japan.
Department of Hematology, Oncology, and Respiratory Medicine, Okayama University Medical School, Okayama, Japan.
J Clin Exp Hematop. 2023;63(1):37-42. doi: 10.3960/jslrt.22038.
A 71-year-old Japanese man presented with severe thrombocytopenia. A whole-body CT at presentation showed small cervical, axillary, and para-aortic lymphadenopathy, leading to suspicion of immune thrombocytopenia due to lymphoma. Biopsy was difficult to perform because of severe thrombocytopenia. Thus, he received prednisolone (PSL) therapy and his platelet count gradually recovered. Two and a half years after PSL therapy initiation, his cervical lymphadenopathy slightly progressed without other clinical symptoms. Hence, a biopsy from the left cervical lymph node was performed, and he was diagnosed with nodal peripheral T-cell lymphoma (PTCL) with T follicular helper (TFH) phenotype. Due to various complications, we continued treatment with prednisolone alone after the diagnosis of lymphoma; however, there was no further increase in lymph node enlargement and no other lymphoma-related symptoms for one and a half years after diagnosis. Although immunosuppressive therapy has been reported to produce a response in some patients with angioimmunoblastic T-cell lymphoma, our experience suggests that a similar subset may exist in patients with nodal PTCL with TFH phenotype, which has the same cellular origin. Immunosuppressive therapies may constitute an alternative treatment option even in the era of novel molecular-targeted therapies, especially for elderly patients who are ineligible for chemotherapy.
一位 71 岁的日本男性因严重血小板减少症就诊。初次就诊时的全身 CT 显示颈、腋窝和腹主动脉旁小淋巴结病,这导致怀疑因淋巴瘤导致免疫性血小板减少症。由于严重血小板减少症,活检难以进行。因此,他接受了泼尼松龙(PSL)治疗,其血小板计数逐渐恢复。PSL 治疗开始后两年半,他的颈淋巴结病略有进展,无其他临床症状。因此,对左侧颈淋巴结进行了活检,诊断为具有滤泡辅助 T 细胞(TFH)表型的结外周 T 细胞淋巴瘤(PTCL)。由于存在各种并发症,我们在诊断为淋巴瘤后仅继续用泼尼松龙治疗;然而,在诊断后一年半的时间里,淋巴结肿大没有进一步增加,也没有其他与淋巴瘤相关的症状。尽管免疫抑制疗法已被报道在一些血管免疫母细胞性 T 细胞淋巴瘤患者中产生反应,但我们的经验表明,具有相同细胞起源的 TFH 表型结 PTCL 患者中可能存在类似的亚组,免疫抑制疗法可能构成一种替代治疗选择,即使在新型分子靶向治疗时代也是如此,特别是对于不适合化疗的老年患者。