强的松龙单独治疗伴有T滤泡辅助表型的淋巴结周围T细胞淋巴瘤的益处。

IF 0.9 Q4 HEMATOLOGY
Wataru Kitamura, Hiroki Kobayashi, Tomohiro Urata, Yumiko Sato, Yusuke Naoi, Tadashi Yoshino, Yoshinobu Maeda, Shoichi Kuyama
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引用次数: 0

摘要

一名71岁的日本男性表现为严重的血小板减少症。表现时全身CT显示颈部、腋窝和主动脉旁小淋巴结病变,怀疑淋巴瘤引起的免疫性血小板减少症。由于严重的血小板减少症,活检很难进行。因此,他接受强的松龙(PSL)治疗,血小板计数逐渐恢复。PSL治疗开始2年半后,患者宫颈淋巴结病变轻微进展,无其他临床症状。因此,对左颈部淋巴结进行活检,诊断为淋巴结外周T细胞淋巴瘤(PTCL)伴T滤泡辅助型(TFH)表型。由于各种并发症,我们在诊断为淋巴瘤后继续单用强的松龙治疗;然而,在诊断后的一年半内,淋巴结肿大没有进一步增加,也没有其他淋巴瘤相关症状。虽然免疫抑制疗法已被报道在一些血管免疫母细胞t细胞淋巴瘤患者中产生应答,但我们的经验表明,在具有TFH表型的淋巴结性PTCL患者中可能存在类似的亚群,其具有相同的细胞起源。即使在新的分子靶向治疗时代,免疫抑制疗法也可能构成一种替代治疗选择,特别是对于不适合化疗的老年患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Benefit of prednisolone alone in nodal peripheral T-cell lymphoma with T follicular helper phenotype.

Benefit of prednisolone alone in nodal peripheral T-cell lymphoma with T follicular helper phenotype.

Benefit of prednisolone alone in nodal peripheral T-cell lymphoma with T follicular helper phenotype.

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.

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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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