[Two cases of successfully treated intravascular lymphoma presenting with fever and dyspnea].

Ayako Sakurai, Keisuke Tomii, Akane Haruna, Nobuyuki Katakami, Yutaka Takahashi, Yukihiro Imai
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引用次数: 0

Abstract

We report two patients with intravascular large B-cell lymphoma who presented with fever and dyspnea. Serum level of lactate dehydrogenase (LDH) and soluble interleukin-2 receptor (sIL-2R) levels were extremely high in both cases. Chest CT revealed tumor mass and ground glass opacity in one patient, and no abnormality in another patient who had severe hypoxemia. Their perfusion ventilation lung scintigraphy demonstrated multiple defects, and gallium scintigraphy showed abnormal accumulation in both lungs, and the spleen. Both patients were successfully treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). Initial chemotherapy was followed by high dose systemic chemotherapy with peripheral blood stem cell support. Intravascular large B-cell lymphoma should always be considered in the differential diagnosis of fever and hypoxemia with elevated serum LDH and sIL-2R, regardless of the chest CT findings.

[2例成功治疗的血管内淋巴瘤,表现为发热和呼吸困难]。
我们报告了两例血管内大b细胞淋巴瘤患者,他们表现为发烧和呼吸困难。两例患者血清乳酸脱氢酶(LDH)和可溶性白介素-2受体(sIL-2R)水平均极高。1例胸部CT显示肿瘤肿块及磨玻璃影,另1例严重低氧血症患者未见异常。灌注通气肺显像显示多处缺陷,镓显像显示双肺和脾脏异常积聚。两例患者均成功接受利妥昔单抗、环磷酰胺、阿霉素、长春新碱和强的松(R-CHOP)治疗。初始化疗后采用外周血干细胞支持的大剂量全身化疗。无论胸部CT表现如何,在伴有血清LDH和sIL-2R升高的发热和低氧血症的鉴别诊断中,都应考虑血管内大b细胞淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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