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True identity of endocapillary proliferation: a case of intravascular large B cell lymphoma diagnosed with immunohistochemical study of kidney biopsy and literature review

机译:毛细血管内增生的真实身份:一例经肾脏活检免疫组织化学诊断为血管内大B细胞淋巴瘤的病例并文献复习

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摘要

A 78-year-old Japanese female presented with low-grade fever, malaise, and appetite loss lasting for 1 month. Upper and lower gastrointestinal endoscopy and contrast-enhanced whole-body computed tomography (CT) revealed no abnormal findings at a referring hospital. She was referred to our hospital because of bilateral leg edema and 2.5 g/day proteinuria. Serum creatinine was 0.73 mg/dl and the kidneys were not enlarged. Kidney biopsy showed marked endocapillary proliferation with mesangiolysis. Soon after the kidney biopsy, her symptoms improved spontaneously, along with decreases in lactate dehydrogenase (LDH) from 503 to 197 IU/l, C-reactive protein (CRP) from 4.47 to 0.66 mg/dl, and soluble interleukin-2 receptor (sIL-2R) from 1789 to 1001 U/ml. Thus, she was followed carefully as an outpatient. One month later, however, she presented with dysarthria and right-sided hemiparesis, and diffusion-weighted brain magnetic resonance imaging (MRI) showed multiple high-intensity areas. She also had respiratory failure, and lung perfusion scintigraphy showed multiple low blood stream areas. Suspecting some endovascular abnormality, we performed immunohistochemical staining of the kidney biopsy specimen taken previously to find that endocapillary infiltrating cells were CD20-positive B lymphocytes. The infiltrating cells were confined to the endocapillary compartment in glomeruli and peritubular capillaries. Both clinical and pathological findings led us to diagnose intravascular large B cell lymphoma (IVLBCL). Two bone marrow biopsies and random skin biopsies were performed, but no abnormality was found. The present case demonstrates that clinical course and renal biopsy findings of intravascular large B cell lymphoma may mimic other renal conditions and that the identification of cell types with immunohistochemical staining may help establish an accurate diagnosis.
机译:一名78岁的日本女性表现为低烧,不适和食欲不振,持续1个月。上消化道内窥镜检查和下消化道内窥镜检查以及增强的全身计算机断层扫描(CT)在转诊医院未发现异常发现。由于双侧腿浮肿和2.5克/天的蛋白尿,她被转诊到我们医院。血清肌酐为0.73 mg / dl,肾脏未肿大。肾脏活检显示,伴有血管舒张的明显毛细血管内膜增生。肾脏活检后不久,她的症状自发改善,乳酸脱氢酶(LDH)从503降至197IU / l,C反应蛋白(CRP)从4.47降至0.66 mg / dl,可溶性白介素2受体( sIL-2R)从1789至1001U / ml。因此,她作为门诊患者受到了认真的跟踪。但是一个月后,她出现了构音障碍和右侧偏瘫,并且弥散加权脑磁共振成像(MRI)显示了多个高强度区域。她还患有呼吸衰竭,肺灌注显像显示多个低血流区域。怀疑某些血管内异常,我们对先前采集的肾脏活检标本进行了免疫组织化学染色,以发现毛细血管内浸润细胞为CD20阳性B淋巴细胞。浸润细胞局限于肾小球和肾小管毛细血管的毛细血管内腔。临床和病理学发现均促使我们诊断出血管内大B细胞淋巴瘤(IVLBCL)。进行了两次骨髓活检和随机皮肤活检,但未发现异常。本病例证明,血管内大B细胞淋巴瘤的临床病程和肾脏活检结果可模仿其他肾脏疾病,并且用免疫组织化学染色鉴定细胞类型可有助于建立准确的诊断。

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