Rheumatology Department, Mongi Slim Hospital, La Marsa, Tunisia.
Urology Department, La Rabta Hospital, Tunis, Tunisia.
CEN Case Rep. 2021 May;10(2):165-171. doi: 10.1007/s13730-020-00537-y. Epub 2020 Sep 28.
Renal involvement in large B-cell lymphoma represents an exceptional manifestation of non-Hodgkin lymphomas. Renal failure and bone metastasis by lymphomatous infiltration is extremely rare. We describe a 46-year-old woman presenting with a renal failure and a 5-month history of intermittent left knee pain that was previously misdiagnosed with osteoarthritis. It was due to a bilateral primary renal lymphoma (PRL) associated with bone metastasis. Knee MRI showed a permeative lesion and an abnormal signal in the metaphysis and diaphysis of the left proximal tibia with periosteal reaction and surrounding soft tissue swelling. The CT body scan showed a bilateral nephromegaly and multiple lytic bone lesion of aggressive appearance at the right iliac wing and right sacral ala evoking lymphomatous involvement. Node biopsy with immunohistochemistry study confirmed a diagnosis of large B-cell lymphoblastic lymphoma. In this article, we focus on clinical, radiological, immunohistochemical presentation, differential diagnosis and review the literature. Ten cases including our case were reported in our literature review of both renal and bone lymphoma. There was a male predominance, with a mean age of 55.1 years old. We noted a high frequency of renal failure in diagnosis. In X-rays, the metaphysis is the most common site of occurrence in long bones and the main sign was osteolytic bone destruction. The subtype of lymphoma was DLBCL stage IV in most cases except in one case where it was a hystiocytic lymphoma. Finally, prognosis was poor, more than half of patients died. PRL with bone metastasis is a rare malignancy that is difficult to diagnose. Clinicians should increase the awareness of the disease and consider a differential diagnosis of bone lesions. Early diagnosis and active treatment can improve patient prognosis.
肾脏受累于大 B 细胞淋巴瘤是非霍奇金淋巴瘤的一种特殊表现。淋巴瘤浸润导致肾衰竭和骨转移极为罕见。我们描述了一位 46 岁的女性,她因肾衰竭和 5 个月间歇性左膝痛就诊,此前被误诊为骨关节炎。病因是双侧原发性肾淋巴瘤(PRL)合并骨转移。膝关节 MRI 显示左侧胫骨近端弥漫性病变和骨干骺端异常信号,伴有骨膜反应和周围软组织肿胀。CT 全身扫描显示双侧肾脏增大和右侧髂骨翼和右侧骶骨翼多处溶骨性骨病变,呈侵袭性表现,提示淋巴瘤累及。淋巴结活检和免疫组化研究证实为大 B 细胞淋巴母细胞淋巴瘤。本文重点介绍了临床表现、影像学表现、免疫组化表现、鉴别诊断,并复习了文献。在我们对肾和骨淋巴瘤的文献复习中,包括我们的病例共报告了 10 例。该疾病以男性为主,平均年龄为 55.1 岁。我们注意到诊断时肾衰竭的发生率较高。在 X 光片上,长骨中最常见的发生部位是干骺端,主要征象是溶骨性骨破坏。除了一例为组织细胞淋巴瘤外,大多数情况下淋巴瘤的亚型为 DLBCL Ⅳ期。最后,预后较差,超过一半的患者死亡。伴骨转移的 PRL 是一种罕见的恶性肿瘤,难以诊断。临床医生应提高对该病的认识,并考虑骨病变的鉴别诊断。早期诊断和积极治疗可以改善患者的预后。