The discovery of multiple myeloma during the evolution of lupus nephropathy: A case report and literature review

Ameth Dieng, Mame Selly Diawara, Mouhamadou Moustapha Cisse
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Abstract

Introduction: Systemic lupus erythematosus (SLE) has been proven to be independently associated with higher proportions of malignancies, particularly hematological patterns. We report a patient who developed multiple myeloma on underlying lupus nephropathy with poor outcome. Observation: It was a 48-year-old male patient followed in pneumology for bronchial dilatation secondary to pulmonary tuberculosis who consulted nephrology for an impure nephrotic syndrome without extra-renal signs and a renal biopsy outlining advanced endo and extra-capillary glomerulonephritis with 38% activity. The etiological investigation had revealed lupus. Despite 2 therapeutic protocols based on MMF + corticoids then cyclophosphamide + corticoids, there was no remission. He underwent conservative treatment for chronic kidney disease with stable renal function including a GFR of 27 ml/min/1.73m2. Two years after the discovery of lupus disease, the patient presented with a bleeding syndrome with a blood count showing normocytic normochromic anaemia at 4.1 g/dl, leukopenia at 830/mm3 and thrombocytopenia at 49000/mm3. The bone marrow count performed on the basis of this pancytopenia showed a plasmocytosis in 38% with a dysmorphic erythroblastic lineage (basophilic punctation and laminated cytoplasm), an absent megakaryocytic lineage and the presence of numerous naked plasma cells and dysmorphic plasma cells, numerous hemophagocytic macrophages and siderophages. Plasma protein electrophoresis did not show a monoclonal peak. The outcome was poor. Death occurred 3 days after his hospitalization in a medullary insufficiency course. Conclusion: Lupus can be the starting point for the development of a hematological malignancy at a later stage. On the other hand, cancer can induce spontaneous autoimmune manifestations or secondary to anti-tumor therapies. In our case it was a patient who developed myeloma 2 years after the onset of lupus with a poor outcome leading to death.
狼疮肾病发展过程中多发性骨髓瘤的发现:1例报告及文献复习
系统性红斑狼疮(SLE)已被证明与较高比例的恶性肿瘤,特别是血液学模式独立相关。我们报告一个病人谁发展多发性骨髓瘤的潜在狼疮肾病与不良预后。观察:这是一名48岁男性患者,因继发于肺结核的支气管扩张接受了肺炎学检查,他向肾脏病科咨询了不纯肾病综合征,无肾外体征,肾活检显示晚期终末和毛细血管外肾小球肾炎,活动性为38%。病因调查显示为狼疮。尽管有MMF +皮质激素和环磷酰胺+皮质激素两种治疗方案,但没有缓解。慢性肾病保守治疗,肾功能稳定,GFR 27 ml/min/1.73m2。在发现狼疮疾病两年后,患者出现出血综合征,血液计数显示:正红细胞正色贫血4.1 g/dl,白细胞减少830/mm3,血小板减少49000/mm3。在全血细胞减少的基础上进行的骨髓计数显示,38%的患者浆细胞增多,伴有畸形红细胞谱系(嗜碱性点和层状细胞质),巨核细胞谱系缺失,存在大量裸浆细胞和畸形浆细胞,大量噬血细胞巨噬细胞和侧噬细胞。血浆蛋白电泳未见单克隆峰。结果很糟糕。患者住院3天后因髓质功能不全死亡。结论:狼疮可能是血液学恶性肿瘤晚期发展的起点。另一方面,癌症可诱发自发的自身免疫表现或继发于抗肿瘤治疗。在我们的病例中,患者在狼疮发病2年后患上骨髓瘤,预后不佳导致死亡。
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