Emorinken Airenakho, Erameh Cyril O, Eluehike Sylvester U, Dic-Ijiewere Mercy O, Ugheoke Asuwemhe J
Department of Internal Medicine, Irrua Specialist Teaching Hospital, Irrua, NGA.
Department of Radiology, Irrua Specialist Teaching Hospital, Irrua, NGA.
Cureus. 2021 Sep 3;13(9):e17679. doi: 10.7759/cureus.17679. eCollection 2021 Sep.
Systemic lupus erythematosus and syringomyelia are two distinct conditions with different pathogenetic pathways as well as diverse genetic and clinical characteristics. The coexistence of these two conditions has not been previously documented in the literature. We describe a 38-year-old male who presented with progressive bilateral weakness and pain in the lower limbs and loss of sphincteric functions three years following a diagnosis of lupus nephritis. Relevant autoantibody testing, hypocomplementemia, and biopsy-proven membranous lupus nephritis confirmed the diagnosis of systemic lupus erythematosus and magnetic resonance imaging of the spine confirmed the presence of syringomyelia. Therapy for lupus nephritis was instituted accordingly, while the patient was referred for neurosurgical intervention. The mechanism underlying syrinx formation in this patient is uncertain and, thus, further research is critical in this area.
系统性红斑狼疮和脊髓空洞症是两种不同的病症,具有不同的发病机制以及多样的遗传和临床特征。此前文献中尚未记载这两种病症并存的情况。我们描述了一名38岁男性,在被诊断为狼疮性肾炎三年后,出现双下肢进行性无力、疼痛以及括约肌功能丧失。相关自身抗体检测、低补体血症以及活检证实的膜性狼疮性肾炎确诊了系统性红斑狼疮,而脊柱磁共振成像证实存在脊髓空洞症。相应地开始了狼疮性肾炎的治疗,同时该患者被转诊接受神经外科干预。该患者脊髓空洞形成的机制尚不确定,因此,这一领域的进一步研究至关重要。