Chai Jing, Wang Yue, Mu Rong, Zhao Jinxia
Department of Rheumatology, Peking University Third Hospital, Beijing 100191, China.
Department of Lymphoma Internal Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2024 Dec 18;56(6):1115-1118. doi: 10.19723/j.issn.1671-167X.2024.06.028.
We reported the diagnostic and therapeutic process of a young male patient with systemic lupus erythematosus (SLE) who presented with severe hyponatremia as the main manifestation upon admission, and analyzed and discussed the case. The patient was a 19-year-old young male with a subacute course of disease, fever ≥38.3 ℃ that could not be explained by other causes, acute and subacute cutaneous lupus erythematosus, oral ulcers, arthritis, leukopenia (< 4×10/L), low C3+low C4, and positive anti-double-stranded DNA (anti-dsDNA). According to the 2019 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria, the score was 27 points. The patient was admitted to the hospital with SLE. After admission, further diagnosis of lupus was confirmed, excluding infection, tumor, endocrine disease, . Hyponatremia was the main complication of this lupus patient. Hyponatremia was a rare complication of lupus, only a few cases have been reported. In this study, the paient ' s blood osmotic pressure was significantly reduced, which was considered to be hypotonic hyponatretic, urine osmotic pressure increased, maximum urine dilution caused by excessive water intake such as primary polydipsia, hypoosmotic fluid intake, and beer drinking were excluded, and 24 h urine volume and sodium were improved. The urinary sodium concentration was close to 20 mmol/L although with severe hyponatremia, considering the possibility of isovolemic hypotonic hyponatremia, the syndrome of improper secretion of antidiuretic hormone or adrenal cortical insufficiency. The patient had no manifestations, such as hypotension, typical site pigmentation, and high potassium, and there was little possibility of adrenal cortical insufficiency, and syndrome of inappropriate antidiuretic hormone secretion (SIADH) was considered for hyponatremia in the patient. The etiological mechanism of hyponatremia in lupus patients is not clear, but it is related to acute kidney injury, drugs and systemic inflammation. In this case, we reported for the first time that SLE was associated with abnormal hypothalamic signals, suggesting a possible mechanism of lupus hyponatremia. The patient underwent water restriction, intravenous and oral sodium supplementation, and the blood sodium quickly returned to normal after pulse therapy. The abnormal signal of the head magnetic resonance imaging (MRI) fornix column was improved after 1 month of treatment, further confirming our diagnosis. SLE complicated with hyponatremia is rare, but severe hyponatremia can be life-threatening, and attention should be paid to it. The possibility of neuropsychiatric lupus should be vigilant in patients with lupus combined with hyponatremia.
我们报告了一名年轻男性系统性红斑狼疮(SLE)患者的诊断和治疗过程,该患者入院时以严重低钠血症为主要表现,并对该病例进行了分析和讨论。患者为19岁年轻男性,病程亚急性,有≥38.3℃的发热且无法用其他原因解释,有急性和亚急性皮肤型红斑狼疮、口腔溃疡、关节炎、白细胞减少(<4×10⁹/L)、C3降低+C4降低,以及抗双链DNA(抗dsDNA)阳性。根据2019年美国风湿病学会/欧洲抗风湿病联盟(ACR/EULAR)分类标准,得分27分。该患者因SLE入院。入院后,进一步确诊为狼疮,排除了感染、肿瘤、内分泌疾病等。低钠血症是该狼疮患者的主要并发症。低钠血症是狼疮罕见的并发症,仅有少数病例报道。在本研究中,患者血液渗透压显著降低,考虑为低渗性低钠血症,尿渗透压升高,排除了因饮水过多如原发性烦渴、低渗液摄入及饮用啤酒导致的最大尿稀释,24小时尿量及尿钠改善。尽管严重低钠血症,但尿钠浓度接近20mmol/L,考虑等渗性低渗性低钠血症、抗利尿激素分泌不当综合征或肾上腺皮质功能不全的可能性。患者无低血压、典型部位色素沉着及高钾血症等表现,肾上腺皮质功能不全可能性小,考虑患者低钠血症为抗利尿激素分泌不当综合征(SIADH)。狼疮患者低钠血症的病因机制尚不清楚,但与急性肾损伤、药物及全身炎症有关。在本病例中,我们首次报道SLE与下丘脑信号异常有关,提示狼疮低钠血症的一种可能机制。患者接受了限水、静脉及口服补钠治疗,脉冲治疗后血钠迅速恢复正常。治疗1个月后头部磁共振成像(MRI)穹窿柱异常信号改善,进一步证实了我们的诊断。SLE合并低钠血症罕见,但严重低钠血症可危及生命,应予以重视。狼疮合并低钠血症患者应警惕神经精神性狼疮的可能性。