Dubai Fatema M, Isa Ahmed
Internal Medicine, Salmaniya Medical Complex, Manama, BHR.
Emergency, Shifa Al Jazeera Medical Center, Manama, BHR.
Cureus. 2023 Jan 11;15(1):e33664. doi: 10.7759/cureus.33664. eCollection 2023 Jan.
Overlap syndrome refers to a large group of inflammatory rheumatic conditions characterized by the co-existence of clinical manifestations that include different organ systems and meet the criteria of more than one rheumatic disease. Overlap syndromes are less common compared with the conditions they encompass, for example, the global prevalence of systemic lupus erythematosus (SLE) is estimated to be 43.7 per 100,000 persons, of which only around 3.4-6.3% present with SLE-myositis overlap. Although rare, overlap syndromes commonly include lupus, rheumatoid arthritis, scleroderma, and myositis. Because overlap syndrome can manifest in several ways and has an unpredictable course, it poses a challenge to multidisciplinary teams that examine and treat patients. Therefore, we must not disregard any signs and symptoms as they might have a huge impact on the progression of the disease and the overall outcome of the treatment. We present a rare case of SLE-myositis overlap syndrome in a 44-year-old male. He initially presented with gradual weakness in the proximal muscles of the bilateral lower limb. This patient was diagnosed as having SLE with positive 5g protein/24 hours, anti-nuclear, low C3, anti-U1RNP, anti-Ro, and anti-La antibodies, as well as membranous lupus nephritis evident by the results of renal biopsy. The diagnosis of myositis was also made according to the history and evaluation of the patient, the high titer of muscle enzymes creatine kinase level, and MRI result. Although the patient tested positive for anti-U1RNP, he did not meet the criteria of mixed connective tissue disease. Eventually, the patient was found to have overlap syndrome. The prevalence of overlap between SLE and myositis is relatively rare and varies from 3.4% to 6.3%. To our knowledge, no study has discussed or reported its prevalence among males.
重叠综合征是指一大类炎症性风湿性疾病,其特征是临床表现同时累及不同器官系统,且符合不止一种风湿性疾病的标准。与它们所包含的疾病相比,重叠综合征相对少见,例如,系统性红斑狼疮(SLE)的全球患病率估计为每10万人中有43.7例,其中只有约3.4 - 6.3%表现为SLE - 肌炎重叠。尽管罕见,但重叠综合征通常包括狼疮、类风湿关节炎、硬皮病和肌炎。由于重叠综合征可以有多种表现方式且病程不可预测,这对检查和治疗患者的多学科团队构成了挑战。因此,我们绝不能忽视任何体征和症状,因为它们可能对疾病的进展和治疗的总体结果产生巨大影响。我们报告一例44岁男性的罕见SLE - 肌炎重叠综合征病例。他最初表现为双侧下肢近端肌肉逐渐无力。该患者被诊断为SLE,24小时尿蛋白5g阳性、抗核抗体阳性、C3降低、抗U1RNP、抗Ro和抗La抗体阳性,肾活检结果显示为膜性狼疮性肾炎。根据患者的病史和评估、肌肉酶肌酸激酶水平的高滴度以及MRI结果,也做出了肌炎的诊断。尽管该患者抗U1RNP检测呈阳性,但他不符合混合性结缔组织病的标准。最终,该患者被发现患有重叠综合征。SLE和肌炎重叠的患病率相对罕见,在3.4%至6.3%之间。据我们所知,尚无研究讨论或报告其在男性中的患病率。