Anorexia nervosa and systemic lupus erythematosus: a coincidence?

Maysoun Kudsi, Raghad Tarcha, Naram Khalayli, Ghina Haidar, Sana Btrush
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Abstract

The COVID-19 pandemic has led to a post-acute syndrome that can persist for an extended period. The correlation between anorexia nervosa (AN) and some autoimmune diseases has been reported. Systemic lupus erythematosus (SLE) is a systemic autoimmune disease, presented with different clinical ions and periods, affecting all ages, especially females. The coexistence of SLE and AN has been reported in rare cases. The authors present the case of a 22-year-old male with severe AN coexisting with SLE. We present a case of a 22-year-old male diagnosed with SLE. He also completely refused to eat and drink and presented with behavioral disorders and suicidal thoughts. He was on 200 mg/day of oral hydroxychloroquine, 400 units/day of vitamin D, and 1000 mg/day of oral calcium. There was no positive other history, trauma, drug addiction, or family history. AN was diagnosed according to ICD-10 and DSM-V. Physical examination revealed decreased subcutaneous tissue and muscle atrophy. The weight of the patient was 35.3 kg. Verbal contact was maintained, and psychotic symptoms were not observed. Tenderness in all joints was noticed, while swelling in both knees and right ankle joints was found. Laboratory tests revealed elevated inflammatory markers. Treatment includes a high-calorie diet administered by a feeding tube. The patient began to gain weight after 3 months. He is on 200 mg/day hydroxychloroquine, with remission till now January 2024. The novelty of our case is that it is a case of a young adult man presented with AN during mild lupus, who responded well to treatment with steroids and a high-calorie diet. Previous research has suggested the existence of a close link between food and eating disturbance and autoimmunity, and herein we provide further evidence to support this relationship by presenting a case report of an adult male with SLE and AN.
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神经性厌食症和系统性红斑狼疮:巧合?
COVID-19 大流行导致了一种可持续较长时间的急性后综合征。神经性厌食症(AN)与某些自身免疫性疾病之间的相关性已有报道。系统性红斑狼疮(SLE)是一种全身性自身免疫性疾病,临床表现和发病时期各不相同,影响各个年龄段,尤其是女性。系统性红斑狼疮和自闭症同时存在的病例很少见。作者介绍了一例 22 岁男性严重 AN 并发系统性红斑狼疮的病例。 我们介绍了一例被诊断为系统性红斑狼疮的 22 岁男性病例。他也完全拒绝进食和饮水,并伴有行为障碍和自杀念头。他每天口服 200 毫克羟氯喹、400 单位维生素 D 和 1000 毫克口服钙。他没有其他阳性病史、外伤史、吸毒史或家族史。AN 的诊断依据是 ICD-10 和 DSM-V。体格检查显示患者皮下组织减少,肌肉萎缩。患者体重为35.3公斤。患者能保持言语交流,未发现精神症状。所有关节均有触痛,双膝和右踝关节肿胀。实验室检查显示炎症指标升高。治疗包括通过喂食管进行高热量饮食。3 个月后,患者的体重开始增加。他每天服用 200 毫克羟氯喹,直到 2024 年 1 月病情才有所缓解。 我们这个病例的新颖之处在于,它是一个在轻度狼疮期间出现自闭症的年轻男性病例,对类固醇和高热量饮食的治疗反应良好。 以前的研究表明,食物和饮食紊乱与自身免疫之间存在着密切联系,我们在此提供了一个患有系统性红斑狼疮和自闭症的成年男性病例报告,进一步证明了这种关系。
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