Javed Aashir, Zhyzhneuskaya Sviatlana, Khalid Narmeen, Rajabally Hanaa
General Internal Medicine, University Hospital of North Durham, Durham, GBR.
Diabetes and Endocrinology, University Hospital of North Durham, Durham, GBR.
Cureus. 2024 Nov 5;16(11):e73037. doi: 10.7759/cureus.73037. eCollection 2024 Nov.
A male patient in his 30s with autism and depression presented to the emergency department with joint pain, a petechial/purpuric rash, sputum production, hemoptysis, and epistaxis. His mother reported a family history of autoimmune conditions. Examination revealed a non-blanching petechial/purpuric rash and tenderness in the feet and ankles. Elevated inflammatory markers, non-blanching rash, previous history of meningitis, and a chest X-ray with patchy opacifications with new oxygen requirements prompted empirical antibiotics and steroids to cover for a chest and possible central nervous system (CNS) infection. Despite antibiotics, inflammatory markers kept rising, necessitating a switch to broad-spectrum antibiotics with subsequent clinical improvement. Later, a positive anti-proteinase 3 antibody test and a CT chest scan showing bilateral ground glass opacities confirmed granulomatosis with polyangiitis (GPA). Management included a weaning course of steroids, proton pump inhibitors, and rituximab infusions. This case highlights the need to consider autoimmune conditions like GPA in autistic patients with multi-system involvement.
一名30多岁患有自闭症和抑郁症的男性患者因关节疼痛、瘀点/紫癜性皮疹、咳痰、咯血和鼻出血前往急诊科就诊。他的母亲报告有自身免疫性疾病家族史。检查发现有不褪色的瘀点/紫癜性皮疹以及足部和脚踝压痛。炎症指标升高、不褪色皮疹、既往脑膜炎病史以及胸部X线显示有斑片状模糊影且有新的吸氧需求,促使给予经验性抗生素和类固醇药物,以应对肺部及可能的中枢神经系统(CNS)感染。尽管使用了抗生素,炎症指标仍持续升高,因此改用广谱抗生素,随后临床症状有所改善。后来,抗蛋白酶3抗体检测呈阳性,胸部CT扫描显示双侧磨玻璃影,确诊为肉芽肿性多血管炎(GPA)。治疗包括逐渐减量的类固醇疗程、质子泵抑制剂和利妥昔单抗输注治疗。该病例强调,对于有多系统受累的自闭症患者,需要考虑像GPA这样的自身免疫性疾病。