Granulomatosis With Polyangiitis in an Autistic Patient With Depression: Challenges in Diagnosis and Management
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.
Authors
- Sviatlana Zhyzhneuskaya (ORCID: https://orcid.org/0000-0003-4501-2729)
- Afzal Javed (ORCID: https://orcid.org/0000-0003-2518-0688)
- Hanaa Rajabally (ORCID: https://orcid.org/0000-0003-1827-6526)
- Nauman Khalid (ORCID: https://orcid.org/0000-0002-8045-199X)
Institutions
- University Hospital of North Durham (GB)
- Duke Regional Hospital (US)
Publication Details
- Journal
- Cureus
- Published
- 2024-11-05
- DOI
- https://doi.org/10.7759/cureus.73037
- Primary Topic
- Vasculitis and related conditions
- Type
- article
- Field-Weighted Citation Impact
- 0.00