Department of Psychiatry, Creighton University School of Medicine, Phoenix, AZ, USA.
Department of Psychiatry, University of Southern California, Los Angeles, CA, USA.
BMC Psychiatry. 2024 Oct 24;24(1):730. doi: 10.1186/s12888-024-06180-6.
Pediatric autoimmune neuropsychiatric disorders associated with streptococcus (PANDAS) is a controversial diagnosis with limited evidence-based treatment guidelines available, particularly for severe and treatment-resistant cases.
This report describes a 9-year-old male presenting with sudden onset, severe obsessive-compulsive disorder (OCD) symptoms one month following a streptococcus infection. His symptoms included suicidality and recurrent self-injurious behaviors, which led to multiple inpatient hospitalizations. He was diagnosed with PANDAS and was treated with psychotropic medications, antibiotics, immunotherapy, and a tonsillectomy. Over the two years since initial admission, the patient's condition improved, with a decrease in symptom severity and an increase in adaptive functioning, though symptom remission was slow to occur.
This paper explores the controversies surrounding the PANDAS diagnosis, reviews potential treatments, and discusses the dilemmas of medical decision-making in the setting of severe treatment-resistant symptoms and limited evidence-based guidelines. We hope that this case report will be valuable to healthcare providers facing similar presentations and inspire further investigation into this complex condition.
与链球菌相关的儿科自身免疫性神经精神障碍(PANDAS)是一种存在争议的诊断,其治疗指南有限,特别是对于严重和治疗抵抗的病例。
本报告描述了一名 9 岁男性,在链球菌感染一个月后突然出现严重的强迫症(OCD)症状。他的症状包括自杀意念和反复的自残行为,导致多次住院治疗。他被诊断为 PANDAS,并接受了精神药物、抗生素、免疫疗法和扁桃体切除术治疗。自最初入院以来的两年中,患者的病情有所改善,症状严重程度减轻,适应功能增强,但症状缓解缓慢。
本文探讨了 PANDAS 诊断的争议,回顾了潜在的治疗方法,并讨论了在严重治疗抵抗症状和有限的基于证据的指南的情况下,医疗决策的困境。我们希望本病例报告对面临类似表现的医疗保健提供者具有价值,并激发对这种复杂疾病的进一步研究。