{"title":"Adolescent-onset primary brain calcification: a case report presenting with neuropsychiatric symptoms.","authors":"Yiğit Özaydın, Fevzi Tuna Ocakoğlu, Eyüp Sabri Ercan","doi":"10.1080/13554794.2025.2562920","DOIUrl":null,"url":null,"abstract":"<p><p>Fahr syndrome is a rare neurological condition characterized by idiopathic bilateral basal ganglia calcifications. It often presents psychiatric symptoms that may precede neurological signs, especially in adolescents, making early diagnosis a challenge. We report the case of a 17-year-old male who exhibited treatment-resistant psychotic symptoms including aggression, paranoia, and auditory hallucinations beginning at age 12. Extensive bilateral calcifications in the basal ganglia and subcortical regions were identified via cranial CT, with no evidence of metabolic or infectious etiology, confirming the diagnosis of idiopathic Fahr syndrome. Treatment with clozapine and brexpiprazole led to rapid and sustained symptom remission. This case emphasizes the importance of neuroimaging in adolescents with atypical psychiatric presentations and suggests that combined antipsychotic therapy may be effective in managing Fahr syndrome-related psychosis.</p>","PeriodicalId":49762,"journal":{"name":"Neurocase","volume":" ","pages":"278-284"},"PeriodicalIF":0.5000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurocase","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/13554794.2025.2562920","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/19 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Fahr syndrome is a rare neurological condition characterized by idiopathic bilateral basal ganglia calcifications. It often presents psychiatric symptoms that may precede neurological signs, especially in adolescents, making early diagnosis a challenge. We report the case of a 17-year-old male who exhibited treatment-resistant psychotic symptoms including aggression, paranoia, and auditory hallucinations beginning at age 12. Extensive bilateral calcifications in the basal ganglia and subcortical regions were identified via cranial CT, with no evidence of metabolic or infectious etiology, confirming the diagnosis of idiopathic Fahr syndrome. Treatment with clozapine and brexpiprazole led to rapid and sustained symptom remission. This case emphasizes the importance of neuroimaging in adolescents with atypical psychiatric presentations and suggests that combined antipsychotic therapy may be effective in managing Fahr syndrome-related psychosis.
期刊介绍:
Neurocase is a rapid response journal of case studies and innovative group studies in neuropsychology, neuropsychiatry and behavioral neurology that speak to the neural basis of cognition. Four types of manuscript are considered for publication: single case investigations that bear directly on issues of relevance to theoretical issues or brain-behavior relationships; group studies of subjects with brain dysfunction that address issues relevant to the understanding of human cognition; reviews of important topics in the domains of neuropsychology, neuropsychiatry and behavioral neurology; and brief reports (up to 2500 words) that replicate previous reports dealing with issues of considerable significance. Of particular interest are investigations that include precise anatomical localization of lesions or neural activity via imaging or other techniques, as well as studies of patients with neurodegenerative diseases, since these diseases are becoming more common as our population ages. Topic reviews are included in most issues.