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Background <p>Differentiating obsessive–compulsive disorder (OCD) from psychotic disorders can be problematic, especially when OCD symptoms present with poor insight and psychotic-like intensity.</p> Case presentation <p>This case report describes a 44-year-old white male, whose symptoms began in his late teens. Clinical documentation, however, began in 2009, when he was first hospitalized. Although he was initially diagnosed with psychosis, his intrusive quasi-delusional fears and compulsions, accompanied by experiences of being watched and abstract ideas about the “ego” with limited insight, led to diagnostic uncertainty. While antipsychotic treatment was ineffective, the initiation of paroxetine in 2011 resulted in substantial improvement, suggesting an OCD etiology. Despite later revision of his diagnosis (after more than 10&#xa0;years following manifestation) toward an OCD spectrum disorder, the patient continued to believe he had psychosis and developed obsessive fears of becoming psychotic, likely influenced by prior clinical labeling.</p> Conclusion <p>This case underscores the importance of careful differential diagnosis in OCD with poor insight. Early recognition of OCD can significantly alter prognosis and treatment course, avoiding prolonged exposures to neuroleptics.</p>

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A fine line between obsessive–compulsive disorder (OCD) and psychotic disorder: a case report

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年7月24日

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  • Natalia Chechko,
  • Stefanie Weisenfeld,
  • Susanne Nehls

摘要

Background

Differentiating obsessive–compulsive disorder (OCD) from psychotic disorders can be problematic, especially when OCD symptoms present with poor insight and psychotic-like intensity.

Case presentation

This case report describes a 44-year-old white male, whose symptoms began in his late teens. Clinical documentation, however, began in 2009, when he was first hospitalized. Although he was initially diagnosed with psychosis, his intrusive quasi-delusional fears and compulsions, accompanied by experiences of being watched and abstract ideas about the “ego” with limited insight, led to diagnostic uncertainty. While antipsychotic treatment was ineffective, the initiation of paroxetine in 2011 resulted in substantial improvement, suggesting an OCD etiology. Despite later revision of his diagnosis (after more than 10 years following manifestation) toward an OCD spectrum disorder, the patient continued to believe he had psychosis and developed obsessive fears of becoming psychotic, likely influenced by prior clinical labeling.

Conclusion

This case underscores the importance of careful differential diagnosis in OCD with poor insight. Early recognition of OCD can significantly alter prognosis and treatment course, avoiding prolonged exposures to neuroleptics.