Delayed diagnosis and long-term complications of pheochromocytoma: a case study on the challenges of rare disease management
Abstract The delayed diagnosis and frequent misdiagnoses of rare diseases exacerbate the challenges faced by patients, with adolescents and females experiencing the longest delays. Children with rare conditions often grapple with social isolation, stigma, and academic setbacks, while adults encounte...
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| Main Author: | |
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| Format: | Article |
| Language: | English |
| Published: |
Springer
2025-08-01
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| Series: | Journal of Rare Diseases |
| Subjects: | |
| Online Access: | https://doi.org/10.1007/s44162-025-00098-7 |
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| Summary: | Abstract The delayed diagnosis and frequent misdiagnoses of rare diseases exacerbate the challenges faced by patients, with adolescents and females experiencing the longest delays. Children with rare conditions often grapple with social isolation, stigma, and academic setbacks, while adults encounter career disruptions, strained relationships, and workplace stigma. This paper presents a case study of a patient diagnosed with pheochromocytoma after prolonged symptoms, highlighting the medical, emotional, and social challenges of navigating a rare disease. Her experiences underscore the effects of misdiagnoses, inadequate provider communication, and unmet expectations regarding treatment outcomes. The transition of care for pediatric patients with rare diseases and the importance of building trust between patients and providers are also explored. Future directions include enhancing provider awareness, fostering multidisciplinary care, and improving transitions between pediatric and adult healthcare. These strategies aim to create a more empathetic and effective care environment, empowering patients to manage the complexities of their conditions while maintaining trust in the healthcare system. |
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| ISSN: | 2731-085X |