Demographics, Clinical Profiles, and Outcomes of Patients With Adrenal Disorders in a Tertiary Care Center: A Retrospective Study
This study highlights a high prevalence of pheochromocytoma and incidentalomas in our cohort, with effective multidisciplinary management yielding favorable outcomes. Increased size showed increased malignancy risk, supporting surgical intervention thresholds. Complex cases underscore the need for tailored approaches. Enhanced hormonal testing, genetic screening, and longer follow-up are recommended to improve care in resource-limited settings.
Authors
- Arif Hamid (ORCID: https://orcid.org/0000-0001-7403-0067)
- Tabassum Khan (ORCID: https://orcid.org/0000-0002-3723-0833)
- Abdul Rouf Khawaja (ORCID: https://orcid.org/0000-0002-6799-0462)
- Firdous Ahmad Beigh
- Sajad Ahmad Malik (ORCID: https://orcid.org/0000-0001-5540-7607)
- S K Verma (ORCID: https://orcid.org/0000-0001-6954-9315)
- Saqib Mehdi (ORCID: https://orcid.org/0000-0002-0938-9054)
- Sajjad A Para
- Mudasir Ahmad Tantray
Institutions
- Sher-i-Kashmir Institute of Medical Sciences (IN)
Publication Details
- Journal
- Cureus
- Published
- 2025-09-15
- DOI
- https://doi.org/10.7759/cureus.92389
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00