Adrenal neurofibroma masquerading as phaeochromocytoma
ABSTRACT This study describes the case of a 48-year-old male who was incidentally found to have a left adrenal mass during routine imaging, despite having no significant medical history or symptoms. Initial laboratory tests revealed elevated plasma-free normetanephrines, leading to a preliminary diagnosis of pheochromocytoma (PCC). Imaging confirmed a left large adrenal mass, which suggested PCC. However, following laparoscopic surgical excision, histopathological examination identified the mass as a neurofibroma, an uncommon and benign tumor in the adrenal gland. Post-surgery, the patient’s biochemical markers normalized, and follow-up imaging showed no residual mass. This case underscores the importance of thorough evaluation and consideration of differential diagnoses in the management of adrenal incidentalomas.
Authors
- Liza Das (ORCID: https://orcid.org/0000-0002-9701-9554)
- Vivek Jha (ORCID: https://orcid.org/0000-0002-4144-1107)
- Amal Shaharyar
- Durairaj Arjunan
- Sanjay Kumar Bhadada
Institutions
- Post Graduate Institute of Medical Education and Research (IN)
Publication Details
- Journal
- IJEM Case Reports
- Published
- 2024-10-01
- DOI
- https://doi.org/10.4103/ijemcr.ijemcr_56_24
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00