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.

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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
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article

Adrenal neurofibroma masquerading as phaeochromocytoma

Liza Das, Vivek Jha, Amal Shaharyar, Durairaj Arjunan et al.
IJEM Case Reports
Adrenal and Paraganglionic Tumors
article

Adrenal neurofibroma masquerading as phaeochromocytoma

Liza Das, Vivek Jha, Amal Shaharyar, Durairaj Arjunan, Sanjay Kumar Bhadada
article en

Abstract

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.

IJEM Case ReportsVol. 2(4)
Post Graduate Institute of Medical Education and Research (IN)
Openalex Percentile: Top 59%
Adrenal and Paraganglionic Tumors
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Adrenal neurofibroma masquerading as phaeochromocytoma — Liza Das, Vivek Jha, et al. · IJEM Case Reports (2024) | TGRS Research Map | TGRS