Characteristics of Bilateral Adrenal Lesions: Experience from an Indian Tertiary Care Centre

• Published in: Indian journal of endocrinology and metabolism Vol. 28; no. 3; pp. 273 - 278
• Main Authors: Niranjan, Gauri, Prasad, Pallavi, Gupta, Neelima, Agrawal, Vinita, Mishra, Anjali, Jain, Neeraj, Kapoor, Vishwas
• Format: Journal Article
• Language: English
• Published: India Medknow Publications & Media Pvt. Ltd 01-05-2024; Wolters Kluwer - Medknow; Wolters Kluwer Medknow Publications
• Subjects: adrenal; bilateral; Etiology; histoplasmosis; Hyperplasia; hypocortisolism; infection; Original; pheochromocytoma; Tumors; infection; bilateral; hypocortisolism; pheochromocytoma; hyperplasia; histoplasmosis; Adrenal
• ISSN: 2230-8210; 2230-9500
• DOI: 10.4103/ijem.ijem_232_23

The aetiologies in unilateral and bilateral adrenal lesions can be different with different clinical implications and management guidelines, the latter having aetiologies like hyperplasia, infections, infiltrative lesions and neoplasia. Bilateral tumours are more likely to have hereditary/syndromic associations. There is limited data on the clinical and pathological profile of bilateral adrenal lesions.
This was a retrospective study where patients with bilateral adrenal lesions were selected from a total of 266 patients with adrenal lesions who presented to our institute between January 2016 and August 2022. The demographic, laboratory and imaging data were retrieved from the Hospital Information System and patient case files.
The study included 51 patients; the mean age at presentation was 51.15 years (range 14 to 82 years). Forty-eight patients (94.1%) were symptomatic at presentation with an average duration of symptoms being 10.68 months (range 10 days to 1 year). The most common presentation was adrenal insufficiency in 18 cases (38%), followed by fever in 17 cases (36%). The commonest aetiology, as revealed on histopathology, was histoplasmosis (
= 22, 43%), followed by pheochromocytoma (
= 11, 21.5%), metastases (
= 6, 11.7%), adrenal hyperplasia (
= 5, 9.8%), adrenocortical adenoma (
= 1, 1.9%), lymphoma (
= 3, 5.8%), neuroblastoma (
= 1, 1.9%), myelolipoma (
= 1, 1.9%) and tuberculosis (
= 1, 1.9%). Histoplasmosis and metastatic lesions were commonly seen in older people, and pheochromocytoma was associated with young age. 6/11 patients with a diagnosis of bilateral pheochromocytoma were associated with family history, genetic mutation and extra-adrenal involvement.
The approach to bilateral adrenal lesions differs from that of unilateral lesions due to differences in aetiologies and the more significant role of genetics in some bilateral tumours. The age at presentation, presenting symptoms, lesion size and biochemical features help delineate varied underlying aetiologies.