Uncommon Adrenal Tumors: A Case Series

Guddi Rani Singh

Department of Pathology, IGIMS, Patna, Bihar, India.

Richa Sharma

Department of Pathology, IGIMS, Patna, Bihar, India.

Anand Kumar

Department of Endocrinology and Metabolism, IGIMS, Patna, Bihar, India

Deepak Kumar

Department of Radiodiagnosis, IGIMS, Patna, Bihar, India.

Rakesh Kumar Singh

Department of Surgical Gastroenterology and Liver Transplant, IGIMS, Patna, Bihar, India.

Mamta Kumari *

Department of Pathology, IGIMS, Patna, Bihar, India.

*Author to whom correspondence should be addressed.


Abstract

Adrenal tumors are very rare. These lesions are called adrenal incidentalomas because they are incidentally detected through imaging procedure. Its prevalence ranges from 1.4% to 2.9% worldwide. Clinical suspicion, laboratory testing, Imaging and histopathological examination needed for definite diagnosis. We report three cases of adrenal tumors received at our institute between the year 2021 and 2022. Pheochromocytoma of Adrenal gland scaled score (PASS) tells about the prognosis based on histopathological findings. Earliest management is essential as these tumors are related with secretion of hormones and may have a poor prognosis.

Keywords: Incidentalomas, management, hormones, prognosis


How to Cite

Rani Singh, Guddi, Richa Sharma, Anand Kumar, Deepak Kumar, Rakesh Kumar Singh, and Mamta Kumari. 2022. “Uncommon Adrenal Tumors: A Case Series”. Journal of Advances in Medicine and Medical Research 34 (24):299-303. https://doi.org/10.9734/jammr/2022/v34i244943.

Downloads

Download data is not yet available.