Neurofibroma of Adrenal gland- A rare case report


Case Report

Author Details : Ankita N*, Nagarekha K, M Shanthi, Patil Shashirekha

Volume : 8, Issue : 2, Year : 2023

Article Page : 102-104

https://doi.org/10.18231/j.jdpo.2023.022



Suggest article by email

Get Permission

Abstract

Neurofibroma of the adrenal glands is rare, most common site of presentation are head and neck region and along the nerves. With the us of computed tomography , magnetic resonance imaging , an ultrasonography for the detection of adrenals masses is increasing. On computed tomography neurogenic tumours frequently appear as a distinct, smooth or lobulated mass. All varieties of neurogenic tumours may exhibit calcification But for confirmation of the lesion histopathological examination and immunohistochemistry is a must. Neurofibroma of adrenals although rare but a possibility.
Immunohistochemistry plays an important role in confirming the diagnosis. IHC helps in definitive diagnosis which helps clinicians with management of the patient.

Keywords: Neurofibroma, Adrenal Gland, S­ 100


How to cite : Ankita N, Nagarekha K, Shanthi M, Shashirekha P, Neurofibroma of Adrenal gland- A rare case report. IP J Diagn Pathol Oncol 2023;8(2):102-104


This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.







Article History

Received : 10-03-2023

Accepted : 20-05-2023


View Article

PDF File   Full Text Article


Copyright permission

Get article permission for commercial use

Downlaod

PDF File   XML File   ePub File


Digital Object Identifier (DOI)

Article DOI

https://doi.org/10.18231/j.jdpo.2023.022


Article Metrics






Article Access statistics

Viewed: 700

PDF Downloaded: 590