Cargando…

Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma

A 59-year-old woman underwent an abdominal and pelvic computed tomography (CT) scan to rule out non-obstructive urolithiasis. The patient was asymptomatic, with the exception of occasional bilateral low back pain. A physical examination did not reveal any notable findings. The CT scan revealed the p...

Descripción completa

Detalles Bibliográficos
Autores principales: Giesteira, Bruno, Sousa, Jessica, Pinheiro Amorim, João
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686665/
https://www.ncbi.nlm.nih.gov/pubmed/38034194
http://dx.doi.org/10.7759/cureus.47994
_version_ 1785151817204629504
author Giesteira, Bruno
Sousa, Jessica
Pinheiro Amorim, João
author_facet Giesteira, Bruno
Sousa, Jessica
Pinheiro Amorim, João
author_sort Giesteira, Bruno
collection PubMed
description A 59-year-old woman underwent an abdominal and pelvic computed tomography (CT) scan to rule out non-obstructive urolithiasis. The patient was asymptomatic, with the exception of occasional bilateral low back pain. A physical examination did not reveal any notable findings. The CT scan revealed the presence of an incidental solid left adrenal lesion, which displaced the body of the pancreas and the left kidney. The lesion measured 7 cm × 6.5 cm and exhibited a rounded morphology with well-defined margins. It showed progressive and heterogeneous contrast uptake. Additionally, magnetic resonance imaging (MRI) was performed, confirming the presence of an adrenal lesion with intense and heterogeneous hypersignal on T2. The lesion also demonstrated heterogeneous and persistent enhancement in a dynamic study. Furthermore, there were some indistinct and non-specific hypointense areas identified on both T1 and T2 sequences. The lesion exhibited moderately restricted diffusion. Although the imaging features were non-specific, there were no indications of invasion or distant metastasis, which made a benign large adrenal mass the most likely diagnosis. Non-functioning pheochromocytoma, lipid-poor adrenal adenoma, as well as metastasis or primary adrenal carcinoma, were considered differential diagnoses. The patient underwent an elective adrenalectomy, during which the identified lesion was completely resected. The patient's postoperative recovery was uneventful, and she was discharged three days after the procedure. Subsequent histopathological evaluation revealed an oncocytic neoplasm of the adrenal cortex - specifically, an oncocytoma.
format Online
Article
Text
id pubmed-10686665
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cureus
record_format MEDLINE/PubMed
spelling pubmed-106866652023-11-30 Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma Giesteira, Bruno Sousa, Jessica Pinheiro Amorim, João Cureus Radiology A 59-year-old woman underwent an abdominal and pelvic computed tomography (CT) scan to rule out non-obstructive urolithiasis. The patient was asymptomatic, with the exception of occasional bilateral low back pain. A physical examination did not reveal any notable findings. The CT scan revealed the presence of an incidental solid left adrenal lesion, which displaced the body of the pancreas and the left kidney. The lesion measured 7 cm × 6.5 cm and exhibited a rounded morphology with well-defined margins. It showed progressive and heterogeneous contrast uptake. Additionally, magnetic resonance imaging (MRI) was performed, confirming the presence of an adrenal lesion with intense and heterogeneous hypersignal on T2. The lesion also demonstrated heterogeneous and persistent enhancement in a dynamic study. Furthermore, there were some indistinct and non-specific hypointense areas identified on both T1 and T2 sequences. The lesion exhibited moderately restricted diffusion. Although the imaging features were non-specific, there were no indications of invasion or distant metastasis, which made a benign large adrenal mass the most likely diagnosis. Non-functioning pheochromocytoma, lipid-poor adrenal adenoma, as well as metastasis or primary adrenal carcinoma, were considered differential diagnoses. The patient underwent an elective adrenalectomy, during which the identified lesion was completely resected. The patient's postoperative recovery was uneventful, and she was discharged three days after the procedure. Subsequent histopathological evaluation revealed an oncocytic neoplasm of the adrenal cortex - specifically, an oncocytoma. Cureus 2023-10-30 /pmc/articles/PMC10686665/ /pubmed/38034194 http://dx.doi.org/10.7759/cureus.47994 Text en Copyright © 2023, Giesteira et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Radiology
Giesteira, Bruno
Sousa, Jessica
Pinheiro Amorim, João
Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma
title Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma
title_full Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma
title_fullStr Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma
title_full_unstemmed Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma
title_short Incidental Adrenal Masses: A Case Report of an Adrenal Oncocytoma
title_sort incidental adrenal masses: a case report of an adrenal oncocytoma
topic Radiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686665/
https://www.ncbi.nlm.nih.gov/pubmed/38034194
http://dx.doi.org/10.7759/cureus.47994
work_keys_str_mv AT giesteirabruno incidentaladrenalmassesacasereportofanadrenaloncocytoma
AT sousajessica incidentaladrenalmassesacasereportofanadrenaloncocytoma
AT pinheiroamorimjoao incidentaladrenalmassesacasereportofanadrenaloncocytoma