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A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy

A 28-year-old woman with a past medical history significant for cervical cancer was diagnosed with a 2.5 cm adrenal tumor but was lost to follow-up. Two years later, she presented to the emergency room with worsening right upper abdominal and flank pain. The computed tomography (CT) and magnetic res...

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Autores principales: Porter, Katherine R, Shroff, Seema, Tran, Tien-Anh, Neychev, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816533/
https://www.ncbi.nlm.nih.gov/pubmed/31667035
http://dx.doi.org/10.7759/cureus.5500
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author Porter, Katherine R
Shroff, Seema
Tran, Tien-Anh
Neychev, Vladimir
author_facet Porter, Katherine R
Shroff, Seema
Tran, Tien-Anh
Neychev, Vladimir
author_sort Porter, Katherine R
collection PubMed
description A 28-year-old woman with a past medical history significant for cervical cancer was diagnosed with a 2.5 cm adrenal tumor but was lost to follow-up. Two years later, she presented to the emergency room with worsening right upper abdominal and flank pain. The computed tomography (CT) and magnetic resonance imaging (MRI) of the abdomen and pelvis revealed that the right adrenal mass had nearly doubled in size (4.3 cm), was heterogeneous with calcifications, central necrosis and actively uptaking the intravenous (IV) contrast with a delayed washout. The biochemical workup was negative for hyperaldosteronism, hypercortisolism, and pheochromocytoma. She reported an unintentional body weight loss of 40 pounds. Adrenocortical carcinoma or a metastatic malignancy was high on the differential diagnoses list. She underwent a successful laparoscopic adrenalectomy, and final pathology revealed a benign extra-adrenal combined ganglioneurofibroma and schwannoma. These rare benign malignancies alone or in combination may closely mimic the clinical and imaging characteristics of adrenal malignancy and pose a diagnostic and therapeutic dilemma to surgeons as well as cause a significant distress to patients and their families. Thus, it is important to thoroughly document and report these cases in order to increase awareness and improve our understanding of the biology, natural history and management of these extremely rare tumors.
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spelling pubmed-68165332019-10-30 A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy Porter, Katherine R Shroff, Seema Tran, Tien-Anh Neychev, Vladimir Cureus General Surgery A 28-year-old woman with a past medical history significant for cervical cancer was diagnosed with a 2.5 cm adrenal tumor but was lost to follow-up. Two years later, she presented to the emergency room with worsening right upper abdominal and flank pain. The computed tomography (CT) and magnetic resonance imaging (MRI) of the abdomen and pelvis revealed that the right adrenal mass had nearly doubled in size (4.3 cm), was heterogeneous with calcifications, central necrosis and actively uptaking the intravenous (IV) contrast with a delayed washout. The biochemical workup was negative for hyperaldosteronism, hypercortisolism, and pheochromocytoma. She reported an unintentional body weight loss of 40 pounds. Adrenocortical carcinoma or a metastatic malignancy was high on the differential diagnoses list. She underwent a successful laparoscopic adrenalectomy, and final pathology revealed a benign extra-adrenal combined ganglioneurofibroma and schwannoma. These rare benign malignancies alone or in combination may closely mimic the clinical and imaging characteristics of adrenal malignancy and pose a diagnostic and therapeutic dilemma to surgeons as well as cause a significant distress to patients and their families. Thus, it is important to thoroughly document and report these cases in order to increase awareness and improve our understanding of the biology, natural history and management of these extremely rare tumors. Cureus 2019-08-27 /pmc/articles/PMC6816533/ /pubmed/31667035 http://dx.doi.org/10.7759/cureus.5500 Text en Copyright © 2019, Porter et al. http://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 General Surgery
Porter, Katherine R
Shroff, Seema
Tran, Tien-Anh
Neychev, Vladimir
A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy
title A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy
title_full A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy
title_fullStr A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy
title_full_unstemmed A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy
title_short A Unique Combined Ganglioneuroma Schwannoma Tumor Mimicking Adrenal Malignancy
title_sort unique combined ganglioneuroma schwannoma tumor mimicking adrenal malignancy
topic General Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816533/
https://www.ncbi.nlm.nih.gov/pubmed/31667035
http://dx.doi.org/10.7759/cureus.5500
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