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A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report

INTRODUCTION: Adrenal pseudocysts are rare cystic masses that arise from the adrenal gland and which are usually non-functional and asymptomatic. Adrenal pseudocysts consist of a fibrous wall without an epithelial or endothelial lining. We report the case of a patient with a giant adrenal pseudocyst...

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Autores principales: Momiyama, Masashi, Matsuo, Kenichi, Yoshida, Kenichi, Tanaka, Kuniya, Akiyama, Hirotoshi, Yamanaka, Shoji, Endo, Itaru
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079673/
https://www.ncbi.nlm.nih.gov/pubmed/21463528
http://dx.doi.org/10.1186/1752-1947-5-135
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author Momiyama, Masashi
Matsuo, Kenichi
Yoshida, Kenichi
Tanaka, Kuniya
Akiyama, Hirotoshi
Yamanaka, Shoji
Endo, Itaru
author_facet Momiyama, Masashi
Matsuo, Kenichi
Yoshida, Kenichi
Tanaka, Kuniya
Akiyama, Hirotoshi
Yamanaka, Shoji
Endo, Itaru
author_sort Momiyama, Masashi
collection PubMed
description INTRODUCTION: Adrenal pseudocysts are rare cystic masses that arise from the adrenal gland and which are usually non-functional and asymptomatic. Adrenal pseudocysts consist of a fibrous wall without an epithelial or endothelial lining. We report the case of a patient with a giant adrenal pseudocyst presenting with right hypochondralgia and high fever. CASE PRESENTATION: A 52-year-old Japanese man was admitted with right hypochondralgia and a chill. Abdominal computed tomography revealed a well-defined cystic mass measuring 19 cm which was located in the right adrenal region and the contents of which were not enhanced with contrast medium. Abdominal ultrasonography revealed a heterogeneously hypo-echoic lesion with a peripheral high-echoic rim. Serum hormonal levels were almost normal. Despite treatment with antibiotics, the high fever persisted. Based on these findings, we made a preoperative diagnosis of a right adrenal cyst with infection. However, the possibility of malignancy still remained. The patient underwent laparotomy and right adrenal cyst excision with partial hepatectomy in order to relieve the symptoms and to confirm an accurate diagnosis. Histological examination revealed an adrenal pseudocyst with infection. His condition improved soon after the operation. CONCLUSION: We report a case of a giant adrenal pseudocyst with infection. Surgery is required for symptomatic cases in order to relieve the symptoms and in cases of uncertain diagnosis.
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spelling pubmed-30796732011-04-20 A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report Momiyama, Masashi Matsuo, Kenichi Yoshida, Kenichi Tanaka, Kuniya Akiyama, Hirotoshi Yamanaka, Shoji Endo, Itaru J Med Case Reports Case Report INTRODUCTION: Adrenal pseudocysts are rare cystic masses that arise from the adrenal gland and which are usually non-functional and asymptomatic. Adrenal pseudocysts consist of a fibrous wall without an epithelial or endothelial lining. We report the case of a patient with a giant adrenal pseudocyst presenting with right hypochondralgia and high fever. CASE PRESENTATION: A 52-year-old Japanese man was admitted with right hypochondralgia and a chill. Abdominal computed tomography revealed a well-defined cystic mass measuring 19 cm which was located in the right adrenal region and the contents of which were not enhanced with contrast medium. Abdominal ultrasonography revealed a heterogeneously hypo-echoic lesion with a peripheral high-echoic rim. Serum hormonal levels were almost normal. Despite treatment with antibiotics, the high fever persisted. Based on these findings, we made a preoperative diagnosis of a right adrenal cyst with infection. However, the possibility of malignancy still remained. The patient underwent laparotomy and right adrenal cyst excision with partial hepatectomy in order to relieve the symptoms and to confirm an accurate diagnosis. Histological examination revealed an adrenal pseudocyst with infection. His condition improved soon after the operation. CONCLUSION: We report a case of a giant adrenal pseudocyst with infection. Surgery is required for symptomatic cases in order to relieve the symptoms and in cases of uncertain diagnosis. BioMed Central 2011-04-04 /pmc/articles/PMC3079673/ /pubmed/21463528 http://dx.doi.org/10.1186/1752-1947-5-135 Text en Copyright ©2011 Momiyama et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Momiyama, Masashi
Matsuo, Kenichi
Yoshida, Kenichi
Tanaka, Kuniya
Akiyama, Hirotoshi
Yamanaka, Shoji
Endo, Itaru
A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
title A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
title_full A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
title_fullStr A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
title_full_unstemmed A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
title_short A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
title_sort giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3079673/
https://www.ncbi.nlm.nih.gov/pubmed/21463528
http://dx.doi.org/10.1186/1752-1947-5-135
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