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23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst

INTRODUCTION: Splenic cysts are rare. They are usually incidentally diagnosed and there is no harmonised treatment pathway. We report a case of a large splenic epidermoid type cyst without history of previous abdominal trauma. PRESENTATION OF CASE: A 23-year old male patient presented with symptoms...

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Autores principales: Senn, Alina Samia, Bauer, Robert Christian, Heigl, Andres, Rosenberg, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976122/
https://www.ncbi.nlm.nih.gov/pubmed/35367949
http://dx.doi.org/10.1016/j.ijscr.2022.106991
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author Senn, Alina Samia
Bauer, Robert Christian
Heigl, Andres
Rosenberg, Robert
author_facet Senn, Alina Samia
Bauer, Robert Christian
Heigl, Andres
Rosenberg, Robert
author_sort Senn, Alina Samia
collection PubMed
description INTRODUCTION: Splenic cysts are rare. They are usually incidentally diagnosed and there is no harmonised treatment pathway. We report a case of a large splenic epidermoid type cyst without history of previous abdominal trauma. PRESENTATION OF CASE: A 23-year old male patient presented with symptoms of upper abdominal pain, nausea and vomiting. Except for a tenderness in the upper and lower left quadrant of the abdomen, the initial examination showed no extraordinary findings. A contrast enhanced computed tomography revealed a large singular splenic cyst displacing neighbouring structures. Echinococcus serology was tested negative. A laparoscopic fenestration of the superficially located splenic cyst was performed. Perioperative course was free of complications. Histopathological analysis of the excisate showed a squamous lining indicating the cyst as epidermoid type. DISCUSSION: Non-parasitic cyst types include traumatic, neoplastic, degenerative and congenital cysts. Due to its considerable size, our patients splenic cyst was diagnosed after occurring symptoms lead to further examination (CT scan). Laparoscopic fenestration of the cyst was chosen as the optimal surgical approach because of the superficial location of the cyst and to preserve residual splenic parenchyma. In the present case, recurrence of the splenic cyst appeared, which left the patient with a total splenectomy as the final treatment choice. CONCLUSION: Due to the unspecific symptoms, the diagnosis of a splenic cyst can be prolonged. Choosing the adequate surgical technique to avoid complications is crucial. By deepening the understanding of the condition and surgical approaches, we can improve diagnostic and therapeutic management for affected patients.
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spelling pubmed-89761222022-04-03 23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst Senn, Alina Samia Bauer, Robert Christian Heigl, Andres Rosenberg, Robert Int J Surg Case Rep Case Report INTRODUCTION: Splenic cysts are rare. They are usually incidentally diagnosed and there is no harmonised treatment pathway. We report a case of a large splenic epidermoid type cyst without history of previous abdominal trauma. PRESENTATION OF CASE: A 23-year old male patient presented with symptoms of upper abdominal pain, nausea and vomiting. Except for a tenderness in the upper and lower left quadrant of the abdomen, the initial examination showed no extraordinary findings. A contrast enhanced computed tomography revealed a large singular splenic cyst displacing neighbouring structures. Echinococcus serology was tested negative. A laparoscopic fenestration of the superficially located splenic cyst was performed. Perioperative course was free of complications. Histopathological analysis of the excisate showed a squamous lining indicating the cyst as epidermoid type. DISCUSSION: Non-parasitic cyst types include traumatic, neoplastic, degenerative and congenital cysts. Due to its considerable size, our patients splenic cyst was diagnosed after occurring symptoms lead to further examination (CT scan). Laparoscopic fenestration of the cyst was chosen as the optimal surgical approach because of the superficial location of the cyst and to preserve residual splenic parenchyma. In the present case, recurrence of the splenic cyst appeared, which left the patient with a total splenectomy as the final treatment choice. CONCLUSION: Due to the unspecific symptoms, the diagnosis of a splenic cyst can be prolonged. Choosing the adequate surgical technique to avoid complications is crucial. By deepening the understanding of the condition and surgical approaches, we can improve diagnostic and therapeutic management for affected patients. Elsevier 2022-03-29 /pmc/articles/PMC8976122/ /pubmed/35367949 http://dx.doi.org/10.1016/j.ijscr.2022.106991 Text en © 2022 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Senn, Alina Samia
Bauer, Robert Christian
Heigl, Andres
Rosenberg, Robert
23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst
title 23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst
title_full 23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst
title_fullStr 23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst
title_full_unstemmed 23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst
title_short 23-year old man with a long history of abdominal pain, nausea and vomiting: Case report of a splenic cyst
title_sort 23-year old man with a long history of abdominal pain, nausea and vomiting: case report of a splenic cyst
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976122/
https://www.ncbi.nlm.nih.gov/pubmed/35367949
http://dx.doi.org/10.1016/j.ijscr.2022.106991
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