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Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites
Patient: Male, 43 Final Diagnosis: Splenic aneurysm Symptoms: Ascites • fever • portal hypertension Medication: — Clinical Procedure: — Specialty: Surgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Splenic aneurysms are rare, asymptomatic, and usually derive from previous surgi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280719/ https://www.ncbi.nlm.nih.gov/pubmed/30478253 http://dx.doi.org/10.12659/AJCR.911106 |
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author | Ktenidis, Kiriakos Manaki, Vasiliki Kapoulas, Konstantinos Kourtellari, Eleni Gionis, Michalis |
author_facet | Ktenidis, Kiriakos Manaki, Vasiliki Kapoulas, Konstantinos Kourtellari, Eleni Gionis, Michalis |
author_sort | Ktenidis, Kiriakos |
collection | PubMed |
description | Patient: Male, 43 Final Diagnosis: Splenic aneurysm Symptoms: Ascites • fever • portal hypertension Medication: — Clinical Procedure: — Specialty: Surgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Splenic aneurysms are rare, asymptomatic, and usually derive from previous surgical interventions. Endovascular repair is the best option, but when A-V shunt is present, open repair might be more suitable. CASE REPORT: A 43-year-old man presented to the Internal Medicine Department of AHEPA University Hospital with symptoms of fever and ascites. He was an ex-medical student with a history of sickle cell anemia, who had undergone urgent splenectomy and cholecystectomy 26 years ago and had a transit ischemic attack at the age of 21 years. Diagnostic imaging control revealed a giant splenic aneurysm 9.8 cm in diameter and 5 cm in length, with a concomitant A-V shunt (due to common ligation of the vessels after splenectomy and long stump presence with concomitant erosion of arterial wall). The patient underwent open surgery and cross-clamping the orifice of the splenic artery, also including the splenic vein, and the vessels were ligated. Post-operatively, the patient remained in the Intensive Care Unit for 48 h and suffered a portal vein thrombosis treated with appropriate anticoagulants. One month later, he had acute hemorrhagic pancreatitis and paralytic ileus and underwent laparotomy performed by general surgeons. CONCLUSIONS: Giant splenic aneurysms are rare and are usually caused by previous splenectomy and preservation of a long-vessel stump. Immediate surgical repair is mandatory because of the high risk of rupture. |
format | Online Article Text |
id | pubmed-6280719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62807192019-01-16 Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites Ktenidis, Kiriakos Manaki, Vasiliki Kapoulas, Konstantinos Kourtellari, Eleni Gionis, Michalis Am J Case Rep Articles Patient: Male, 43 Final Diagnosis: Splenic aneurysm Symptoms: Ascites • fever • portal hypertension Medication: — Clinical Procedure: — Specialty: Surgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Splenic aneurysms are rare, asymptomatic, and usually derive from previous surgical interventions. Endovascular repair is the best option, but when A-V shunt is present, open repair might be more suitable. CASE REPORT: A 43-year-old man presented to the Internal Medicine Department of AHEPA University Hospital with symptoms of fever and ascites. He was an ex-medical student with a history of sickle cell anemia, who had undergone urgent splenectomy and cholecystectomy 26 years ago and had a transit ischemic attack at the age of 21 years. Diagnostic imaging control revealed a giant splenic aneurysm 9.8 cm in diameter and 5 cm in length, with a concomitant A-V shunt (due to common ligation of the vessels after splenectomy and long stump presence with concomitant erosion of arterial wall). The patient underwent open surgery and cross-clamping the orifice of the splenic artery, also including the splenic vein, and the vessels were ligated. Post-operatively, the patient remained in the Intensive Care Unit for 48 h and suffered a portal vein thrombosis treated with appropriate anticoagulants. One month later, he had acute hemorrhagic pancreatitis and paralytic ileus and underwent laparotomy performed by general surgeons. CONCLUSIONS: Giant splenic aneurysms are rare and are usually caused by previous splenectomy and preservation of a long-vessel stump. Immediate surgical repair is mandatory because of the high risk of rupture. International Scientific Literature, Inc. 2018-11-27 /pmc/articles/PMC6280719/ /pubmed/30478253 http://dx.doi.org/10.12659/AJCR.911106 Text en © Am J Case Rep, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Ktenidis, Kiriakos Manaki, Vasiliki Kapoulas, Konstantinos Kourtellari, Eleni Gionis, Michalis Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites |
title | Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites |
title_full | Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites |
title_fullStr | Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites |
title_full_unstemmed | Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites |
title_short | Giant Splenic Aneurysm with Arteriovenous (A-V) Shunt, Portal Hypertension, and Ascites |
title_sort | giant splenic aneurysm with arteriovenous (a-v) shunt, portal hypertension, and ascites |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280719/ https://www.ncbi.nlm.nih.gov/pubmed/30478253 http://dx.doi.org/10.12659/AJCR.911106 |
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