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Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis
BACKGROUND: Hereditary spherocytosis is a genetic, frequently familial hemolytic blood disease characterized by varying degrees of hemolytic anemia, splenomegaly, and jaundice. There are few reports on adult open-heart surgery for patients with hereditary spherocytosis. CASE PRESENTATION: We report...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002123/ https://www.ncbi.nlm.nih.gov/pubmed/27566068 http://dx.doi.org/10.1186/s13019-016-0534-8 |
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author | Matsuzaki, Yuichi Tomioka, Hideyuki Saso, Masaki Azuma, Takashi Saito, Satoshi Aomi, Shigeyuki Yamazaki, Kenji |
author_facet | Matsuzaki, Yuichi Tomioka, Hideyuki Saso, Masaki Azuma, Takashi Saito, Satoshi Aomi, Shigeyuki Yamazaki, Kenji |
author_sort | Matsuzaki, Yuichi |
collection | PubMed |
description | BACKGROUND: Hereditary spherocytosis is a genetic, frequently familial hemolytic blood disease characterized by varying degrees of hemolytic anemia, splenomegaly, and jaundice. There are few reports on adult open-heart surgery for patients with hereditary spherocytosis. CASE PRESENTATION: We report a rare case of an adult open-heart surgery associated with hereditary spherocytosis. A 63-year-old man was admitted for congestive heart failure due to bicuspid aortic valve, aortic valve regurgitation, and sinus of subaortic aneurysm. The family history, the microscopic findings of the blood smear, and the characteristic osmotic fragility confirmed the diagnosis of hereditary spherocytosis. Furthermore, splenectomy had not been undertaken preoperatively. The patient underwent a successful operation by means of a centrifugal pump. Haptoglobin was used during the cardiopulmonary bypass, and a biological valve was selected to prevent hemolysis. No significant hemolysis occurred intraoperatively or postoperatively. CONCLUSION: There are no previous reports of patients with hereditary spherocytosis, and bicuspid aortic valve. We have successfully performed an adult open-heart surgery using a centrifugal pump in an adult patient suffering from hereditary spherocytosis and bicuspid aortic valve. |
format | Online Article Text |
id | pubmed-5002123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50021232016-08-28 Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis Matsuzaki, Yuichi Tomioka, Hideyuki Saso, Masaki Azuma, Takashi Saito, Satoshi Aomi, Shigeyuki Yamazaki, Kenji J Cardiothorac Surg Case Report BACKGROUND: Hereditary spherocytosis is a genetic, frequently familial hemolytic blood disease characterized by varying degrees of hemolytic anemia, splenomegaly, and jaundice. There are few reports on adult open-heart surgery for patients with hereditary spherocytosis. CASE PRESENTATION: We report a rare case of an adult open-heart surgery associated with hereditary spherocytosis. A 63-year-old man was admitted for congestive heart failure due to bicuspid aortic valve, aortic valve regurgitation, and sinus of subaortic aneurysm. The family history, the microscopic findings of the blood smear, and the characteristic osmotic fragility confirmed the diagnosis of hereditary spherocytosis. Furthermore, splenectomy had not been undertaken preoperatively. The patient underwent a successful operation by means of a centrifugal pump. Haptoglobin was used during the cardiopulmonary bypass, and a biological valve was selected to prevent hemolysis. No significant hemolysis occurred intraoperatively or postoperatively. CONCLUSION: There are no previous reports of patients with hereditary spherocytosis, and bicuspid aortic valve. We have successfully performed an adult open-heart surgery using a centrifugal pump in an adult patient suffering from hereditary spherocytosis and bicuspid aortic valve. BioMed Central 2016-08-26 /pmc/articles/PMC5002123/ /pubmed/27566068 http://dx.doi.org/10.1186/s13019-016-0534-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Matsuzaki, Yuichi Tomioka, Hideyuki Saso, Masaki Azuma, Takashi Saito, Satoshi Aomi, Shigeyuki Yamazaki, Kenji Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
title | Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
title_full | Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
title_fullStr | Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
title_full_unstemmed | Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
title_short | Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
title_sort | open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002123/ https://www.ncbi.nlm.nih.gov/pubmed/27566068 http://dx.doi.org/10.1186/s13019-016-0534-8 |
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