| Literature DB >> 33090364 |
Makoto Toyoda1, Tadashi Kitamura2, Kouki Nakashima3, Yoshikiyo Matsunaga3, Masaki Nie3, Kagami Miyaji2.
Abstract
Sickle cell trait (SCT), a benign hematological condition affecting approximately 300 million individuals globally, is associated with an increased risk of vaso-occlusive disease. However, the risks related to surgery employing cardiopulmonary bypass in patients with SCT are not well established. Herein, we report the case of a 27-year-old African American man with SCT who underwent an emergency aortic repair for acute Stanford type A aortic dissection using hypothermic circulatory arrest. The patient developed a sickle cell crisis, which was followed by spontaneous splenic infarction and rupture, nonocclusive mesenteric ischemia, and spinal infarction.Entities:
Keywords: Aortic dissection; Mesenteric ischemia; Sickle cell trait; Spinal infarction; Splenic rupture
Mesh:
Year: 2020 PMID: 33090364 PMCID: PMC7900333 DOI: 10.1007/s11748-020-01520-1
Source DB: PubMed Journal: Gen Thorac Cardiovasc Surg ISSN: 1863-6705