{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,14]],"date-time":"2025-05-14T02:37:07Z","timestamp":1747190227137,"version":"3.40.5"},"reference-count":10,"publisher":"Wiley","license":[{"start":{"date-parts":[[2020,3,4]],"date-time":"2020-03-04T00:00:00Z","timestamp":1583280000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Hematology"],"published-print":{"date-parts":[[2020,3,4]]},"abstract":"<jats:p>Atypical hemolytic uremic syndrome (aHUS) is a thrombotic microangiopathy (TMA)-related disease that manifests as a triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury (AKI) and is caused by uncontrolled activation of the complement system. We report the case of a 61-year-old woman with acute type A aortic dissection that subsequently developed into aHUS. The hematologic disorders underlying aHUS improved after treatment with the complement inhibitor eculizumab. It is important to consider aHUS when a patient clinically develops a triad of microangiopathic hemolytic anemia, thrombocytopenia, and an increasing creatinine level following cardiovascular surgery.<\/jats:p>","DOI":"10.1155\/2020\/2467953","type":"journal-article","created":{"date-parts":[[2020,3,4]],"date-time":"2020-03-04T23:31:55Z","timestamp":1583364715000},"page":"1-4","source":"Crossref","is-referenced-by-count":3,"title":["Atypical Hemolytic Uremic Syndrome following Acute Type A Aortic Dissection"],"prefix":"10.1155","volume":"2020","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6547-9513","authenticated-orcid":true,"given":"Eigo","family":"Ikushima","sequence":"first","affiliation":[{"name":"Department of Cardiovascular Surgery, Japan Community Healthcare Organization (JCHO) Kyushu Hospital, 1-8-1, Kishinoura, Yahatanishi-ku, Kitakyushu, Fukuoka 806-8501, 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