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Permanent Cerebral Vessel Occlusion via Double Ligature and Transection
Published on: July 21, 2013
Spontaneous coronary artery dissection in a male patient with haemophilia A: a case report
Mitsukuni Kimura1, Yasuhiro Nakano1, Kotaro Abe1
1Department of Cardiovascular Medicine, Faculty of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Background:
Spontaneous coronary artery dissection (SCAD) is characterized by the unexpected formation of an intramural haemorrhage within the wall of an epicardial coronary artery with or without an intimal tear, resulting in an acute coronary syndrome. Haemophilia A and B are inherited X-linked recessive bleeding disorders caused by the absence or dysfunction of clotting factors VIII (FVIII) or IX.
Case Summary:
A 50-year-old male patient with a history of haemophilia A, type 2 diabetes and smoking presented to our facility with prolonged chest pain. His laboratory results revealed increased myocardial biomarkers and an elevated activated partial thromboplastin time despite the absence of previous bleeding tendencies or coagulation factor replacement therapy. Non-ST-elevation myocardial infarction was suspected, and coronary angiography detected severe stenosis in the left circumflex artery. Intravascular ultrasound confirmed an intramural haematoma without an intimal tear, resulting in an SCAD diagnosis. The patient, with no bleeding complications, was conservatively treated with medications, including aspirin and bisoprolol. A coronary computed tomographic angiography (CCTA) on day 3 revealed haematoma resolution, and the patient was discharged on day 11. CCTA at 8 months detected the disappearance of the previously seen intramural haematoma.
Discussion:
We revealed two important clinical issues: (i) SCAD in a male patient with haemophilia and (ii) the usefulness of CCTA in observing SCAD lesions.
