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Adult ALCAPA: from histological picture to clinical features.
Kubota, Hiroshi; Endo, Hidehito; Ishii, Hikaru; Tsuchiya, Hiroshi; Inaba, Yusuke; Terakawa, Katsunari; Takahashi, Yu; Noma, Mio; Takemoto, Kazuya; Taniai, Seiichi; Sakata, Konomi; Soejima, Kyoko; Shimoyamada, Hiroaki; Kamma, Hiroshi; Kawakami, Hayato; Kaneko, Yukihiro; Hirono, Satoru; Izumi, Daisuke; Ozaki, Kazuyuki; Minamino, Tohru; Yoshino, Hideaki; Sudo, Kenichi.
Affiliation
  • Kubota H; Department of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan. kub@ks.kyorin-u.ac.jp.
  • Endo H; Department of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
  • Ishii H; Department of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
  • Tsuchiya H; Department of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
  • Inaba Y; Department of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
  • Terakawa K; Department of Cardiac Surgery, University of Tokyo, Tokyo, Japan.
  • Takahashi Y; Department of Cardiovascular Surgery, National Disaster Medical Center, Tachikawa, Japan.
  • Noma M; Department of Cardiovascular Surgery, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan.
  • Takemoto K; Department of Internal Medicine, Jyukoukai Hospital, Miyoshi, Japan.
  • Taniai S; Department of Cardiology, Kyorin University, Mitaka, Japan.
  • Sakata K; Department of Cardiology, Kyorin University, Mitaka, Japan.
  • Soejima K; Department of Cardiology, Kyorin University, Mitaka, Japan.
  • Shimoyamada H; Department of Pathology, Kyorin University, Mitaka, Japan.
  • Kamma H; Department of Pathology, Kyorin University, Mitaka, Japan.
  • Kawakami H; Department of Anatomy, Kyorin University, Mitaka, Japan.
  • Kaneko Y; Department of Cardiovascular Surgery, National Center for Child Health and Development, Tokyo, Japan.
  • Hirono S; Department of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Izumi D; Department of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Ozaki K; Department of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Minamino T; Department of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Yoshino H; Jiseikai Nomura Hospital, Mitaka, Japan.
  • Sudo K; Jiseikai Nomura Hospital, Mitaka, Japan.
J Cardiothorac Surg ; 15(1): 14, 2020 Jan 13.
Article in En | MEDLINE | ID: mdl-31931842
ABSTRACT

BACKGROUND:

Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital coronary anomaly that results in high mortality if left untreated. Our aim was to extend our knowledge of the histological, angiographic, and clinical characteristics of ALCAPA in order to deepen our understanding of this rare entity. CASE PRESENTATION We were involved in the assessment, treatment, and pathological evaluation of two adult ALCAPA patients who were rescued from ventricular fibrillation and then surgically treated to establish a dual coronary artery system. Histological studies indicated various chronic ischemic changes in the myocardium, patchy fibrosis, and severely thickened arteriolar walls in both ventricles. The first patient is alive and well 11.5 years after surgical correction without any implantable cardioverter defibrillator (ICD) activations. The second patient required re-do surgery 9 months after the initial operation but subsequently died. Histologically, chronic ischemic alteration of the myocardium and thickened arteriolar walls persisted even after surgical correction, and coronary angiography (CAG) showed an extremely slow flow phenomenon even after surgical correction in both patients. The average postoperative opacification rate in the first case was 7.36 + 1.12 (n = 2) in the RCA, 3.81 + 0.51 (n = 3) in the left anterior descending (LAD) artery, and 4.08 + 0.27 (n = 4) in the left circumflex (LCx) artery. The slow flow phenomenon may represent persistent high arteriolar resistance in both ventricles.

CONCLUSIONS:

Seldom reported or new findings in adult ALCAPA were identified in two cases. More frequent diagnosis of adult ALCAPA can be expected because of the widespread availability of resuscitation and more advanced diagnostic modalities. Accumulation of pathological and clinical findings and confirmation of the long-term follow-up results after treatment may contribute to expanding our knowledge of this rare entity and establishing optimal treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bland White Garland Syndrome / Anomalous Left Coronary Artery Type of study: Prognostic_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: J Cardiothorac Surg Year: 2020 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bland White Garland Syndrome / Anomalous Left Coronary Artery Type of study: Prognostic_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: J Cardiothorac Surg Year: 2020 Document type: Article Affiliation country: Japón