Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-26T10:07:13.476Z Has data issue: false hasContentIssue false
  • English
  • Français

Concurrent right atrial isomerism, complete atrioventricular septal defect, and single ventricle in an L-transposition of great arteries patient complicated by brain abscess

Part of: Cardiac Morphology Functionally Univentricular Heart

Published online by Cambridge University Press:  25 June 2019

Emir Yonas Open the ORCID record for Emir Yonas [Opens in a new window] ,
Raymond Pranata Open the ORCID record for Raymond Pranata [Opens in a new window]  and
Nuvi Nusarintowati
Emir Yonas*
Affiliation:
Faculty of Medicine, Universitas YARSI, Jakarta, Republic of Indonesia
Raymond Pranata
Affiliation:
Faculty of Medicine, Universitas Pelita Harapan, Banten, Republic of Indonesia
Nuvi Nusarintowati
Affiliation:
Faculty of Medicine, Universitas Indonesia, Jakarta, Republic of Indonesia
*
Author for correspondence: Emir Yonas, Faculty of Medicine, Universitas YARSI, Jl. Letjend Suprapto No.1, RT.10/RW.5, Cemp. Putih Tim., Cemp. Putih, Kota Jakarta Pusat, Daerah Khusus Ibukota Jakarta 10510, Republic of Indonesia, South East Asia. Tel: +628158759426. E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

We present a case of an 11-year-old Indonesian female who was referred to our facility after surgical excision of brain abscess. The patient has been previously diagnosed with right atrial isomerism, complete atrioventricular septal defect, and L-Transposition of great arteries. Multiple staged surgeries are required for the management of this condition.

Keywords

Heterotaxyisomerismpaediatriccongenital
Type
Brief Report
Information
Cardiology in the Young , Volume 29 , Issue 7 , July 2019 , pp. 999 - 1001
Copyright
© Cambridge University Press 2019 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Jacobs, JP, Anderson, RH, Weinberg, PM, et al. The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy. Cardiol Young 2007; 17 (Suppl 2): 1.Google ScholarPubMed
Sapire, DW, Ho, SY, Anderson, RH, et al. Diagnosis and significance of atrial isomerism. Am J Cardiol 1986; 58: 342.CrossRefGoogle ScholarPubMed
Kawahira, Y, Kishimoto, H, Kawata, H, et al. Morphologic analysis of common atrioventricular valves in patients with right atrial isomerism. Pediatr Cardiol 1997; 18: 107.CrossRefGoogle ScholarPubMed
Uemura, H, Anderson, RH, Ho, SY, et al. Left ventricular structures in atrioventricular septal defect associated with isomerism of atrial appendages compared with similar features with usual atrial arrangement. J Thorac Cardiovasc Surg 1995; 110: 445.CrossRefGoogle ScholarPubMed
Gilljam, T, McCrindle, BW, Smallhorn, JF, et al. Outcomes of left atrial isomerism over a 28-year period at a single institution. J Am Coll Cardiol 2000; 36: 908.CrossRefGoogle Scholar
Hirooka, K, Yagihara, T, Kishimoto, H, et al. Biventricular repair in cardiac isomerism. Report of seventeen cases. J Thorac Cardiovasc Surg 1995; 109: 530.CrossRefGoogle ScholarPubMed
Hill, SJ, Heiss, KF, Mittal, R, et al. Heterotaxy syndrome and malrotation: does isomerism influence risk and decision to treat. J Pediatr Surg 2014; 49: 934.CrossRefGoogle ScholarPubMed