Diagnosing the Rare: Clinical Experience in Acardia Twin Recognition - A Case Report

Authors

  • Nor Azam K Department of Family Medicine, Kulliyyah of Medicine, International Islamic University Malaysia, Indera Mahkota Campus, Pahang, Malaysia.
  • Siti Dzulaikha Z Department of Family Medicine, Kulliyyah of Medicine, International Islamic University Malaysia, Indera Mahkota Campus, Pahang, Malaysia.
  • Che Yusof MD Klinik Kesihatan Beserah, Kuantan Pahang, Malaysia.

DOI:

https://doi.org/10.70672/gevann29

Keywords:

Acardiac twin, antenatal diagnosis, fetal outcome, monochorionic twin pregnancy, Twin Reversed Arterial Perfusion (TRAP) sequence.

Abstract

Twin Reversed Arterial Perfusion (TRAP) sequence or acardiac twin, is a rare condition in monochorionic twin pregnancies, presenting significant diagnostic and management challenges. Early detection of TRAP is crucial to improve foetal outcomes, particularly for the pump twin. We report the case of a 37-year-old gravida 5, para 3 + 1, who was initially misdiagnosed with a singleton pregnancy based on clinical and ultrasound examinations conducted at both primary and secondary health facilities. A marked discrepancy between the symphysiofundal height and ultrasound parameters later led to reassessment, revealing a twin pregnancy complicated by TRAP sequence. Radiofrequency ablation (RFA) was successfully performed on the acardiac twin at 28 weeks. The pregnancy ended at 30 weeks gestation with preterm birth, in which the pump twin was delivered alive while the acardiac twin was stillborn. This case highlights the importance of vigilant antenatal assessment, timely diagnosis, and intervention to optimise outcomes in TRAP sequence pregnancies.

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Published

01-11-2024

Issue

Section

Case Report

How to Cite

Nor Azam K, Siti Dzulaikha Z, & Che Yusof MD. (2024). Diagnosing the Rare: Clinical Experience in Acardia Twin Recognition - A Case Report. Asian Journal of Medicine & Health Sciences, 7(2), 288-292. https://doi.org/10.70672/gevann29