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Acardiac twin with preserved brain.

B L Petersen1, H Broholm, L Skibsted

  • 1Department of Pathology, University Hospital, Rigshospitalet, Copenhagen, Denmark. rh02875@rh.dk

Fetal Diagnosis and Therapy
|June 16, 2001
PubMed
Summary

Fatal acardiac syndrome, a rare complication of monochorionic twins, involves one twin supplying circulation to both. This case details an acardiac twin with unusual near-normal brain development and external appearance.

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Area of Science:

  • Perinatology
  • Maternal-Fetal Medicine
  • Developmental Biology

Background:

  • Fatal acardiac syndrome is a rare complication of monochorionic twinning, occurring in approximately 1 in 35,000 births.
  • It results from placental arterioarterial and venovenous anastomoses, causing circulatory imbalance between twins.
  • The donor twin sustains circulation for both itself and the recipient acardiac twin, which typically exhibits severe upper body anomalies.

Observation:

  • This report describes a twin pregnancy initially misdiagnosed via ultrasound, where the recipient twin appeared deceased.
  • In the third trimester, this twin presented as an edematous acardiac twin.
  • Notably, this acardiac twin lacked peripheral reduction defects and possessed a nearly normally developed brain.

Findings:

  • A unique case of a recipient acardiac twin with a near-normal external appearance and almost normally developed brain is presented.
  • This acardiac twin was nourished by a surviving twin brother.
  • Such a presentation, particularly the near-normal brain development, has not been previously documented in medical literature.

Implications:

  • This case expands the known spectrum of acardiac twin malformations.
  • It highlights the importance of serial ultrasound monitoring in monochorionic twins.
  • Further research into the developmental pathways and neurological potential of acardiac twins may be warranted.

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