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Evolution of periventricular leukomalacia during the neonatal period and infancy: correlation of imaging and

L S De Vries1, J S Wigglesworth, R Regev

  • 1Department of Paediatrics and Neonatal Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, London, U.K.

Insights

Cranial ultrasound accurately detects periventricular leukomalacia (PVL) in infants. While ultrasound lesions may resolve, pathological examination reveals lasting effects like glial scarring and impaired myelination.

Area of Science:

  • Neonatal Neurology
  • Pediatric Radiology
  • Neuropathology

Background:

  • Periventricular leukomalacia (PVL) is a significant cause of neurological morbidity in preterm infants.
  • Accurate diagnosis of PVL is crucial for timely intervention and management.
  • Cranial ultrasound is a widely used imaging modality for neonatal brain assessment.

Purpose of the Study:

  • To evaluate the diagnostic accuracy of cranial ultrasound for periventricular leukomalacia (PVL).
  • To correlate ultrasound findings with postmortem neuropathology to establish the natural history of PVL.
  • To assess the long-term sequelae of PVL despite apparent resolution on ultrasound.

Main Methods:

  • Retrospective analysis of cranial ultrasound studies in 68 infants over 4 years, with subsequent necropsy.
  • Correlation of in-life ultrasound diagnoses with postmortem findings in 18 infants with PVL.
  • Sequential ultrasound studies in 11 infants were compared with postmortem data to track PVL evolution.

Main Results:

  • Cranial ultrasound demonstrated 91% accuracy, 72% sensitivity, and 98% specificity for PVL diagnosis.
  • Early PVL showed small hemorrhages on postmortem in infants dying within 7 days.
  • Cystic lesions were observed in life and postmortem, with resolution on ultrasound in long-term survivors, but pathological changes persisted.

Conclusions:

  • Cranial ultrasound is a reliable tool for diagnosing PVL in infants.
  • Ultrasound-detected PVL lesions can resolve over time, but underlying neuropathological changes like glial scarring and impaired myelination persist.
  • Understanding the natural history of PVL is essential for interpreting imaging findings and predicting long-term outcomes.

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