Ultrasound Assessment of the Fetal Pancreas in Normal and Abnormal Pregnancies: A Narrative Review

Hakan Golbasi1

  • 1Department of Perinatologys, Health Sciences University, Izmir City Hospital, Izmir, Turkey.

Insights

Fetal pancreas ultrasound can assess metabolic health and predict risks. Pancreatic size and texture changes in diabetic pregnancies and growth restriction offer insights into fetal adaptation and outcomes.

Area of Science:

  • Obstetrics and Gynecology
  • Fetal Medicine
  • Metabolic Health

Background:

  • Fetal pancreatic development is crucial for glucose-insulin balance and lifelong metabolic health.
  • Obstetric ultrasonography enables in-utero assessment of fetal pancreatic size, morphology, and echotexture.
  • This provides a non-invasive method to study fetal metabolic adaptation in various pregnancy types.

Purpose of the Study:

  • To review human studies on sonographic evaluation of the fetal pancreas.
  • To correlate fetal pancreatic parameters with maternal metabolic status, fetal growth, and perinatal outcomes.
  • To assess the clinical utility of fetal pancreatic ultrasound in high-risk pregnancies.

Main Methods:

  • A narrative review of electronic databases was conducted.
  • Studies reporting sonographic evaluation of the fetal pancreas were identified.
  • A qualitative, theme-based synthesis was performed due to methodological heterogeneity.

Main Results:

  • Fetal pancreatic biometry is reproducible from mid-gestation, correlating with gestational age, abdominal circumference, and estimated fetal weight.
  • In diabetic pregnancies, increased pancreas size and echogenicity correlate with maternal glycemic burden, fetal overgrowth, and adverse outcomes.
  • Pancreatic measurements show potential for early gestational diabetes prediction and identifying low-birthweight risk in growth restriction.

Conclusions:

  • Standardized ultrasound assessment of the fetal pancreas is a feasible and informative adjunct to conventional biometry.
  • It reflects fetal response to diabetic exposure, growth restriction, and syndromic diseases.
  • Further research with harmonized protocols and long-term follow-up is needed for routine clinical integration.

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