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Jejunal atresia with 'apple peel' deformity. A report of eight survivors

C Manning1, A Strauss, M T Gyepes

  • 1Department of Diagnostic Ultrasound, Memorial Hospital Medical Center, Long Beach, California 90801.

Insights

Apple peel atresia, a severe form of jejunal atresia, previously had high neonatal mortality. Modern diagnosis, surgery, and nutrition dramatically improved survival rates, with all eight reported patients surviving.

Area of Science:

  • Pediatric Surgery
  • Neonatalogy
  • Gastroenterology

Background:

  • Apple peel atresia is a severe congenital anomaly of the jejunum.
  • Historically, this condition was associated with high neonatal mortality rates.

Purpose of the Study:

  • To report outcomes of eight patients with apple peel atresia.
  • To discuss the pathophysiology, diagnosis, surgical management, and postoperative care of this condition.

Main Methods:

  • Retrospective case series analysis.
  • Review of diagnostic imaging, surgical procedures, and patient outcomes.
  • Discussion of pathophysiology and management strategies.

Main Results:

  • All eight patients diagnosed with apple peel atresia survived.
  • Significant improvement in survival rates attributed to advancements in care.
  • Successful surgical repair and postoperative management achieved.

Conclusions:

  • Early diagnosis and prompt surgical intervention are critical for survival.
  • Prolonged parenteral nutrition plays a vital role in postoperative recovery.
  • Modern medical and surgical approaches have drastically improved outcomes for apple peel atresia.

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