Open Medicine (Jan 2016)

Prenatal diagnosis, 3-D virtual rendering and lung sparing surgery by ligasure device in a baby with “CCAM and intralobar pulmonary sequestration”

  • Molinaro Francesco,
  • Angotti Rossella,
  • Garzi Alfredo,
  • Di Crescenzo Vincenzo Giuseppe,
  • Cortese Antonio,
  • Messina Mario

DOI
https://doi.org/10.1515/med-2016-0038
Journal volume & issue
Vol. 11, no. 1
pp. 200 – 203

Abstract

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Congenital cystic lung lesions are a rare but clinically significant group of anomalies, including congenital cystic adenomatoid malformation (CCAM), pulmonary sequestration, congenital lobar emphysema (CLE) and bronchogenic cysts. Despite the knowledge of these lesions increasing in the last years, some aspects are still debated and controversial. The diagnosis is certainly one aspect which underwent many changes in the last 15 years due to the improvement of antenatal scan and the introduction of 3-D reconstruction techniques. As it is known, a prompt diagnosis has an essential role in the management of these children. The new imaging studies as 3D Volume rendering system are the focus of this paper. We describe our preliminary experience in a case of hybrid lung lesion, which we approached by thoracoscopy after a preoperative study with 3D VR reconstruction. Our final balance is absolutely positive.

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