Abstract

Thoracoamniotic shunting is the treatment of choice for management of the fetus with type 1 congenital pulmonary airway malformation. Thoracoamniotic shunting has been performed to reduce life-threatening risks such as fetal hydrops. However, caution is needed because of possible complications. Here, we report that thoracoamniotic shunting can cause histologic changes in the cyst epithelia. In 5 of 8 patients treated prenatally with thoracoamniotic shunting, squamous metaplasia in the cyst epithelia was seen; whereas squamous metaplasia was not found in 6 patients who were not treated with this procedure. Our results reveal that long-term exposure to the intrauterine environment could possibly lead to the change in the nature of cyst epithelium and consequent squamous metaplasia.

Original languageEnglish
Pages (from-to)1413-1417
Number of pages5
JournalHuman Pathology
Volume43
Issue number9
DOIs
StatePublished - Sep 2012

Keywords

  • Congenital pulmonary airway malformation
  • Cyst epithelium
  • Squamous metaplasia
  • Thoracoamniotic shunting

Fingerprint

Dive into the research topics of 'Squamous metaplasia in the cyst epithelium of type 1 congenital pulmonary airway malformation after thoracoamniotic shunt placement'. Together they form a unique fingerprint.

Cite this