Journal of Pediatric and Neonatal Individualized Medicine (Aug 2017)

Rare lymphatic malformation in an extreme premature infant: question

  • Veronica Mugarab Samedi,
  • Adel Elsharkawy

DOI
https://doi.org/10.7363/060209
Journal volume & issue
Vol. 6, no. 2
pp. e060209 – e060209

Abstract

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Our patient was born to a healthy 35-year-old Asian mother. The pregnancy was uneventful until 25 weeks of gestational age (GA), when she had preterm prolonged rupture of membranes (PPROM). Ultrasound at that point showed a new finding (confirmed by MRI) of 4.7 x 4.1 cm heterogenous cystic skin-covered mass with areas of echogenicity on the posterior aspect of the fetus with blood flow to the mass and minimal vascularity overall. The male infant was delivered at 26 + 4 weeks by emergency caesarian section for fetal distress with birth weight of 720 grams. A significant finding was a massive swelling over the upper back with a firm central mass. Total size of swelling was 10.2 x 12.2 cm, central cystic mass was smaller (5.0 x 4.2 cm), firm in consistency, slightly mobile, non-pulsatile, non-compressible and non-translucent. Examination of mass did not cause changes in vital signs, thus the mass was considered as a painless malformation. • What is your diagnosis? • Which further investigations would you suggest? • Which subspecialties need to be involved in the management of this case?

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