Congenital chylothorax in an extreme preterm newborn

Authors

  • Lil Katia Rodríguez-Díaz Universidad de Ciencias Médicas. Hospital Universitario Gineco-Obstétrico Mariana Grajales. Servicio de Neonatología. Villa Clara, Cuba. https://orcid.org/0000-0002-1186-589X
  • Ana Miriam Clemades-Méndez Universidad de Ciencias Médicas. Hospital Universitario Gineco-Obstétrico Mariana Grajales. Servicio de Neonatología. Villa Clara, Cuba. https://orcid.org/0000-0001-6548-6361
  • Seydis Chaviano-Rodríguez Universidad de Ciencias Médicas. Hospital Universitario Gineco-Obstétrico Mariana Grajales. Servicio de Neonatología. Villa Clara, Cuba. https://orcid.org/0000-0003-3929-5355
  • Eduardo Augusto Kedisobua-Clemades Estudiante 4to año de Medicina. Universidad de Ciencias Médicas. Facultad de Medicina. Villa Clara, Cuba. https://orcid.org/0000-0002-0557-8050

Abstract

Introduction: Congenital chylothorax is a rare respiratory disease; however, it is the most common cause of pleural effusion in live newborns.
Objective:
To present a case of congenital chylothorax as an uncommon cause of respiratory distress in a newborn treated at the Gyneco-Obstetric Hospital of Villa Clara.
Case report:
Male patient, who was born at 26.2 weeks of gestational age, by eutocic delivery, with membrane time rupture of an hour, meconium amniotic fluid, to whom was given an Apgar score of 7/8 (normal) and a birth weight of 950 grams; with diagnose of connatal sepsis was necessary to treat with mechanical ventilation. At six days of age presented a clinical deterioration, with decrease of the vesicular murmur in the right hemithorax and at chest X-ray was observed a veiled right lung. The chest ultrasound confirmed a right pleural effusion that was punctured and the study of the drained fluid showed characteristics of a chylothorax. Conservative treatment was indicated (with complete parenteral feeding: traximin without lipid intake) and subsequently with milk rich in short and medium chain fatty acids (Enfaport® from Nestlé Company). Breastmilk was incorporated 15 days after the diagnose. He required prolonged mechanical ventilation. With a satisfactory evolution, he was discharged from the hospital center.
Conclusions:
The resolution of this entity is achieved through conservative treatment, without the presence of recurrence.

DeCS: CHYLOTHORAX/genetics; INFANT, PREMATURE; PLEURAL EFFUSION; RESPIRATORY DISTRESS SYNDROME, NEWBORN; RESPIRATION, ARTIFICIAL.

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References

1. Antón JL, Luna MC, Gimeno A. Derrame pleural no paraneumónico, quilotórax, hemotórax y mediastinitis. Protoc diagn ter pediatr [Internet]. 2017 [citado 01 Mar 2022];1:211-219. Disponible en: https://www.aeped.es/sites/default/files/documentos/13_derrame_pleural.pdf

2. Lima AL, Tresoldi M, Ramos CD, de Melo Alexandre A, Mendes R, Appenzeller S, et al. Quilotórax bilateral espontâneo apôs vômitos excessivos em criança. Rev Paul Pediatr [Internet]. 2016 [citado 04 Feb 2019];34(2):518-21. Disponible en: https://www.academia.edu/58800410/Quilotórax_bilateral_espontâneo_após_vômitos_excessivos_em_criança

3. Fuentes MJ, Novoa J, Contreras I, Vega Briceño L. Quilotórax congénito: una causa rara de distres neonatal. Reporte de caso. Neumo pediátr [Internet]. 2010 [citado 25 Feb 2019];5(2):104-8. Disponible en: https://www.neumologia-pediatrica.cl/PDF/201052/quilotorax.pdf

4. Roehr CC, Jung A, Proquitté H, Blankenstein O, Hammer H, Lakhoo K, et al. Somatostatin or octreotide as treatment options for chylothorax in young children: a systematic review. Intensive Care Med [Internet]. 2006 [citado 01 Mar 2022];32(5):650-7. Disponible en: https://link.springer.com/article/10.1007/s00134-006-0114-9

5. Salgado Andino CA. Tratamiento conservador del quilotórax posquirúrgico en paciente pediátrico. Cambios [Internet]. 2021 [citado 01 Mar 2022];20(1):94-8. Disponible en: https://revistahcam.iess.gob.ec/index.php/cambios/article/view/524/447

6. Büttiker V, Fanconi S, Burger R. Chylothorax in children. Guidelines for diagnosis and management. Anionic Chest [Internet]. 1999 [citado 29 Ene 2022];116(3):682-7. Disponible en: https://doi.org/10.1378/chest.116.3.682

7. Church J, Antunez A, Dean A, Deatrick K, Attar M, Gadepalli S. Evidence-based management of chylothorax in infants. J Pediatr Surg [Internet]. 2017 [citado 27 Feb 2022];52(6):907-12. Disponible en: https://doi.org/10.1016/j.jpedsurg.2017.03.010

8. Christofe N, Ximenes C. Incidence and Treatment of Chylothorax in Children Undergoing Corrective Surgery for Congenital Heart Diseases. Braz J Cardiovasc Surg [Internet]. 2017 [citado 28 Ene 2022];32(5):390-3. Disponible en: https://www.doi.org/10.21470/1678-9741-2017-0011.

9. Meizoso AI, Cervantes M, Rodríguez LA. Quilotórax neonatal. MediCiego [Internet]. 2017 [citado 01 Mar 2022];23(4):[aprox. 5 p.] Disponible en: https://www.revmediciego.sld.cu/index.php/mediciego/article/view/826/1169

10. Aguilar López LA, Rodríguez Moncada LL, Díaz Díaz AM, Peinado Acevedo JS. Recién nacido prtérmino con quilotórax congénito bilateral, una entidad infrecuente que amenaza la vida. MÉD UIS [Internet]. 2017 [citado 01 Mar 2022];30(1):87-92. Disponible en: https://revistas.uis.edu.co/index.php/revistamedicasuis/article/view/6311/6539

11. Huamán Rodríguez MR, Malca Suarez RM, Peralta Chávez V, Aguilar Urbina EW. Quilotórax congénito en prematuro tardío: reporte de caso. Rev méd Trujillo [Internet]. 2019 [citado 31 Ene 2022];14(2):209-13. Disponible en: http://dx.doi.org/10.17268/rmt.2019.v14i04.08

Published

2022-12-23

How to Cite

1.
Rodríguez-Díaz LK, Clemades-Méndez AM, Chaviano-Rodríguez S, Kedisobua-Clemades EA. Congenital chylothorax in an extreme preterm newborn. Arch méd Camagüey [Internet]. 2022 Dec. 23 [cited 2025 Aug. 3];27:e9792. Available from: https://revistaamc.sld.cu/index.php/amc/article/view/9170

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Section

Case Reports