Congenital Chylothorax and Hydrops Fetalis: A Novel Neonatal Presentation of RASA1 Mutation

PEDIATRICS ◽  
2021 ◽  
pp. e2020011601
Author(s):  
Alessia Gallipoli ◽  
Gillian MacLean ◽  
Jagdeep S. Walia ◽  
Anupam Sehgal
2021 ◽  
Vol 9 ◽  
Author(s):  
Hung-Lin Tai ◽  
Tze Yee Diane Mok ◽  
An-Shine Chao ◽  
Shih-Ming Chu ◽  
Reyin Lien

Background: Idiopathic congenital chylothorax is a rare but serious disease. Advancement in perinatal care and the renovated treatment modalities have brought about significant improvement in patient outcome.Objective: To describe the clinical course of severe forms of idiopathic congenital chylothorax, focusing on the development of recent treatment modalities and their impacts.Design: A retrospective cohort by review of medical records in the NICU of a perinatal referral center in Taiwan. Study period was from January 2006 to June 2017. Neonates with the diagnosis of idiopathic congenital chylothorax with non-immune hydrops fetalis were enrolled. Clinical relevant including demographic data, perinatal interventions, post-natal course, and treatment outcome were described and analyzed.Results: Twenty-eight neonatal patients were included. The median gestational age at birth was 34 (range 27–36) weeks and median birth weight was 2,369 (range 1,430–3,608) g. Prenatal intervention was performed in 39.3% of the patients. Besides, 11 out of the 28 neonates developed tension pneumothorax in the first 24 h and 4 (36.4%) of them died. Sepsis was documented in two patients (7.1%). Overall survival rate was 71.4%. There were five patients enrolled during the last 2 years of the study period. EXIT with intubation was performed in two and octreotide was given to four of these most recent neonates, and all of them survived.Conclusion: Recent advances in the management of these neonates, specifically EXIT with intubation and use of octreotide. Both of them improved patient survival in our cohort, but the evidence of impact has yet to be validated.


2014 ◽  
Vol 13 (2) ◽  
pp. 70-72
Author(s):  
Yalcin Celik ◽  
Baris Akbas ◽  
Esra Mimaroglu ◽  
Hakan Taskinlar ◽  
Ali Ertug Arslankoylu ◽  
...  

2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Hilal Al Mandhari ◽  
Nidaa Al Naamany ◽  
Asad Ur Rahman ◽  
Hussain Al-Kindy ◽  
Tabinda Naz Qureshi ◽  
...  

Abstract Objectives Congenital chylothorax is a rare entity with various etiologies ranging from anatomical to genetic causes. If associated with non-immune hydrops fetalis mortality rates can reach up to 98%. Treatment is challenging and mostly supportive, with no standard guidelines. Case presentation We describe the unique and challenging course of a late preterm infant with non-immune hydrops fetalis (NIHF), and recurrent chylothorax attributed to homozygous mutations in thrombospondin domain1 (THSD1) gene. The infant was also affected with maple syrup urine disease (MSUD), which further complicated the clinical course. Treatment was supportive by means of chest tubes, intubation, mechanical ventilation, and eventually he was tracheostomized and discharged home on home BiPAP ventilation and required prolonged use of octreotide to prevent re-accumulation of chylothorax. Conclusions THSD1 gene has a role in vascular permeability and its mutation in our patient caused congenital chylothorax and NIHF and is also associated with other features such as vascular malformations.


2021 ◽  
Vol 14 (4) ◽  
pp. e240688
Author(s):  
Alvin Jia Hao Ngeow ◽  
Mei Yoke Chan ◽  
Oon Hoe Teoh ◽  
Sarat Kumar Sanamandra ◽  
Daisy Kwai Lin Chan

A Chinese male infant was born at 35 weeks weighing 2935 g to a mother with polyhydramnios and prenatal hydrops fetalis. He developed marked respiratory distress secondary to bilateral congenital chylothorax and required pleural drainage, high frequency oscillation and inhaled nitric oxide therapy. He was extubated to non-invasive ventilation by day 14. There was no bacterial or intrauterine infection, haematologic, chromosomal or cardiac disorder. He was exclusively fed medium-chain triglyceride formula. High-resolution CT showed diffuse interstitial lung disease. He received a dexamethasone course for chronic lung disease to facilitate supplemental oxygen weaning. A multidisciplinary team comprising neonatology, pulmonology, haematology, interventional radiology and thoracic surgery considered congenital pulmonary lymphangiectasia as the most likely diagnosis and advised open lung biopsy, lymphangiography or scintigraphy for diagnostic confirmation should symptoms of chylothorax recur. Fortunately, he was weaned off oxygen at 5 months of life, and tolerated human milk challenge at 6 months of life and grew well.


2003 ◽  
Vol 120A (1) ◽  
pp. 92-96 ◽  
Author(s):  
Carlo Bellini ◽  
Massimo Mazzella ◽  
Cesare Arioni ◽  
Corradino Campisi ◽  
Gioconda Taddei ◽  
...  

2020 ◽  
Vol 08 (02) ◽  
pp. 176-178
Author(s):  
Dr. Mahmoud M. Osman ◽  
Dr. Mohamed Ali Tagin ◽  
Dr. Mohammed Saleh Alissa ◽  
Dr. Suzan Abdel-Hamid ◽  
Dr. Mohamed Salah Shoeib

2018 ◽  
Vol 31 ◽  
pp. 60-63
Author(s):  
Vilmaris Quinones Cardona ◽  
Michelle Clark ◽  
Margaret Gilfillan ◽  
Randy Stevens

2001 ◽  
Vol 18 (4) ◽  
pp. 371-375 ◽  
Author(s):  
M. Tanemura ◽  
N. Nishikawa ◽  
K. Kojima ◽  
Y. Suzuki ◽  
K. Suzumori

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