scholarly journals Rapid Progression of Neonatal Respiratory Distress from Laryngeal Cleft Type I: A Case Report

Author(s):  
Doi Yumi ◽  
Nishijima Eiji
PEDIATRICS ◽  
1977 ◽  
Vol 59 (6) ◽  
pp. 1057-1058
Author(s):  
Eduardo Mazzi ◽  
John J. White ◽  
Hiroshi Nishida ◽  
Herman M. Risemberg

Hemothorax that produces acute respiratory distress in a newborn occurs rarely; only ten cases have been reported.1-9 We report another case (associated with hypoprothrombinemia and anemia) in a full-term infant. Thoracentesis successfully relieved the respiratory distress, and transfusion and parenteral vitamin K therapy reversed the bleeding diathesis. CASE REPORT A girl, weighing 3,070 gm, was born to a 30-year-old woman, after spontaneous labor and uncomplicated delivery. The Apgar score was 7 at one and five minutes. The infant was brought to the nursery at 10 minutes of age, where she was found to be a cyanotic black girl with grunting respirations and intercostal retractions.


2015 ◽  
Vol 129 (4) ◽  
pp. 403-405 ◽  
Author(s):  
L Lane ◽  
S Prudon ◽  
T Cheetham ◽  
S Powell

AbstractBackground:A lingual thyroid is a known cause of oropharyngeal obstruction in the neonate. It can be asymptomatic, or present as stridor, dysphonia, dysphagia or dyspnoea with faltering growth. The therapeutic options include surgical resection.Case report:A 6-day-old female neonate, born at 36 weeks gestation, presented with stridulous breathing and poor feeding. Although the cause was initially thought to be laryngomalacia, nasendoscopy revealed a lingual thyroid. The baby had deranged thyroid function, as detected on neonatal screening, but this result was not available until a later date. Despite being symptomatic, the patient was managed medically; thyroxine therapy was associated with resolution of the respiratory symptoms.Conclusion:Nasendoscopy provides valuable information about an ectopic thyroid gland. Thyroid replacement therapy may help to suppress the size of the ectopic gland and ultimately prevent an unnecessary surgical procedure.


2003 ◽  
Vol 22 (3) ◽  
pp. 209-211 ◽  
Author(s):  
Salah Ahmed Ibrahim, FRCP, MD ◽  
Haydar Abubakr Abdalla, FRCS ◽  
Ahmed Mohammed El Hassan, FRCPath, PhD

2018 ◽  
Vol 18 (2) ◽  
pp. 211
Author(s):  
Salma M. Al-Sheibani ◽  
Kiran P. Sawardekar ◽  
Salwa J. Habib ◽  
Hunaina M. Al-Kindi

A salivary gland anlage tumour (SGAT) is a very rare type of benign tumour that usually presents in early infancy with respiratory distress which is exacerbated upon feeding. We report a full-term male neonate who was referred to the Al Nahdha Hospital, Muscat, Oman, in 2015 with severe neonatal respiratory distress due to a nasopharyngeal obstruction immediately after birth. Computed tomography and magnetic resonance imaging revealed a well-circumscribed mass in the nasopharynx, without intracranial extension. Histopathological analysis of the lesion confirmed a diagnosis of SGAT. Following excision of the tumour, the postoperative period was uneventful. No recurrence was observed over the next two years. This case report highlights the importance of the early recognition of this extremely rare and potentially life-threatening, yet easily curable, condition.Keywords: Nasopharyngeal Neoplasms; Salivary Gland Neoplasms; Neonatal Respiratory Distress Syndrome; Case Report; Oman.


2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Penelope Thaller ◽  
Catherine Blanchet ◽  
Maliha Badr ◽  
Renaud Mesnage ◽  
Nicolas Leboucq ◽  
...  

2014 ◽  
Vol 19 (2) ◽  
pp. 109 ◽  
Author(s):  
Vaibhav Pandey ◽  
Preeti Tiwari ◽  
Jayanto Tapadar ◽  
AjayNarayan Gangopadhyay

2014 ◽  
Vol 99 (Suppl 2) ◽  
pp. A497.2-A497
Author(s):  
H Besbès ◽  
H Mhabrech ◽  
A Zrigue ◽  
K Ben Ameur ◽  
K Monastiri ◽  
...  

2003 ◽  
Vol 22 (3) ◽  
pp. 209-211 ◽  
Author(s):  
Salah Ahmed Ibrahim, FRCP, MD ◽  
Haydar Abubakr Abdalla, FRCS ◽  
Ahmed Mohammed El Hassan, FRCPath, PhD

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