scholarly journals Epignathus with Fetiform Features

2011 ◽  
Vol 3 (01) ◽  
pp. 056-058 ◽  
Author(s):  
Kumar Sunil Y. ◽  
Shrikrishna U. ◽  
Jayaprakash Shetty ◽  
Aishwarya Sitaram

ABSTRACTEpignathus is an extremely rare oropharyngeal teratoma that commonly arises from the palate, leading to a high mortality (80-100%) due to airway obstruction in the neonatal period. We present a case of epignathus immature teratoma with fetiform features, originating from basisphenoid in a 28-week preterm male baby, who succumbed to death immediately after birth. Since epignathus is a life-threatening condition at the time of delivery, a prenatal diagnosis is essential to coordinate the treatment and appropriate management by securing the airway, either by endotracheal intubation or tracheostomy followed by complete resection of the tumor.

2015 ◽  
Vol 17 (1) ◽  
pp. 115 ◽  
Author(s):  
Halil Aslan ◽  
Ali Ekiz ◽  
Deniz Kanber Acar ◽  
Burchan Aydiner ◽  
Basak Kaya ◽  
...  

Congenital high airway obstruction syndrome (CHAOS) is an extremely rare life-threatening condition. Laryngeal atresia appears to be the most frequent cause. Generally the diagnosis is made with severely enlarged and highly echogenic lungs and additional ultrasound findings. The prognosis of the affected infants is often poor. Five cases are reported here that were diagnosed in a tertiary center between 2008 and 2014.


2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Piya Chaemsaithong ◽  
Tharintorn Chansoon ◽  
Boonsri Chanrachakul ◽  
Suchin Worawichawong ◽  
Sansanee Wongwaisayawan ◽  
...  

Congenital high airway obstruction syndrome is a rare but life-threatening condition. Therefore, prenatal diagnosis is important. The obstruction can be due to laryngeal/tracheal atresia or external compression. While a differential diagnosis with congenital cystic adenomatoid malformation (CCAM) type III may be difficult, it is still possible with ultrasonography. In this study, we report a case of bilateral echogenic lungs with hydrops fetalis. After the prenatal diagnosis of laryngeal atresia, the couple opted to have an elective termination of pregnancy performed at 20 weeks of gestation. The diagnosis was confirmed by a complete pathological examination.


2018 ◽  
Vol 100 (8) ◽  
pp. e223-e225
Author(s):  
A Matsushita ◽  
S Hosokawa ◽  
D Mochizuki ◽  
J Okamura ◽  
K Funai ◽  
...  

Huge cervical and mediastinal masses may lead to acute respiratory failure caused by laryngotracheal compression and airway obstruction. Thyroid storm is also a life-threatening endocrine emergency originating almost exclusively from uncontrolled Graves’ disease. We report a case of a 42-year-old man with acute upper airway obstruction and tachycardia from progressive swelling of a giant thyroid, in conjunction with thyroid storm resulting from uncontrolled Graves’ disease. Fibreoptic-assisted nasal intubation was performed while the patient was awake, immediately followed by emergency total thyroidectomy via a cervical and sternal approach. The patient had an uneventful postoperative course and recovered well. Respiratory failure due to swelling of a giant thyroid is a life-threatening condition and should be treated immediately with endotracheal intubation while the patient is awake following emergent total thyroidectomy, even with a sternotomy.


2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Razieh Afrough ◽  
Sayyed Shahabeddin Mohseni ◽  
Setareh Sagheb

Chronic Granulomatous Disease (CGD) represents recurrent life-threatening bacterial and fungal infections and granuloma formation with a high mortality rate. CGD’s sign and symptoms usually appear in infancy and children before the age of five; therefore, its presentation in neonatal period with some uncommon features may be easily overlooked. Here we describe a case of CGD in a 24-day-old boy, presenting with a diffuse purulent vesiculopustular rash and multiple osteomyelitis.


2018 ◽  
Vol 2018 ◽  
pp. 1-6
Author(s):  
Boonchai Boonyawat ◽  
Yiwa Suksawat ◽  
Punchama Pacharn ◽  
Piradee Suwanpakdee ◽  
Chanchai Traivaree

Vitamin K deficiency bleeding (VKDB) is a life-threatening condition and can be found in children as early as neonatal period with early onset intracranial hemorrhage (ICH). Here, we reported a 1-year-old boy who initially presented with intracranial hemorrhage secondary to vitamin K deficiency since 3 months of age and later found to have XL-CGD which was complicated by malabsorption due to severe vaccine-associated mycobacterial disease.


PEDIATRICS ◽  
1981 ◽  
Vol 68 (1) ◽  
pp. 103-105
Author(s):  
Jonathan M. Couriel ◽  
Peter D. Phelan

Three patients with severe upper airway obstruction due to subglottic cysts and their subsequent progress and management are described. The relationship of the lesions to intubation in the neonatal period is discussed.


1996 ◽  
Vol 115 (1) ◽  
pp. 138-140 ◽  
Author(s):  
Steven M. Kelly ◽  
Max M. April ◽  
David E. Tunkel

Laryngeal granuloma formation is an unusual complication of endotracheal intubation, especially in young children. Two neonates were evaluated for stridor and life–threatening upper airway obstruction that developed 2 days after birth. Each infant had been endotracheally intubated for several minutes to facilitate meconium suctioning in the delivery suite. Obstructive true vocal cord granulomas were seen at microlaryngoscopy, and surgical excision provided relief of airway obstruction. The pathogenesis and treatment of postintubation laryngeal granulomas are discussed.


2003 ◽  
Vol 112 (7) ◽  
pp. 651-653 ◽  
Author(s):  
Hussein Gadban ◽  
Yoav Talmon ◽  
Peter Gilbey ◽  
Alvin Samet

Acute macroglossia is rare, but may cause upper airway obstruction requiring emergency intervention. The cause of the problem is often obscure. Edema of the tongue may be due to angioedema or to allergy. We present several cases of acute edema of the tongue, in 3 cases causing life-threatening airway obstruction. Among these, we present the first case of acute enlargement of the tongue due to the ingestion of artichoke.


2015 ◽  
Vol 6 (3) ◽  
pp. 118-120
Author(s):  
Billy Wong

ABSTRACT Introduction Endobronchial blood clot causing airway obstruction is a rare but potentially life-threatening condition and can occur in a variety of clinical settings. Case report A male laryngectomy, with a background of bronchogenic carcinoma was treated conservatively for tracheitis following an episode of upper respiratory tract infection. However, he later developed airway obstruction secondary to endobronchial bleeding with endobronchial clot formation. Conventional methods of suctioning and rigid bronchoscopy with forceps failed to remove the hematoma. A Fogarty embolec tomy catheter was used to remove the hematoma, relieving the airway obstruction. Discussion The Fogarty embolectomy catheter has been widely used in various vascular operations for removal of arterial and venous emboli over the last years. However, its application in nonvascular cases is not widely published. Conclusion We report a case of tracheitis, complicated by an endobronchial clot in a laryngectomy patient, and demonstrated the use of Fogarty embolectomy catheter in such case when conventional methods fail. How to cite this article Wong B. The use of a Fogarty Catheter in a Case of an Endobronchial Blood Clot in a Laryn gectomy Patient. Int J Head Neck Surg 2015;6(3):118120.


1981 ◽  
Vol 89 (6) ◽  
pp. 992-997 ◽  
Author(s):  
Lanny Garth Close ◽  
Harvey S. Rosenberg ◽  
Carole Vogler ◽  
Herman E. Warshaw

Two cases of fibromatosis arising in the larynx of neonates are presented, and the literature is reviewed. This tumor represents a rare cause for airway obstruction occurring clinically at birth or early in the neonatal period. Diagnosis and management of this benign but potentially life-threatening lesion are discussed.


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