A5014533294- Tracheal and airway disorders
- Airway Management and Intubation Techniques
- Foreign Body Medical Cases
- Congenital Ear and Nasal Anomalies
- Head and Neck Anomalies
- Voice and Speech Disorders
- Tumors and Oncological Cases
- Teratomas and Epidermoid Cysts
- Dysphagia Assessment and Management
- Restraint-Related Deaths
- Esophageal and GI Pathology
- Oral and Craniofacial Lesions
- Head and Neck Surgical Oncology
- Congenital Diaphragmatic Hernia Studies
- Otitis Media and Relapsing Polychondritis
- Neuroblastoma Research and Treatments
- Cancer and Skin Lesions
- Pectus Deformity Diagnosis and Treatment
- Congenital Heart Disease Studies
- Injury Epidemiology and Prevention
- Vascular Malformations and Hemangiomas
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Lung Cancer Diagnosis and Treatment
- Ocular Disorders and Treatments
- Obstructive Sleep Apnea Research
Hospital Pedro de Elizalde
2016-2024
Garrahan Hospital
2011-2022
Hospital Italiano de Buenos Aires
2013-2015
Infant
2013
Università Cattolica del Sacro Cuore
2011
Objectives/Hypothesis The purpose of this study is to develop consensus on key points that would support the use systemic bevacizumab for treatment recurrent respiratory papillomatosis (RRP), and provide preliminary guidance surrounding modality. Study Design Delphi method‐based survey series. Methods A multidisciplinary, multi‐institutional panel physicians with experience using RRP was established. method used identify obtain characteristics associated across five domains: 1) patient...
Congenital tracheoesophageal fistula not associated with esophageal atresia, known as H-type fistula, is an uncommon anomaly. It presents cough, choking, and cyanosis during feeding and/or recurrent pneumonia. Although symptoms are usually present from birth, diagnosis difficult. The rarity of this disease, non-specific symptoms, the limitations radiological endoscopic confirmation often result in a delay between presentation confirmation. Here we describe clinical manifestations, assessment...
Stridor is a symptom of upper airway obstruction and may result from congenital or acquired causes. The diagnosis usually clinical. If further investigation necessary for differential diagnosis, endoscopy the method choice in most cases. Imaging studies are complementary to endoscopy. They allow evaluation laryngeal tracheobronchial pathology extrinsic compressions due tumors vascular malformations define lesion's location, extent, characteristics. helpful cases diagnostic doubt when...
Subglottic stenosis is a congenital or acquired disease characterized by the narrowing of airways, from vocal cords to lower border cricoid cartilage.It one main causes stridor and respiratory distress in children.More than 90 % laryngeal stenoses are due prolonged endotracheal intubation.The pediatric management subglottic complex may be affected different factors that have an impact on final outcome.Treatment involve endoscopic procedures and/or open surgeries.Here we describe our...
Pediatría práctica RESUMENLa anquiloglosia es una anomalía congénita que se caracteriza por un frenillo lingual anormalmente corto, resulta en grados variables de dificultad la movilidad lingual.Puede ser asintomática o manifestarse con dificultades lactancia, trastornos el habla y dentición, problemas sociales relacionados limitación funcional lengua.Si bien patología frecuente conocida, persisten controversias diversidad opiniones relacionadas indicación, momento método corrección...
Recurrent respiratory papillomatosis is an infrequent benign neoplasm that commonly affects the upper airway with a predilection for larynx. Isolated tracheobronchial involvement very rare. Diagnosis and treatment of this disease challenge due to its non-specific clinical manifestation recurrent nature. We present 6-year-old male diagnosis asthma refractory treatment, without history or evidence laryngeal papillomatosis. The endoscopic examination revealed extensive computed tomography,...
Nasal obstruction in neonates is a potential fatal condition because of their exclusive nasal breathing. The most common congenital causes include choanal atresia, dermoid cyst, glioma and encephalocele. Choanal atresia the anomaly. When bilateral, it presents with respiratory distress at birth. Unilateral manifested by failure unilateral rhinorrhea, may go along unnoticed. Diagnosis suspected absence airfow cavity for inability to advance nasogastric tube. confirmed endoscopic examination...