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TRACHEA
ANATOMY
Extends from C6 T5/6 vertebrae
Nearly cylindrical, slightly flattened posteriorly 16-20 rings or C-shaped bars, incomplete posteriorly
ANATOMY
Supplied mainly by the inferior thyroid arteries
Receives branches from the superior thyroid, bronchial, and internal thoracic arteries Drained by the inferior thyroid vein Innervated by the vagus, sympathetic, and recurrent laryngeal nerves
TRACHEA AND ESOPHAGUS by JERIEL JOHN C. MAJAM, MD, FPSOHNS
CONGENITAL DISORDERS
Tracheal Agenesis or Atresia Rare There is no continuity between the larynx and trachea Fatal
CONGENITAL DISORDERS
Tracheal Webs Thin band of tissue spanning the tracheal lumen without deformity of the underlying cartilage Tx: Dilation, laser transection; resection and anastomosis
CONGENITAL DISORDERS
Tracheal Stenosis Assoc tracheoesophageal fistula, pulmonary hypoplasia, vascular sling, Trisomy 21 Cartilage is smaller and nonflexible, lacks the posterior membranous portion Dx: endoscopic evaluation Tx: resection and reanatomosis, tracheoplasty
TRACHEA AND ESOPHAGUS by JERIEL JOHN C. MAJAM, MD, FPSOHNS
CONGENITAL DISORDERS
Tracheomalacia Weakness of the tracheal wall resulting in marked exaggeration of movement with respiration Symptoms: Expiratory stridor, wheezing Barking cough Hyperextension of neck Reflex apnea
TRACHEA AND ESOPHAGUS by JERIEL JOHN C. MAJAM, MD, FPSOHNS
CONGENITAL DISORDERS Primary Tracheomalacia Esp in premature infants Dx with rigid endoscopy showing widened posterior wall with expiratory collapse Resolves 18-24 months
TRACHEA AND ESOPHAGUS by JERIEL JOHN C. MAJAM, MD, FPSOHNS
CONGENITAL DISORDERS Secondary Tracheomalacia After surgical repair of tracheoesophageal fistula External compression from vascular anomalies
CONGENITAL DISORDERS
1/3000 livebirths Drooling, coughing, cyanosis, abdominal distention, poor feeding
Clinical Considerations
Foreign body aspiration
More likely to enter right bronchus
Tracheoscopy/bronchoscopy
Ventilating Bronchoscope
TRACHEOSTOMY
Tracheostomy
Is an opening surgically created through the neck into the trachea through which air may pass to the lungs, by-passing through the upper airway.
Tracheostomy
Incidence (2002 PGH)
107 referrals 85% adults
Pneumonia and CVD
BACTERIAL TRACHEITIS
Membranous laryngotracheobronchitis Antibiotis directed vs Staph aureus and H. influenza
ESOPHAGUS
From cricoid cartilage (C6) to stomach (T10)
3 constrictions
Cricopharyngeus Arch of the aorta & left main bronchus Gastro-esophageal junction
ESOPHAGUS
ANATOMY
Blood supply
inf. thyroid br. of thyrocervical trunk small br. of thoracic aorta bronchial aa. ascending br. of left gastric a ascending br. of left phrenic a.
Venous drainage
Inf thyroid Azygos, hemiazygos Gastric
TRACHEA AND ESOPHAGUS by JERIEL JOHN C. MAJAM, MD, FPSOHNS
ANATOMY
Layers:
Outer longitudinal muscle Inner circular muscle Submucosa Mucosa
Congenital
Gastroesophageal reflux
50% of infants; pathologic if it persists beyond 18 months of age Vomiting soon after or up to several hours after feeding Dx: prolonged esophageal pH monitoring Tx: positioning, dietary changes
For Practice
Structural: DIVERTICULA
Caused in part by an area of anatomic weakness 3 areas of constriction Killians dehiscence
Between cricothyroid & cricopharyngeus mm
Lateral dehiscence bet. cricopharyngeus & esophageal muscle fibers through recurrent laryngeal n passes
Symptoms Dysphagia (MC) Spontaneous regurgitation of undigested food Aspiration & cough Halitosis
Barium Swallow
AP View
Barium Swallow
Structural: ACHALASIA
Zonal reduction in ganglion cells Esophageal aperistalsis and LES dysfxn Xray: absent primary peristalsis, beak-like tapering at the esophageal hiatus
Intermittent abn esophageal motility Manometry: presence of simultaneous contractions and intermittent N primary peristalsis
Can be diagnosed through manometry
Xray: absence of primary peristalsis in the smooth muscle portion, corkscrew appearance
Structural: PRESBYESOPHAGUS
Abnormal motility associated with aging Decreased primary and increased tertiary contractions Rule out other concomitant illnesses first
Structural: SCLERODERMA
Aperistalsis of the lower 2/3 of the esophagus Marked decrease in lower esophageal sphincter pressure Normal peristalsis in the upper esophagus 60% with symptomatic dysphagia
Structural: SCLERODERMA
Structural: POLYMYOSITIS
Muscle weakness secondary to inflammation and degenerative changes in striated muscle
Peristalsis is diminished and poorly diminished Esophagus may be dilated
Obesity
Structural: STRICTURES
Schatzkis Ring
Others: MALLORY-WEISS SYNDROME Manifest by bleeding from lacerations of the cardia of the stomach as a result of prolonged or forceful vomiting
LEIOMYOMA
Most common benign tumor L side smooth border R sight irregular border
Inflammatory: PLUMMER-VINSON
Iron deficient anemia, upper esophageal web, hypothyroidism, glossitis, gastritis, dysphagia 15% increase incidence of postcricoid SCCA
TRACHEA AND ESOPHAGUS by JERIEL JOHN C. MAJAM, MD, FPSOHNS
ESOPHAGEAL CANCER
4% of cancer deaths Male:female = 5:1 Chronic tobacco & alcohol use Lower 1/3 of esophagus 40-50%
ESOPHAGEAL CANCER
Fungating in appearance Predisposing alcohol and smoking