SURGICAL CONSIDERATIONS
Description: Esophageal diverticula are divided into three anatomic types:
pharyngoesophageal (Zenker’s), midesophageal, and
epiphrenic. Structurally, they are either “true” diverticula—meaning they consist of all three layers of the esophageal wall (mucosa, submucosa, and muscularis)—or “false” diverticula consisting of only mucosa (or mucosa and submucosa). Pharyngoesophageal diverticula account for 60-65% of all cases. These are false diverticula that originate in Killian’s triangle, a weak point in the posterior esophagus, just proximal to the transverse fibers of the cricopharyngeal muscle (
Fig. 7.1-2A). They are associated with incomplete, or discoordinate, upper esophageal sphincter relaxation and the resultant increased hypopharyngeal pressure produces a
narrow-mouthed posterior diverticulum. These diverticula frequently present in the seventh decade and are 2-3 times more common in men. Symptoms depend on the stage of the disease. Early on, patients may complain of vague pharyngeal sensations, dysphagia, cough, and excess salivation. Later, more severe symptoms—such as severe (or frequent) dysphagia, regurgitation of food, halitosis, voice changes, aspiration, and odynophagia (painful swallowing)—may occur.
Surgery is the only effective therapy for Zenker’s diverticulum. Respiratory complications (aspiration) or nutritional deficiencies (weight loss) may be directly attributable to the diverticulum and should not be contraindications to surgery. Multiple different operative approaches are advocated:
diverticulectomy alone, cricopharyngeal myotomy, diverticulectomy with myotomy, and myotomy with suspension of the diverticulum. Myotomy alone, which corrects the underlying physiologic abnormality, is up to 78% effective and may be considered for patients with small (< 2 cm) diverticula.
Diverticulectomy or
suspension should be added if the diverticulum itself is large or dependent. Both procedures are performed via a left cervical incision (
Fig. 7.1-3: inset) and are associated with a low rate of recurrence and complications. The upper esophagus is exposed by retracting the sternocleidomastoid muscle and carotid sheath laterally and the thyroid gland medially. The diverticulum is located in the prevertebral space. Care is taken not to injure the recurrent laryngeal nerve. Following excision of the diverticulum, a cricopharyngeal myotomy may be performed, starting on the upper esophagus and extending across the cricopharyngeal muscle near the neck of the diverticulum, and on to the inferior pharyngeal constrictor muscle.
Recent emphasis has been placed on endoscopic treatment of Zenker’s diverticulum (Dohlman procedure). In this procedure, a modified laryngoscope and endoscopic stapler are used to divide the common wall between diverticulum and true esophageal lumen. This is advantageous because it does not require an incision, and it does not injure the recurrent laryngeal nerve. It has similar results to open procedures.
Midesophageal diverticula, by definition, occur in the middle 3rd of the esophagus. These “true” diverticula typically arise in the setting of mediastinal granulomatous disease whereby a fibrotic reaction around inflamed mediastinal lymph nodes results in traction on the muscular wall of the esophagus. Diverticula usually arise within 4-5 cm of the carina and comprise an estimated 10-17% of all esophageal diverticula. Most midesophageal diverticula are asymptomatic and do not require surgical intervention. In cases that require intervention because of either regurgitation or development of an esophagobronchial fistula, the approach is through a right thoracotomy with excision of the inflammatory mass. Primary closure of the fistula and the interposition of viable tissue, such as muscle, should be performed.
Epiphrenic diverticula arise in the distal 10 cm of the esophagus and are thought to be related to an underlying esophageal motility disorder. These false diverticula are most commonly present in the 6th decade. The clinical presentation is variable; most patients have symptoms related to their underlying dysmotility syndrome: dysphagia, chest pain, or regurgitation. Most patients with epiphrenic diverticula are asymptomatic, and there appears to be no relation between size of the diverticulum and symptoms. Surgery for epiphrenic diverticula typically consists of
diverticulectomy with myotomy either through a
left thoracotomy (
Fig. 7.1-4) or via
laparoscopy. With the transthoracic approach, a low,
left thoracotomy is used, the esophagus is mobilized and encircled, and the diverticulum is mobilized and excised. A
myotomy should be performed opposite the diverticulectomy and should extend proximally above the diverticulum and distally onto the stomach. Because there is, by definition, an underlying motility disorder, the myotomy should be carried onto the stomach, and a nonobstructing
fundoplication may be added to prevent significant postoperative reflux.
Variant procedure or approaches: Laparoscopic diverticulectomy and myotomy has gained increasing acceptance, and reported outcomes are similar to those obtained with the open procedure. The surgical approach is similar to that used during laparoscopic fundoplication (see
p. 585). Dissection of the diverticula may be facilitated by the passage of a bougie or video endoscope. After the diverticulum is amputated using an endoscopic stapler, a myotomy is performed opposite the diverticula, and a partial fundoplication is fashioned.
Usual preop diagnosis: Esophageal diverticulum
Suggested Readings
1. Bock JM, Van Daele DJ, Gupta N, et al: Management of Zenker’s diverticulum in the endoscopic age: current practice patterns. Ann Otol Rhinol Laryngol 2001; 120:796.
2. Dzeletovic I, Ekborn DC, Baron TH: Flexible endoscopic and surgical management of Zenkar’s diverticulum. Expert Rev Gastroenterol Hepatol 2012; 6(4):449-65.
3. Ferreira LE, Simmons DT, Bain TH: Zenker’s diverticula: pathophysiology, clinical presentation, and flexible endoscopic management. Dis Esophagus 2008; 21:1-8.