Achalasia Imaging 

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Achalasia Imaging 

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Achalasia is an esophageal motor disorder characterized by increased lower esophageal sphincter (LES) pressure, diminished to absent peristalsis in the distal portion of the esophagus composed of smooth muscle, and lack of a coordinated LES relaxation in response to swallowing. Patients with achalasia commonly present with dysphagia to solids and liquids, regurgitation unresponsive to proton pump inhibitors, and chest pain. [1, 2, 3, 4, 5, 6, 7]

According to the American College of Gastroenterology,  proper diagnosis of the disorder should include the following [8] :

The Chicago classification is a currently accepted system that separates classic achalasia into 3 clinically relevant subtypes [9, 10] :

The manometric findings common to all types of achalasia include impaired relaxation of the LES (residual pressure or integrated relaxation pressure of ≥10 mmHg) and absent peristalsis in a patient without mechanical obstruction near the LES.

Type I has 100% absent peristalsis and no significant esophageal pressurization.

Type II has 100% absent peristalsis with ≥20% of swallows with pan-esophageal pressurization to >30 mmHg.

Type III has ≥20% of swallows with premature spastic contractions (distal latency of <4.5 s).

Barium swallow studies of achalasia are presented below.

Primary achalasia is the most common subtype and is associated with loss of ganglion cells in the esophageal myenteric plexus. These important inhibitory neurons induce LES relaxation and coordinate proximal-to-distal peristaltic contraction of the esophagus. Secondary achalasia is relatively uncommon. This condition exists when a process other than intrinsic disease of the esophageal myenteric plexus is the etiology. Examples of maladies causing secondary achalasia include certain malignancies, diabetes mellitus, and Chagas disease.

The radiologic examination of choice in the diagnosis of achalasia is a barium swallow study performed under fluoroscopic guidance. [11, 12]  A diagnosis of achalasia supported by the results of radiologic studies must always be confirmed by performing upper gastrointestinal endoscopy and esophageal manometry. These tests allow the direct evaluation and inspection of the esophageal mucosa and an objective measurement of esophageal contractility. [13, 14, 15, 4, 5]

Normal findings on a barium swallow study do not completely exclude achalasia, especially in the condition’s early stages. This situation is when esophageal manometry is most valuable, because the physiologic derangements associated with achalasia precede the development of the anatomic findings discernible by using radiographic studies.

Treatment options for achalasia include pharmacologic, mechanical, botulinum toxin, and surgical-based therapies.

Plain chest radiographs occasionally offer clues in the diagnosis of achalasia. A double mediastinal stripe is occasionally depicted. An air-fluid level can be seen in the esophagus; this is frequently retrocardiac. Owing to the paucity of air progressing through the hypertensive LES, the gastric air bubble may be small or absent. [16]

Radiologic features of achalasia may be difficult to demonstrate, especially early in the disease process. Chest radiographic findings have low sensitivity and specificity for the diagnosis of achalasia. If suspected, achalasia should be confirmed with other radiologic examinations, such as barium swallow study under fluoroscopy, and with upper gastrointestinal endoscopy and manometry. [14, 4, 5]

Features of achalasia depicted at barium study under fluoroscopic guidance include the following (see also the images below):

Failure of peristalsis to clear the esophagus of barium with the patient in the recumbent position

Antegrade and retrograde motion of barium in the esophagus secondary to uncoordinated, nonpropulsive, tertiary contractions

Pooling or stasis of barium in the esophagus when the esophagus has become atonic or noncontractile (which occurs late in the course of disease)

LES relaxation that is incomplete and not coordinated with esophageal contraction

Dilation of the esophageal body, which is typically maximal in the distal esophagus

Tapering of the barium column at the unrelaxed LES, resulting in the bird beak sign

Associated epiphrenic diverticula (possible finding)

According to Schima and coworkers, approximately 90% of patients undergoing barium swallow examination for suspected achalasia have some esophageal dilation and a classic bird beak deformity. [17]

A study from El-Takli and colleagues contradicts this claim. [18] These investigators reviewed the barium-contrast radiographs of 51 patients with manometrically diagnosed achalasia. In only 58% of these studies was achalasia mentioned as a diagnostic possibility by the interpreting radiologist. The radiographs were then provided to an expert gastrointestinal radiologist, mixed in with normal control studies. This expert determined that typical radiologic features of achalasia were absent in 50% of the studies performed on achalasia patients. The authors concluded that barium-contrast radiography is not sensitive for the diagnosis of achalasia, frequently due to the lack of characteristic and detectable radiologic features.

A study by Kostic et al—in which preliminary data were gathered on timed barium esophagograms in patients with achalasia, as well as in normal controls—indicated that further studies are necessary before the clinical usefulness of timed barium esophagograms can be confirmed. [19] Subjects were fasted and then given 250 mL of low-density barium sulfate suspension orally. Radiographs were made 1, 2, and 5 minutes after the start of barium administration. The height and width of the barium column and the rate of change over time were recorded.

The study was repeated in all subjects after an approximate 1-week interval. The controls uniformly achieved complete esophageal emptying within 2 minutes. The height and width of the barium column and the rate of esophageal emptying were all markedly abnormal in the achalasia patients. The static data were very reproducible between studies, but the functional (esophageal emptying) data were not, with a coefficient of correlation of only 0.50.

No normal variants exist; however, several disease processes can mimic achalasia on chest radiographs or barium swallow studies. These include colon adenocarcinoma, esophageal carcinoma, gastric carcinoma, non–small cell lung cancer, thoracic scleroderma, amyloidosis, Chagas disease, collagen-vascular disease, and lymphoma.

According to Gockel and colleagues, pseudoachalasia, caused by carcinomas or other disease processes or by iatrogenic conditions involving the cardia and gastroesophageal junction, may be indistinguishable from achalasia when conventional endoscopic, manometric, and radiologic diagnostic means are used. [20] In their report, the authors found that pseudoachalasia was caused by primary malignancies in 53.9%, secondary malignancies in 14.9%, and benign lesions in 12.6% of the 264 cases in the series. The remainder of the cases (11.9%) were due to sequelae of operations involving the distal esophagus or proximal stomach.

Esophageal motor abnormalities can result from tumor infiltration of the esophageal wall and associated nerve damage. If mucosal irregularity or mass effect is present at the tapered gastroesophageal junction, pseudoachalasia should be considered. The use of amyl nitrite can often be helpful, as the LES relaxes in achalasia but remains fixed in pseudoachalasia.

Computed tomography (CT) scanning with oral contrast enhancement may demonstrate the gross structural esophageal abnormalities associated with achalasia, especially dilatation, which is seen in advanced stages. However, CT findings are nonspecific, and the diagnosis of achalasia cannot be made using CT alone. CT scanning may be indicated in the workup of patients with suspected pseudoachalasia. CT findings should always be confirmed by means of barium swallow study with fluoroscopy, upper gastrointestinal endoscopy, and esophageal manometry.

Disease processes that can mimic achalasia include the following:

Colon adenocarcinoma

Esophageal carcinoma

Gastric carcinoma

Non–small cell lung cancer

Thoracic scleroderma

Amyloidosis

Chagas disease

Collagen-vascular disease

Lymphoma

Ultrasonography is not useful in establishing the primary diagnosis of achalasia. [21] However, Eckhardt et al investigated its utility in the differentiation of true achalasia from pseudoachalasia. [22] The authors performed transabdominal ultrasonography in subjects with achalasia (n = 28), in those with pseudoachalasia (ie, neoplasms of the gastric cardia, n = 13), and in 28 age- and sex-matched controls. They found the sensitivity and specificity rates for ultrasonography in the diagnosis of pseudoachalasia to be 100% and 82%, respectively.

Mittal reported on the utility of high-frequency intraluminal esophageal ultrasonography in various esophageal motor disorders, including achalasia, diffuse esophageal spasm, and nutcracker esophagus. [23] Hypertrophy and asynchrony of the longitudinal and circular muscle layers can be identified. Sustained contraction of the longitudinal muscle layer has been shown to correlate with symptoms such as chest pain and heartburn. This technique is not yet prevalent in clinical practice.

Lacy BE, Weiser K. Esophageal motility disorders: medical therapy. J Clin Gastroenterol. 2008 May-Jun. 42(5):652-8. [Medline].

Patel DA, Kim HP, Zifodya JS, Vaezi MF. Idiopathic (primary) achalasia: a review. Orphanet J Rare Dis. 2015 Jul 22. 10:89. [Medline].

Molena D, Mungo B, Stem M, Lidor AO. Hospitalization for esophageal achalasia in the United States. World J Gastrointest Endosc. 2015 Sep 25. 7 (13):1096-102. [Medline].

Herbella FA, Patti MG. Can high resolution manometry parameters for achalasia be obtained by conventional manometry?. World J Gastrointest Pathophysiol. 2015 Aug 15. 6 (3):58-61. [Medline].

Pandolfino JE, Gawron AJ. Achalasia: a systematic review. JAMA. 2015 May 12. 313 (18):1841-52. [Medline].

Stavropoulos SN, Friedel D, Modayil R, Parkman HP. Diagnosis and management of esophageal achalasia. BMJ. 2016 Sep 13. 354:i2785. [Medline].

Gyawali CP. Achalasia: new perspectives on an old disease. Neurogastroenterol Motil. 2016 Jan. 28 (1):4-11. [Medline].

Vaezi MF, Pandolfino JE, Vela MF. ACG clinical guideline: diagnosis and management of achalasia. Am J Gastroenterol. 2013 Aug. 108 (8):1238-49; quiz 1250. [Medline].

Uppal DS, Wang AY. Update on the endoscopic treatments for achalasia. World J Gastroenterol. 2016 Oct 21. 22 (39):8670-8683. [Medline].

Kahrilas PJ, Bredenoord AJ, Fox M, Gyawali CP, Roman S, Smout AJ, et al. The Chicago Classification of esophageal motility disorders, v3.0. Neurogastroenterol Motil. 2015 Feb. 27 (2):160-74. [Medline].

Chung JJ, Park HJ, Yu JS, Hong YJ, Kim JH, Kim MJ, et al. A comparison of esophagography and esophageal transit scintigraphy in the evaluation of usefulness of endoscopic pneumatic dilatation in achalasia. Acta Radiol. 2008 Jun. 49(5):498-505. [Medline].

Palladino D, Mardighian A, D’Amora M, Roberto L, Lassandro F, Rossi C, et al. Imaging in the Evaluation of Endoscopic or Surgical Treatment for Achalasia. Gastroenterol Res Pract. 2016. 2016:2657876. [Medline].

Gonlachanvit S, Fisher RS, Parkman HP. Diagnostic modalities for achalasia. Gastrointest Endosc Clin N Am. 2001 Apr. 11(2):293-310, vi. [Medline].

Fisichella PM, Raz D, Palazzo F, et al. Clinical, radiological, and manometric profile in 145 patients with untreated achalasia. World J Surg. 2008 Sep. 32(9):1974-9. [Medline].

Rohof WO, Lei A, Boeckxstaens GE. Esophageal stasis on a timed barium esophagogram predicts recurrent symptoms in patients with long-standing achalasia. Am J Gastroenterol. 2013 Jan. 108(1):49-55. [Medline].

Woodfield CA, Levine MS, Rubesin SE, et al. Diagnosis of primary versus secondary achalasia: reassessment of clinical and radiographic criteria. AJR Am J Roentgenol. 2000 Sep. 175(3):727-31. [Medline].

Schima W, Stacher G, Pokieser P, et al. Esophageal motor disorders: videofluoroscopic and manometric evaluation- -prospective study in 88 symptomatic patients. Radiology. 1992 Nov. 185(2):487-91. [Medline].

El-Takli I, O’Brien P, Paterson WG. Clinical diagnosis of achalasia: how reliable is the barium x-ray?. Can J Gastroenterol. 2006 May. 20(5):335-7.

Kostic S, Andersson M, Hellstrom M, et al. Timed barium esophagogram in the assessment of patients with achalasia: reproducibility and observer variation. Dis Esophagus. 2005. 18(2):96-103.

Gockel I, Eckardt VF, Schmitt T, Junginger T. Pseudoachalasia: a case series and analysis of the literature. Scand J Gastroenterol. 2005 Apr. 40(4):378-85.

Sezgin O, Ulker A, Temucin G. Sonographic findings in achalasia. J Clin Ultrasound. 2001 Jan. 29(1):31-40. [Medline].

Eckardt VF, Schmitt T, Kanzler G. Transabdominal ultrasonography in achalasia. Scand J Gastroenterol. 2004 Jul. 39(7):634-7.

Mittal RK. Motor and sensory function of the esophagus: revelations through ultrasound imaging. J Clin Gastroenterol. 2005 Apr. 39(4 Suppl 2):S42-8.

Church JT, Gadepalli SK, Talishinsky T, Teitelbaum DH, Jarboe MD. Ultrasound-guided intrasphincteric botulinum toxin injection relieves obstructive defecation due to Hirschsprung’s disease and internal anal sphincter achalasia. J Pediatr Surg. 2017 Jan. 52 (1):74-78. [Medline].

Moonen A, Boeckxstaens G. Current diagnosis and management of achalasia. J Clin Gastroenterol. 2014 Jul. 48 (6):484-90. [Medline].

Michael AJ Sawyer, MD Consulting Staff, Department of Surgery, Comanche County Memorial Hospital; Medical Director, Lawton Bariatrics

Michael AJ Sawyer, MD is a member of the following medical societies: American Society for Metabolic and Bariatric Surgery, Society for Surgery of the Alimentary Tract, Society of Laparoendoscopic Surgeons, American College of Surgeons, Society of American Gastrointestinal and Endoscopic Surgeons

Disclosure: Nothing to disclose.

Bernard D Coombs, MB, ChB, PhD Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand

Disclosure: Nothing to disclose.

David Andrew Nicholson, MBBS, FRCR Honorary Lecturer, Department of Radiology, University of Manchester Medical School; Consultant Gastrointestinal Radiologist, Department of Radiology, Hope Hospital, Salford Royal Hospital NHS Trust, UK

Disclosure: Nothing to disclose.

Eugene C Lin, MD Attending Radiologist, Teaching Coordinator for Cardiac Imaging, Radiology Residency Program, Virginia Mason Medical Center; Clinical Assistant Professor of Radiology, University of Washington School of Medicine

Eugene C Lin, MD is a member of the following medical societies: American College of Nuclear Medicine, American College of Radiology, Radiological Society of North America, Society of Nuclear Medicine and Molecular Imaging

Disclosure: Nothing to disclose.

Thomas F Murphy, MD Chief of Abdominal Imaging Section, Department of Radiology, Tripler Army Medical Center

Disclosure: Nothing to disclose.

Achalasia Imaging 

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