Unconfigured Ad

Collapse

23/3/2025

Collapse
This topic has been answered.
X
X
 
  • Time
  • Show
Clear All
new posts
  • Admin
    Administrator

    • Sep 2020
    • 6839

    #1

    weekly_question 23/3/2025

    An eleven year old girl presents with difficulty swallowing. An esophagram shows a distended esophagus and “beaking” at the gastroesophageal junction. Upper endoscopy demonstrates dilated esophageal body and puckering at the LES and retained saliva in the esophagus. The treating gastroenterologist performed esophageal pressure topography and noted the integrated relaxation pressure is elevated at 20mmHg and the esophagus has no peristalsis. According to the Chicago Classification of Esophageal Motility, this patient has

    a Type I achalasia

    b Type II achalasia

    c Type III achalasia

    d Diffuse esophageal spasm
    Want to support Pediatric Surgery Club and get Donor status?

    click here!
  • Answer selected by Admin at 03-25-2025, 11:51 AM.
    Admin
    Administrator

    • Sep 2020
    • 6839

    Correct answer
    a Type I achalasia

    Achalasia has been classically defined by conventional manometry as the absence of esophageal peristalsis and incomplete LES relaxation with pressures greater than 10 mm Hg. Using findings from high resolution manometry and esophageal topography, the Chicago Classification redefined esophageal motility disorders. The achalasia subgroup of motility disorders is characterized by elevated median integrated resting pressure (IRP>15 mm Hg). Type I achalasia has no esophageal peristalsis. Type II achalasia patients have panesophageal pressurization >20% of swallows. These patients are more likely to report weight loss. Type III achalasia patients have peristaltic fragmented or spastic contractions. Type III patients frequently report chest pain.

    Diffuse esophageal spasm has normal IRP, normal peristalsis but with >20% of swallows with reduced latency. DES is not in the achalasia family.

    Histologic findings in Type I and Type II achalasia include aganglionosis and neuronal loss. It is thought that Type II achalasia may progress to Type I if untreated. Type III achalasia has no neuronal loss, but has impaired inhibitory postganglionic neuron function.

    Click image for larger version

Name:	repview (1).jpg
Views:	59
Size:	93.4 KB
ID:	14531

    Comment

    • M Abdelbary
      Cool Member
      • Feb 2022
      • 30

      #2
      A

      Comment

      • Reem Mohammed
        True Member
        • Feb 2022
        • 14

        #3
        A

        Comment

        • jorge2309
          True Member
          • Feb 2025
          • 1

          #4
          A

          Comment

          • Abd El wahed
            Cool Member

            • Dec 2020
            • 39

            #5
            A

            Comment

            • Dr.Halah Yasin
              True Member

              • Sep 2024
              • 11

              #6
              A

              Comment

              • Admin
                Administrator

                • Sep 2020
                • 6839

                #7
                Correct answer
                a Type I achalasia

                Achalasia has been classically defined by conventional manometry as the absence of esophageal peristalsis and incomplete LES relaxation with pressures greater than 10 mm Hg. Using findings from high resolution manometry and esophageal topography, the Chicago Classification redefined esophageal motility disorders. The achalasia subgroup of motility disorders is characterized by elevated median integrated resting pressure (IRP>15 mm Hg). Type I achalasia has no esophageal peristalsis. Type II achalasia patients have panesophageal pressurization >20% of swallows. These patients are more likely to report weight loss. Type III achalasia patients have peristaltic fragmented or spastic contractions. Type III patients frequently report chest pain.

                Diffuse esophageal spasm has normal IRP, normal peristalsis but with >20% of swallows with reduced latency. DES is not in the achalasia family.

                Histologic findings in Type I and Type II achalasia include aganglionosis and neuronal loss. It is thought that Type II achalasia may progress to Type I if untreated. Type III achalasia has no neuronal loss, but has impaired inhibitory postganglionic neuron function.

                Click image for larger version

Name:	repview (1).jpg
Views:	59
Size:	93.4 KB
ID:	14531

                Want to support Pediatric Surgery Club and get Donor status?

                click here!

                Comment

                Working...