MCQ Esophagus - Achalasia, Scleroderma, Plumner vinson syndrome

  1. Barium swallow features of achalasia cardia?
    • Dilated esophagus with a distal narrowing
    • “Bird’s beak” ,“Pencil-tip” or “Rat’s tail” appearanceQ
    • Note - “Rat-tail” filling defectQ in carcinoma esophagus
  2. Manometry test in achalasia?
    • Manometry is gold standard test for diagnosis of achalasia.
    • Abnormalities in LES - Incomplete or absent LES relaxationQ • Elevated LES pressureQ
    • Abnormalities in esophageal body - Incomplete or absent LES relaxationQ • Elevated LES pressureQ• Elevated intraesophageal pressureQ (pressurization of the esophagus) from incomplete air evacuation • Simultaneous mirrored contractions with no evidence of progressive peristalsisQ• Low-amplitude waveformsQ indicating a lack of muscular tone
  3. Treatment of choice for achalasia?
    Laparoscopic Heller myotomy is now the operation of choiceQ.
  4. Extent of Heller’s myotomy?
    2 cm above GE junction to 1 cm belowQ, over stomach.
  5. Indications of Esophagectomy in achalasia?
    • Megaesophagus, sigmoid esophagus
    • Failure of more than one myotomy, or
    • Undilatable reflux strictureQ
  6. Mecholyl test and CCK test positive in?
    AchalasiaQ
  7. Chief complains of diffuse esophageal spasm?
    Chest pain and dysphagia, that is heightened in emotional stress
  8. Barium swallow findings in Diffuse esophageal spasm?
    • Corkscrew or rosary-bead esophagus, segmental spasm or pseudodiverticulosis appearanceQ
    • Due to presence of tertiary contractionsQ
  9. Manometry in DES?
    • Manometry is gold standard test for diagnosisQ.
    • Classic manometry findings: Simultaneous, multipeaked contractions of high amplitude (>120 mm Hg) or long duration (>2.5 sec).
  10. Diagnosis of nutcracker esophagus?
    Peristaltic esophageal contractions 2 standard deviations above the normalQ values on manometric tracings.
  11. What is Kilian’s triangle? Q
    Between the upper oblique fibers (thyropharyngeus muscle) and lower horizontal fibers (cricopharyngeus muscle) of the inferior constrictor muscleQ
  12. Features of Zenkers diverticulum?
    • • Increased intraluminal pressures (secondary to abnormal esophageal motility)Q pushes mucosa and submucosa through a muscular defect in the wall of the esophagus creating a pulsion diverticulumQ
    • • It is a pseudodiverticulaQ
    • • It arises posteriorly in the midline of the neck, mouth is in midline but sac projects laterallyQ (usually left laterally)
  13. Patholophysiology of Zenker Diverticulum?
    • • Neuromuscular incordinationQ in this region
    • • May be due to different nerve supply of the two parts of inferior constrictor muscleQ
    • −−The thyropharyngeus (oblique fibers) supplied by the pharyngeal plexus
    • −−Cricopharyngeus (horizontal fibers) by recurrent laryngeal nerve
  14. MC Complications of Zenker Diverticulum?
    Pneumonia and lung abscess due to aspirationQ (MC)
  15. Surgical therapy for Zenker Diverticulum?
    Cricopharyngeal myotomy + Diverticulopexy is treatment of choice
  16. What is Dohlman procedureQ?
    Diverticulo-esophagostomy using a linear cutting staple gun - The septum between the esophagus and the diverticula is divided
  17. Why is Midesophageal diverticulum is also called as Traction Diverticula?
    • Inflammation of the lymph nodes exerts traction on the wall of the esophagus leading to the formation of a true diverticulum in the midesophagus.
    • Caused by inflamed mediastinal lymph nodes from tuberculosis, histoplasmosisQ and resultant fibrosing mediastinitis.
  18. Pathophysiology of scleroderma in GI tract?
    Smooth muscle atrophy in lower two third of esophagus →Incompetent LES →GERD →StrictureQ
  19. Manometry finding in scleroderma?
    Normal peristalsis in the proximal striated esophagus, with absent peristalsis in the distal smooth muscle portion
  20. Treatment of scleroderma?
    Esophageal shortening may require a Collis gastroplasty in combination with a partial fundoplicationQ
  21. What is Plummer-vinson Syndrome?
    • • Also known as Paterson-Brown Kelly syndrome
    • • Occurs in middle aged edentulous (without teeth) womenQ.
    • • Premalignant lesionQ (Approximately 10% of patients develop SCC of esophagus, oral cavity or the hypopharynx)
    • • Iron-deficiency anemia is a common finding (known as sideropenic dysphagiaQ
  22. Cause of dysphagia in Plummer-vinson Syndrome?
    • Cervical esophageal webQ (Post-cricoid web)
    • Abnormal pharyngeal and esophageal motility may play a role.
    • Schatzki’s ring - at the lower end of esophagusQ
Author
surgerymaster
ID
334723
Card Set
MCQ Esophagus - Achalasia, Scleroderma, Plumner vinson syndrome
Description
Esophagus
Updated