10 Cr Killian Jamieson Diverticulum

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    Journal of The Association of Physicians of IndiaVol. 63November 2015 65

    Killian-Jamieson Diverticulum:Cervical Oesophageal Diverticulum

    Vinay G Zanwar1, Pravir A Gambhire1, Ajay S Choksey2, Pravin M Rathi3

    Abstract

    Killian-Jamieson (K-J) diverticulum is an outpouching from the lateral wall ofthe proximal cervical oesophagus and isless commonly encountered comparedto Zenkers diverticulum (ZD). These diverticulae arise between the fibers of thecricopharyngeus muscle superiorly and longitudinal muscle of the oesophagusinferiorly. In this report we present a case of a symptomatic Killian Jamiesondiverticulum and review the clinical presentation, differential diagnosis andradiological findings that distinguish it from the more common Zenkersdiverticulum.

    1Resident, 2Lecturer, 3Prof. and Head, Department of Gastroenterology, TNMC and B.Y.L. Nair Hospital, Mumbai, Maharashtra

    Received: 05.08.2014; Revised: 11.12.2014; Accepted: 18.12.2014

    Introduction

    K illian Jamieson (K-J) is a cervicaloesophageal diverticulum, whichis encountered rarely as compared

    to Zenkers diverticulum (ZD), with

    an incidence rat io of 1 :4 . 1 These

    diverticulae arise between the fibers

    o f t h e c r i c o p h a r y n g e u s m u s c l e

    superiorly and longitudinal muscle

    of the esophagus inferiorly.2 This gap

    was first described by Killian3 and it

    represents the area where the recurrent

    laryngeal nerve enters the pharynx

    (Figure 1). This finding was later

    confirmed by Jamieson4 and is now

    termed as Killian-Jamieson triangle.5

    Case Report

    A t w e n t y t w o y e a r o l d l a d y

    presented with progressive dysphagia

    to solids and liquids which developed

    over four months; she also experienced

    night time coughing and hoarsenessaccompanied by reflux symptoms.

    She denied having odynophagia ,

    halitosis, weight loss or anorexia. She

    enjoyed good health till the onset of

    these symptoms for which she was

    prescribed pantoprazole 40 mg twice

    a day and domperidone 10 mg three

    times a day and was doing well with

    above medications. An examination of

    the head and neck was unremarkable.

    Contrast oesophagogram revealed a

    large sac at the level of D1 vertebra with

    no cricopharyngeal bar. Axial CT neck

    and thorax (Figure 2) demonstrated

    31.3 cm outpouching of right lateral

    oesophageal wall at level of C7-D1

    vertebra having a broad neck (24 6

    mm) with evidence of pooling of orally

    administered contrast. There was no

    evidence of perilesional fat stranding.

    Oesophagogastroscopy revealed a large

    pharyngoesophageal diverticulum

    at 16 cm from incisors (Figure 3).

    Oesophageal motility disorders were

    ruled out by oesophagogram. Her

    symptoms got relieved and hence

    patient was not willing to undergo

    surgical treatment.

    Discussion

    A K - J d i v e r t i c u l u m i s o f t e n

    un reco gn iz ed a n d mis d ia gn o s ed

    a s a Z e n k e r s d i v e r t i c u l u m o n

    endoscopy. It has also been referred

    to as a proximal lateral cervicaloesophageal diverticulum or as a

    l a t e r a l d i v e r t i c u l u m f r o m t h e

    pharyngoesophageal junction area.2 It

    is not a true diverticulum as it does not

    involve all layers of the gastrointestinal

    wall.6 Its pathogenesis is unclear.

    D y s c o o r d i n a t i o n o f p h a r y n g e a l

    constrictors, cricopharyngeal spasm,

    fa i lure of relaxat ion of sphincter

    and premature contract ions have

    been implicated. But manometr ic

    and radiographic studies have failed

    to unleash underlying mechanism

    of such pulsion-type diverticulum.

    Cervical oesophageal diverticulae

    C A S E R E P O R T S

    Fig. 1: Anatomic location of Zenkers and Killian-Jamieson diverticulum

    Inferior Constrictor Muscle

    Zenkers Diverticulum

    Cricopharyngeus Muscle

    Esophagus

    Kilian JamiesonDiverticulum

    Recurrent LaryngealNerve

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    Journal of The Association of Physicians of IndiaVol. 63November 201566

    Fig. 2: CT (neck and thorax)demonstrated (bold red arrow)

    outpouching of right lateralesophageal wall with pooling oforally administered contrast

    Fig. 3: Diverticulum (bold blue

    arrow) seen duringoesophagogastroscopy onlateral wall of true lumen

    (vertical black arrow)

    typically present with oropharyngealdysphagia. Retention of food material

    and secretions in the diverticulum

    can result in regurgitation, halitosis,

    chronic cough, and even aspiration

    pneumonia in large diverticulum. These

    symptoms are more likely with ZD.

    However overflow aspiration do not

    occur in patients with Killian-Jamieson

    diverticulae as oesophagography has

    shown cricopharyngeus muscle closure

    in all patients with Killian-Jamieson

    diverticulae.7

    Dysphagia, cough and epigastric

    pain are the most common symptomsexperienced by patients with Killian-

    Jamieson diverticulum. In 2001, Rubesin

    and Levine reviewed the records and

    pharyngoesophagogram of sixteen

    patients with K-J Diverticulum and

    found eleven with symptoms.1Accurate

    differentiation of K-J and Zenkers

    diverticulum requires radiographic

    studies. On barium oesophagogram,

    Zenkers d ivert iculum is seen on

    latera l v iew, 7 often with contrast

    retained within the diverticulum.

    A prominent cricopharyngeal bar is

    often observed. A Killian-Jamieson

    diverticulum is seen on the lateral wall

    of the pharyngoesophageal junction

    on anteroposterior view and with

    contrast possibly being retained. 2, 7

    At times this differentiation becomes

    difficult in large diverticulum with

    extension below. More precise type and

    location of diverticulum can only be

    obtained with the axial CT scan of neck.

    Additional advantage being detection

    of an occult malignancy arising in the

    wall of long standing diverticulum, the

    reported incidence of same being 0.4%. 8

    Only symptomatic patients or those

    having large diverticulae should be

    treated. Due to the rare presentation

    of Killian-Jamieson diverticulae, its

    suggested management is scarce inliterature.2,8,9 The treatment options

    are ei ther surgica l or endoscopic

    diverticulotomy or diverticulectomy

    w i t h o e s o p h a g o m y o t o m y . 6 , 9

    Diverticulectomy has been the preferred

    approach in patients who are good

    surgical candidates. The only major

    concern in this is the risk of causing

    mediastinitis. The diverticulotomy

    creates a communication between the

    diverticular sac and the esophageal

    lumen for free drainage of food material

    without retention inside. Additional

    o es o ph a go myo t o my re l iev es t h epotential functional obstruction in the

    circular oesophageal muscle inferior to

    the diverticula. Endoscopic treatment

    of lateral diverticulae poses inherent

    risk of recurrent laryngeal nerve injury

    because of their intimate relationship

    in t h e K- J t r ia n gle . H o w ev er in

    recent times, the surgical approach

    is being challenged by endoscopic

    diverticulotomy. 6,9 It has been proved

    to be safe and successful. The method

    involves the use of a needle-knife, an

    isolated-tip needle-knife papillotome

    (Iso-Tome) for the dissection of the

    tissue bridge of the diverticulum and

    the use of fitted overtube, a nasogastric

    tube, diverticulosope for adequate

    visualization of the tissue bridge and

    protection of the surrounding tissue.10

    Diverticulopexy can be considered

    alternative to diverticulectomy.6

    However definitive recommendation

    cannot be made and the approach hasto be individualized according to local

    expertise and patient preference.

    References

    1. Rubesin SE, Levine MS. Killian-Jamieson diverticula:

    Radiographic findings in 16 patients. Am J Roentgenol

    2001; 177:859.

    2. Ekberg O, Nylander G. Lateral diverticula from the

    pharyngoesophageal junction area. Radiology1983;

    146:11722.

    3. Killian G. ber den Mund der Speiserhre. Zeitschrift fr

    Ohrenheilkunde 1908; 55:1-44.

    4. Jamieson EB. In: Illustrations of regional anatomy.

    Edinburgh: EandS Livingstone Ltd, 1934; (Section 2):44

    5. Zaino C, Jacobson HG, Lepow H, Ozturk C. Thepharyngoesophageal sphincter. Springfield: CC Thomas,

    1950; 29-144.

    6. CH Chea, SL Siow, TW Khor, NA Nik Azim. Killian-

    Jamieson Diverticulum: The Rarer Cervical Esophageal

    Diverticulum. Med J Malaysia2011; 66:73-4.

    7. Eckberg O. Radiology of the Pharynx and the Esophagus.

    Berlin: Springer-Verlag, 2003.

    8. Rogers PJ, Armstrong WB, Dana E. Killian-Jamieson

    diverticulum: A case report and a review of the literature.

    Ann Otol Rhinol Laryngol2000; 109:1087-97.

    9. Tang SJ, Tang L, Chen E, Myers LL. Flexible endoscopic

    Killian-Jamieson Diverticulotomy and literature review

    (with video). Gastrointest Endosc2008; 68:7903.

    10. Chang Kyun Lee. Endoscopic diverticulotomy with an

    isolated-tip needle-knife papillotome (Iso-Tome) and a

    fitted overtube for the treatment of a Killian-Jamieson

    diverticulum. World J Gastroenterol 2008; 14:6589-92.