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CASE REPORT

Endoscopic Treatment of Duodenal evidence of bile. An Olympus GIF-Q180 video gastroscope was
then used to complete the balloon dilation under fluoroscopic
Web in Association With Annular guidance using a CRE PRO Wireguided Balloon Dilatation Cathe-
ter (Boston Scientific, Marlborough, MA) with a balloon length of
Pancreas in an Infant 5.5 cm. Incremental dilatation from 6 to 10 mm (Fig. 3) allowing for
passage of the endoscope to level of D4 and confirming a normal
Jessica Dodkins, Joseph Meredith,
§
distal duodenum containing bile. Duration of inflation was 15 sec-
z
Scott Nightingale, and yzAniruddh V. Deshpande onds at each increment and 10 mm was chosen for the final initial
dilation as this diameter caused a visible tear in membrane and
allowed the endoscope to pass beyond it. A 6Fr nasojejunal feeding

W e report the rare diagnosis of a fenestrated duodenal


membrane with annular pancreas at the same level, and
successful endoscopic management with balloon dilatation. In
tube was placed under vision with negligible bleeding. Postopera-
tively the patient tolerated oral intake in 24 hours and was not reliant
on the nasojejunal tube. Serum lipase was normal. The patient was
presenting this instructive case we outline unique imaging findings discharged on third postoperative day.
of a delayed presentation and approach to management of congeni- Four weeks later, the patient returned for another planned
tal duodenal stenosis. procedure. The follow-up dilation was completed because of con-
cerns over; possibility of restenosis and patient being lost to follow-
CASE REPORT up. The patient did not become symptomatic again in between
An 8-month-old, nonsyndromic girl presented with delayed initial and repeat dilations. A larger diameter was chosen for this
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symptoms of partial upper gastrointestinal (GI) obstruction. These dilation to completely obliterate the membrane. The stenosis was
included persistent and forceful nonbilious vomiting since birth dilated to 13 mm. At 5 weeks post second procedure, barium meal
and history of failure to thrive. The infant had been treated with showed improvement of the stenosis and reduced proximal
acid-suppressive therapy for gastro-oesophageal reflux without duodenal diameter.
improvement. History of polyhydramnios was noted on Six and 12 months postinitial presentation, the patient’s
antenatal screening. weight for age and growth velocity charts improved vastly.
The patient was unwell at presentation with continued non- Failure to thrive was evident throughout the first 6 months of
bilious vomiting, signs of acute dehydration, nil hematemesis and life where weight was persistently below the 5th percentile. At
biochemical changes of hypochloremic alkalosis, consistent with presentation, the patient’s weight for age was on the 25th
gastric outlet obstruction (venous pH 7.5, CO2 43 mmHg, base centile, moving to the 50th centile postprocedure at 22 months
excess 9.2 mmol/L), and hypokalaemia (2.7 mmol/L). Complete of age. The patient is currently on normal diet and remains
blood count, C-reactive protein, serum lipase, and liver function symptom-free.
tests were normal. Abdominal ultrasound performed in the emer-
gency department showed pneumobilia and a subsequent abdominal DISCUSSION
X-ray depicted gastroduodenal pneumatosis (Fig. 1). A nasogastric We believe this is the first report that confirms the safety and
tube was successfully placed, with no reported difficulty or exces- medium-term efficacy of endoscopic balloon dilatation of duodenal
sive trauma, to decompress the bowel. A contrast CT scan of the membrane in conjunction with annular pancreas in an infant.
abdomen was suggestive of duodenal stenosis, an annular pancreas In any infant presenting with persistent vomiting and
without signs of malrotation (Fig. 2). Given the history of non- history of failure to thrive, the differential diagnosis of congeni-
bilious vomiting and nil hematemesis, in conjunction with the tal duodenal obstruction should be considered. It is common for
finding of pneumatosis on imaging before the endoscopy, we duodenal stenosis to present in early infancy, and management
believe that the pneumatosis was because of severe emesis with traditionally involves a surgical by-pass procedure of the
upper gastrointestinal obstruction. obstruction site (1).
After patient stabilization, endoscopy was performed ini- In this rare case of fenestrated duodenal membrane associ-
tially with an Olympus XP-180N (Olympus Medical Systems Corp, ated with an annular pancreas at the same level, it was the cross-
Tokyo, Japan) to visualize the duodenum. The gastric antrum and sectional imaging that allowed for differentiation of the primary
first part of the duodenum were grossly dilated. A membranous cause of the stenosis, prompting endoscopic intervention over
obstruction to the second part of the duodenum proximal to the surgery as has been reported in a handful of cases (1–6).
ampulla was present with a 2–3 mm luminal opening with no Advancing therapeutic endoscopic techniques have the
capacity to reduce the need for surgical intervention and hence
Received July 23, 2017; accepted February 24, 2018.
risk of related complications.
From the Department Paediatric Gastroenterology, the yPaediatric Sur- We chose to offer graded dilatation in 2 sessions, which is
gery, John Hunter Children’s Hospital, the zHealth and Medicine similar to that reported by Poddar et al (3). In that series, as in our
(Priority Research Centre, GrowupWell), and the §Joint Medical Pro- case, there were no recorded complications associated with
gram, University of Newcastle, New South Wales, Australia. the procedure.
Address correspondence and reprint requests to Dr Aniruddh V. Desh- There are case studies utilizing other endoscopic methods of
pande, MCh, PhD, FRACS, Paediatric Urologist and Surgeon, John managing duodenal membranes, including laser membranotomy,
Hunter Children’s Hospital, School of Medicine and Public Health, needle knife, sphincterotome, high-frequency wave-cutting and hot
University of Newcastle, Locked Bag 1, Hunter Region Mail Centre, biopsy forceps that report promising outcomes with minimal com-
NSW 2310, Australia
(e-mail: aniruddh.deshpande1@hnehealth.nsw.gov.au).
plications (1–6). The main possible risks identified include exces-
The authors report no conflicts of interest. sive bleeding, perforation, and damage to the ampulla. One
Copyright # 2018 by European Society for Pediatric Gastroenterology, important case to note is Barabino et al (7) where a 20-month-
Hepatology, and Nutrition and North American Society for Pediatric old girl had complications of profuse bleeding, increased pancreatic
Gastroenterology, Hepatology, and Nutrition enzymes, and scar formation after 3 failed attempts at endoscopic
DOI: 10.1097/MPG.0000000000001977 incision. The patients eventually required a duodenojejunostomy.

JPGN  Volume 67, Number 4, October 2018 e83

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Case Report JPGN  Volume 67, Number 4, October 2018

FIGURE 1. (A) Ultrasound at presentation showing extensive pneumobilia and (B) plain abdominal X-ray showing gastroduodenal pneumatosis
with a dilated stomach and duodenum suggestive a chronic partial upper GI obstruction. GI ¼ gastrointestinal.

FIGURE 2. (A) Intravenous contrast computer tomography depicting a calibre change because of a membrane in the second part of the
duodenum. (B) Depiction of a near-compete obstruction with no contrast able to pass through with an annular pancreas and (C) CT in axial plane
depicting significant wasting of the preampullary duodenum pancreatic tissue noted on either side of the duodenal segment indicative of an
annular pancreas. Site of narrowing consistent with duodenal membrane (thick arrow) depicting annular pancreas (thin arrow). CT ¼computer
tomography.

FIGURE 3. (A and B) Endoscopic views showing cannulation of tiny fenestration in duodenal membrane and subsequent balloon dilatation with
spacious proximal duodenum and (C) a clear waist seen in the balloon at the level of the duodenal membrane whenever inflated under
fluoroscopic vision.

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JPGN  Volume 67, Number 4, October 2018 Case Report

Ziegler et al (8) reported a case of failure of endoscopic laser 2. Blanco-Rodrı́guez G, Penchyna-Grub J, Porras-Hernández J, et al. Trans-
resection, and Torroni et al (6) reported failed attempt at incision luminal endoscopic electrosurgical incision of fenestrated duodenal
using a 5F sphincterotome in a patient with previous surgery for membranes. Pediatr Surg Int 2008;24:711–4.
annular pancreas, because of inability to reach the membrane. 3. Poddar U, Jain V, Yachha S, et al. Congenital duodenal web: successful
In conclusion, in a nonseptic child, gastric pneumatosis and management with endoscopic dilatation. Endosc Int Open 2016;04:
pneumobilia can be indicators of an underlying chronic partial E238–41.
4. Van Rijn R, Van Lienden K, Fortuna T, et al. Membranous duodenal
upper GI obstruction. Endoscopic balloon dilation has the capacity stenosis: initial experience with balloon dilatation in four children. Eur J
to be a safe, minimally invasive approach to the management of Radiol 2006;59:29–32.
congenital membranous duodenal stenosis even in infants. The case 5. Bittencourt P, Malheiros R, Ferreira A, et al. Endoscopic treatment of
we put forth adds to the data already available presenting promising congenital duodenal membrane. Gastrointest Endosc 2017;76:
results worldwide. We acknowledge that there is still some uncer- 1273–5.
tainty surrounding the long-term outcomes of the technique, par- 6. Torroni F, De Angelis P, Caldaro T, et al. Endoscopic membranectomy of
ticularly regarding the associated addition of an annular pancreas. duodenal diaphragm: pediatric experience. Gastrointest Endosc
2006;63:530–1.
7. Barabino A, Arrigo S, Gandullia P, et al. Duodenal web: complications
REFERENCES and failure of endoscopic treatment. Gastrointest Endosc 2012;75:
1. Huang M, Bian H, Liang C, et al. Gastroscopic treatment of membranous 1123–4.
duodenal stenosis in infants and children: report of 6 cases J Pediatr Surg 8. Ziegler K, Schier F, Waldschmidt J. Endoscopic laser resection of a
2015;50:413–6. duodenal membrane. J Pediatr Surgery 1992;27:1582–3.

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