A 59-year-old man with hilar cholangiocarcinoma and subsequent
thrombosis of the intrahepatic portal vein presented with acute upper
gastrointestinal hemorrhage. Esophagogastroduodenoscopy revealed acute bleeding
from distal esophageal grade III varices ([Fig. 1 a]).
Fig. 1 a Bleeding
esophageal varix located directly above the esophagogastric junction.
b Self-expanding metal stent in the esophagus
immediately after implantation.
Variceal band ligation was unsuccessful, and the patient rapidly
developed respiratory failure because of aspiration of regurgitated blood.
After intubation and artificial ventilation, placement of a nitinol
self-expanding metal stent (SX-Ella Danis, Hradec Králové, Czech
Republic) immediately stopped the hemorrhage, as also confirmed endoscopically
1 day later ([Fig. 1 b]).
The post-procedure clinical course was uneventful; artificial
ventilation was continued because of aspiration pneumonia. However, after 6
days, respiratory parameters deteriorated rapidly due to severe bronchial
obstruction. Endotracheal bronchoscopy revealed profound narrowing of the
proximal left main bronchus near the main carina because of extraluminal
compression ([Fig. 2 a]).
Fig. 2 Bronchoscopic view of
left main bronchus with luminal impression of the esophageal stent.
b CT scan of the thorax at the level of the tracheal
bifurcation showing compression of the left main bronchus (white arrows) by the
esophageal stent (black arrowheads).
Stent-related compression of the left main bronchial wall was
verified by computed tomography (CT) ([Fig. 2 b]). Therefore, endoscopic stent
removal was considered to be the only therapeutic option and was performed,
resulting in resolution of the bronchial obstruction. Although no further
variceal bleeding occurred after stent removal, 7 days later the patient died
because of liver failure.
We describe an important complication of therapeutic self-expanding
metal stent implantation for esophageal variceal bleeding. This stent consists
of a plastic-covered nitinol mesh (length 135 mm; diameter 25 mm;
proximal and distal flare 30 mm). Its high radial expansion force
enables compression of (bleeding) esophageal varices. This stabilizes the
situation for ≤ 7 days (maximum duration of use as recommended by the
manufacturer) before applying further therapeutic measures [1]. Airway malignancy is a contraindication, but bronchial
compression in an otherwise unaffected respiratory system has not been
reported. A few authors have reported rapid respiratory dysfunction after stent
placement [2]
[3]
[4], but there are no reports on specific complications
related to use of the stent described here.
We recommend careful selection of patients with respiratory
impairment, and, in case of deterioration after stent implantation, to consider
and rapidly treat airway compression, e. g. by immediate stent
removal.
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