Una rara complicanza dell’ERCP: la sindrome di Mallory-Weiss Ann. Ital. Chir., 76, 2, 2005 199 Ann


COD: 199-202 Categorie: ,

Carmelo Sciumè, Girolamo Geraci, Franco Pisello, Francesco Li Volsi, Tiziana Facella, Michele Frazzetta, Dario Raimondo, Paolo Passariello, Giuseppe Modica

Ann. Ital. Chir., 2005; 76: 199-202

La mia nuova descrizione qui!

Price of a print issue €25.00

OBJECTIVE: To describe the management and outcome after endoscopic treatment of hematemesis by Mallory-Weiss Syndrome
(MWS) occurred after CPRE (suspected choledocolithiasis).
BACKGROUND DATA: Although cough and retching is common during EGD or CPRE, MWS resulting from endoscopy
seems to be uncommon (0.0001-0.04%) and always self-limiting.
CASE REPORT: The patient was submitted to CPRE with the suspicion of choledocholithiasis. Eight hours after CPRE
the patient presented with hematemesis amd hypotension. With emergency EGD, the AA identified a small bleeding
mucosal tear (visible vessel with spurting) just proximal to the esophagogastric junction. The patient was safely treated
with endoscopic hemoclipping after the failure of sclerotherapy.
CONCLUSIONS: The usefulness of hemoclipping in MWS is emphasized: although always self-limiting, endoscopic hemostasis
is mandatory in high risk patients.
The hemoclips are effective and safe in hemostasis in the case of bleeding visible vessel (spurting or oozing), even with
or after sclerotherapy. The hemoclips not obstacles the healing.