M. Ibrarullah et al., MIRIZZIS SYNDROME - IDENTIFICATION AND MANAGEMENT STRATEGY, Australian and New Zealand journal of surgery, 63(10), 1993, pp. 802-806
Fourteen cases of Mirizzi's syndrome are presented here. Clinical pres
entation was pain (14), jaundice (14), fever (10) and peritonitis (1).
A clinical diagnosis of choledocholithiasis was considered in all the
patients. Pre-operative diagnosis of Mirizzi's syndrome was made in f
ive patients on the basis of cholangiogram and the remaining cases wer
e diagnosed at surgery. The stage (type) of Mirizzi's syndrome was bas
ed on the extent of erosion of the common bile duct. Four patients had
type I, seven type II and three type III lesions. Associated choledoc
holithiasis was present in five and acute free perforation of the gall
-bladder in one. The operative procedures performed were partial chole
cystectomy for type I, partial cholecystectomy, choledochoplasty and T
-tube choledochostomy for type II and bilioenteric anastomosis for typ
e III lesions. Two patients had retained common bile duct stones. Mean
follow up was 14 months (range 1-27 months). One patient with seconda
ry biliary cirrhosis continues to have persistently elevated serum alk
aline phosphatase levels without any demonstrable biliary obstruction.
Diagnostic and operative strategies are discussed and a follow up pro
tocol for such patients is suggested.