scholarly journals Biliary peritonitis: Rare presentation of spontaneously ruptured choledochal cyst

2022 ◽  
Vol 19 (1) ◽  
Author(s):  
Ira Shah
HPB ◽  
2021 ◽  
Vol 23 ◽  
pp. S352
Author(s):  
N.Y. Muppalla ◽  
S. Sankar

HPB Surgery ◽  
1999 ◽  
Vol 11 (3) ◽  
pp. 163-169
Author(s):  
D. M. Kelly ◽  
P. J. O'Donnell ◽  
E. R. Howard

Pulmonary lymphangitis carcinomatosa is an unusal cause of death in a young adult. This case describes an apparently healthy young woman who presented with severe acute pancreatitis, which is a recognized complication of a choledochal cyst. Autopsy examination revealed advanced malignancy with poorly differentiated adenocarcinoma penetrating the wall of the choledochal cyst and metastatic adenocarcinoma in the lymph nodes, lungs and kidneys. This case emphasises the unusual presentation of a choledochal cyst with acute pancreatitis and the aggressive nature of malignancy associated with this congenital anomaly.


2014 ◽  
pp. 112-115
Author(s):  
Sanjay Bhasin ◽  
Tariq Azad ◽  
Nasib Digra ◽  
Mubashar Mubashar ◽  
Gopal Sharma

2021 ◽  
pp. 92-93
Author(s):  
Neelendra Yesaswy MNV ◽  
Sankar Subramanian ◽  
Niket M Shah ◽  
Suresh Kumar P

Choledochal cyst (CC) is a relative rare condition in adult population. Only 20% of CC presents in adult population, of these 80% presents with additional hepatobiliary pathology (1,2). With widespread usage of cross sectional imaging, more cysts are likely being identified incidentally in asymptomatic individuals. The development of cancer arising from cysts increases from <0.7% in first decade of life to >11.4% after 2nd decade of life. Anatomic abnormality pancreaticbiliary maljunction (PBM) is a noted etiologic factor for cyst development and even for development of cancer in cysts. We report a rare adult presentation of choledochal cyst with underlying abnormal pancreaticobiliary maljunction with gall bladder carcinoma.


2013 ◽  
Vol 11 (1) ◽  
pp. 52-54
Author(s):  
Bikash Bikram Thapa ◽  
Kunda Bikram Shah ◽  
Sushil Bahadur Rawal ◽  
Srijan Malla

Postcholecystectomy syndrome is the recurrence of symptoms after cholecystectomy. Postcholecystectomy syndrome due to a combination of cystic duct stump calculus and choledochal cyst with recurrent choledocholithiasis is a rare presentation. This is a case report of a patient who had developed recurrent common bile duct calculi despite endoscopic removal and eventully managed with Rou-en-Y Hepati cojejunostomy for having choledochal cyst 39 years postcholecstectomy. Medical Journal of Shree Birendra Hospital; Jan-June 2012/vol.11/Issue1/52-54 DOI: http://dx.doi.org/10.3126/mjsbh.v11i1.7792


2015 ◽  
pp. 710-713
Author(s):  
Atish Bansod ◽  
Sunil Lanjewar ◽  
Mahendra Kamble ◽  
Kamalkant Singh ◽  
Vaibhav Nasare ◽  
...  

F1000Research ◽  
2019 ◽  
Vol 8 ◽  
pp. 1467
Author(s):  
Rafey Abdul Rahman ◽  
Umesh Kumar Gupta

Background: Biliary peritonitis due to a ruptured choledochal cyst (CC) is a rare occurrence. The difference between bile duct perforation (BDP) and ruptured choledochal cysts continues to be a matter of debate. Simple drainage, T tube placement and cholecystostomy have been proposed as the initial treatment of choice. Definitive surgery in the form excision of the CC and hepatico-enterostomy has been described as the ideal treatment option. We report a successful management of a unique case of perforated choledochal cyst in an infant who presented with biliary peritonitis. Case report: An 8 months old female child presented with biliary peritonitis as result of spontaneous perforation of a choledochal cyst. The patient was successfully managed initially by placement of T tube in the perforated cyst followed by a T tube cholangiogram. Definitive surgery was performed 5 weeks after the initial surgery in which cyst was excised and hepatico-duodenostomy was performed. The child is currently in follow up and doing well. Conclusion: Perforated CC can present as acute abdomen sometimes having only subtle signs. In absence of any previous established diagnosis of CC and trained radiological support the condition becomes challenging to diagnose preoperatively. External T-tube drainage followed by T-tube cholangiogram can help in delineating the anatomy. Cyst excision along with hepaticoportoentersomy remains the gold standard definitive treatment.


2001 ◽  
Vol 17 (7) ◽  
pp. 549-551 ◽  
Author(s):  
V. G. Shenoy ◽  
S. A. Jawale ◽  
S. N. ◽  
B.K. Kulkarni

2020 ◽  
pp. 1-2
Author(s):  
Mohamad Safwan. A ◽  
Jithu TG ◽  
Najeeb AA ◽  
Sandeep Babu

Background: Giant inguino-scrotal hernias are unusual, and associated with duodenal perforation causing peritonitis is an extremely rare presentation. Case presentation: A 73 year old gentleman presented to the Emergency department (ED) with sudden onset of lower abdominal pain, bilious vomiting, and constipation. He had a huge right sided inguino-scrotal swelling. Computed tomography (CT) abdomen showed massive inguino-scrotal hernia containing pylorus, part of duodenum and loops of jejunum, ileum and large bowel upto descending colon as contents with signs of perforation. Labs were suggestive of sepsis. At emergency surgery, perforation of the second part of duodenum with generalized peritonitis was evident. Closure of the perforation and drainage was done as a damage control procedure and definitive hernia repair was deferred for a later period. Despite intensive-care, the patient succumbed to sepsis postoperatively. Conclusion: This is a rare presentation of duodenal perforation secondary to giant inguino-scrotal hernia causing biliary peritonitis ensuing in sepsis and death. We reviewed the literature on giant inguinal hernia, and especially those associated with duodenal perforation.


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