scholarly journals A rare case of double gall bladder: a case report and review of literature

2021 ◽  
Vol 8 (11) ◽  
pp. 3488
Author(s):  
Gurushantappa Yalagachin ◽  
Abhijit D. Hiregoudar ◽  
Ashika Bagur ◽  
Abhishek Choudhari
Keyword(s):  
Congenital Anomaly ◽  
Laparoscopic Cholecystectomy ◽  
Case Report ◽  
Gall Bladder ◽  
Preoperative Diagnosis ◽  
Rare Case ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Hepatobiliary System ◽  
Double Gallbladder

Double gall bladder is a rare congenital anomaly of the Hepatobiliary system with an incidence of 1:4000 due to abnormalities resulting during the embryogenesis during fourth to sixth week of gestation. Boyden was first to describe the duplication of the gallbladder and Harlaftis classification describes three types for the duplication of the gallbladder. Preoperative diagnosis of the duplication of the gallbladder has to be confirmed to minimise the complications during the surgery and post operatively. Sometimes the duplication of the gallbladder is missed preoperatively and hence increasing the risk and complications during the cholecystectomy. MRCP is the investigation of choice for preoperative diagnosis of the duplication and the laparoscopic cholecystectomy being the treatment of choice for the double gallbladder. We encountered a 25 year old girl with duplicate gallbladder who underwent laparoscopic cholecystectomy with removal of both gallbladders successfully.

scholarly journals Septate gall bladder: a surgical surprise with review of literature

2020 ◽  
Vol 7 (10) ◽  
pp. 3516
Author(s):  
Kaptan Singh ◽  
Atul S. Joshi ◽  
Agrawal K. Khemchand ◽  
Hariom Sheoran ◽  
Priti Rabadiya ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Laparoscopic Cholecystectomy ◽  
Postoperative Complications ◽  
Gall Bladder ◽  
Preoperative Diagnosis ◽  
Operative Procedure ◽  
Review Of Literature ◽  
First Line ◽  
Rare Congenital Anomaly ◽  
The Common

Septate gallbladder is a rare congenital anomaly, which can present a challenge for the surgeon who performs laparoscopic cholecystectomy. The common first line modality for screening in symptomatic gallbladder pathology is still ultrasonography. Preoperative diagnosis of this anomaly is not common. Pre- operative diagnosis and being acquainted with this anomaly decreases the possibility of injury to the biliary tract, the number of postoperative complications and the possible need for further surgical procedures. We present a case of septate gallbladder, which was diagnosed during the operative procedure. Despite the finding of a septate gallbladder, the performance of laparoscopic cholecystectomy was uneventful.

scholarly journals Volvulus of gall bladder: case report

2017 ◽  
Vol 4 (11) ◽  
pp. 3792 ◽  
Author(s):  
Rajneesh Kumar ◽  
Ankur Hastir ◽  
Ramandeep Singh Walia ◽  
Subhash Goyal
Keyword(s):  
Laparoscopic Cholecystectomy ◽  
Case Report ◽  
Gall Bladder ◽  
Preoperative Diagnosis ◽  
Rare Case ◽  
Rare Condition ◽  
Middle Aged ◽  
Biliary Peritonitis

Gall bladder volvulus or twisting is a rare condition and occurs due to rotation of gall bladder. Preoperative diagnosis is exception and usually misdiagnosed as cholecystitis before surgery. It is potentially fatal condition unless diagnosed and treated early leading to gangrene and biliary peritonitis. It has been reported in only about 500 cases in the literature ranging in age given 2-100 years old. We report a rare case of middle aged female 56 years old with volvulus of gall bladder having concomitant cholelithiasis treated with laparoscopic cholecystectomy.

scholarly journals Laparoscopic management of rare “ H type” duplication of gall bladder

2020 ◽  
Vol 6 (6) ◽  
pp. 354-357
Author(s):  
Dr. Anurag Mishra ◽  
◽  
Dr. Md Abu Masud Ansari ◽  
Dr. Shivanshu Misra ◽  
◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Laparoscopic Cholecystectomy ◽  
Gall Bladder ◽  
Gallstone Disease ◽  
Current Case ◽  
Rare Congenital Anomaly ◽  
Live Births ◽  
Cholecystoenteric Fistula ◽  
Double Gallbladder ◽  
Symptomatic Gallstone Disease

A duplicated gallbladder is a rare congenital anomaly with an incidence of 1:4000 live births. Theycan remain asymptomatic and identified incidentally or present as acute cholecystitis, empyema,torsion, cholecystoenteric fistula, Gall bladder lump, or carcinoma. Here the current case is aboutdiscussing a case of a 25-year-old female who presented with symptomatic gallstone disease with aduplicated gallbladder having multiple stones in both the gallbladders. MRCP performedpreoperatively revealed Y type duplication (double Gall bladder with common cystic duct).Laparoscopic cholecystectomy was performed and it finally revealed H type duplication (double Gallbladder with separate cystic ducts for each Gall Bladder).

scholarly journals Laparoscopic management of double gallbladder diagnosed intraoperatively: A case report and review of literature

2018 ◽  
Vol 87 (5-6) ◽  
Author(s):  
Jošt Kokalj ◽  
Yasmin Marianna Hunt
Keyword(s):  
Congenital Anomaly ◽  
Preoperative Diagnosis ◽  
Operative Procedure ◽  
Gall Stone ◽  
Review Of Literature ◽  
First Line ◽  
Rare Congenital Anomaly ◽  
Double Gallbladder ◽  
The Common ◽  
Gallbladder Removal

Double gallbladder is a rare congenital anomaly, which can present a challenge for the surgeon who performs laparoscopic cholecystectomies. The common first-line modality for screening in symptomatic gallbladder pathology is still ultrasonography, even though the accuracy is low. Preoperative diagnosis of this anomaly is not common as it is available in only 50 % of cases. Preoperative diagnosis and being acquainted with this anomaly decrease the possibility of injury to the biliary tract, the number of postoperative complications and the possible need for further surgical procedures.We present a case of double gallbladder which was diagnosed during the operative procedure. Based on ultrasonography screening, which showed a gall-stone in an unchanged gallbladder, a laparoscopic gallbladder removal was indicated. Despite the finding of a double gallbladder, the performance of laparoscopic gallblade removal was uneventful.

scholarly journals Bilobed gallbladder: a rare congenital anomaly of the biliary system

2021 ◽  
Vol 9 (12) ◽  
pp. 3729
Author(s):  
Pradeep Kumar Roul ◽  
Aditi Saini ◽  
Srishti Agarwal ◽  
Prashant Kumar Verma ◽  
Anjum Syed
Keyword(s):  
Congenital Anomaly ◽  
Laparoscopic Cholecystectomy ◽  
Preoperative Diagnosis ◽  
Biliary System ◽  
Additional Risk ◽  
Rare Congenital Anomaly ◽  
Time Of Surgery ◽  
Double Gallbladder

Duplication of the gallbladder is a rare congenital anomaly, which Boyden first illustrated in 1926. No additional risk of cholelithiasis or malignancy with this congenital anomaly was documented. However, this congenital anomaly is associated with more risk for complications during and after laparoscopic cholecystectomy. So, preoperative diagnosis is essential in identifying anatomical abnormalities to avoid biliary injuries at the time of surgery or the performance of an incomplete operation. The removal of an asymptomatic double gallbladder remains controversial. Here, we are reporting a case of the incidentally detected duplex gallbladder in a teenager and review the literature that will enrich the reader’s knowledge regarding this rare congenital anomaly.

scholarly journals Rare presentation of incomplete male urethral duplication: A case report and review of literature

2021 ◽  
Vol 9 (1) ◽  
pp. 292-296
Author(s):  
Orgeness J Mbwambo ◽  
Alex Mremi ◽  
Mohamed Mbarouk ◽  
Jasper Mbwambo ◽  
Frank Bright ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Postoperative Period ◽  
Surgical Removal ◽  
Urethral Duplication ◽  
Review Of Literature ◽  
Rare Presentation ◽  
Rare Congenital Anomaly ◽  
Accessory Urethra

Urethral duplication is a rare congenital anomaly affecting mainly males. Here, we report a case of urethral duplication in a 19 years old male presented as a scrotal sinus discharging pus for 1 year. Surgical removal of accessory urethra was done and postoperative period was uneventful.

scholarly journals Klippel-Feil Syndrome: A Review of Literature and Case Report

2018 ◽  
Vol 1 (1) ◽  
pp. 102-107
Author(s):  
H Mohammad ◽  
I T Annongu ◽  
D D Mue ◽  
D M Chia ◽  
R O Abah ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Clinical Presentations ◽  
Complete History ◽  
Radiological Examinations

Though Klippel-Feil syndrome is a rare congenital anomaly and the clinical presentations are varied, a complete history, physical and radiological examinations may reveal the diagnosis.

scholarly journals CASE REPORT : RARE CASE OF SMALL BOWEL OBSTRUCTION DUE TO MECKELS DIVERTICULUM

2021 ◽  
Vol 9 (06) ◽  
pp. 641-644
Author(s):  
Simranjit Kaur Dhadiala ◽  
◽  
Abhijit A. Whatkar ◽  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Small Bowel ◽  
Small Bowel Obstruction ◽  
Bowel Obstruction ◽  
Rare Case ◽  
Rare Congenital Anomaly ◽  
Meckels Diverticulum ◽  
Male To Female

Meckels diverticulum is a rare congenital anomaly of gastrointestinal tract, seen in 2% of population. It was first described by Guilhemus Fabricus Hildonus in 1598. Meckels diverticulum is an anomaly derived from incomplete obliteration of omphalo-mesenteric duct. It is rarely seen in adults, with prevalence of male to female of 2:1. Complications associated with Meckels diverticulum are hemorrhage, inflammation and intestinal obstruction. We present to you a case of 17 year old male with unusual mechanism of small bowel obstruction due to Meckels diverticulum.

scholarly journals Sirenomelia with Potter syndrome: a case report and review of literature

2019 ◽  
Vol 9 (1) ◽  
pp. 400
Author(s):  
Amrita Singh ◽  
Anupma Kumari
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Lower Extremities ◽  
Rare Condition ◽  
Variable Degree ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Mermaid Syndrome ◽  
Vascular Steal

Sirenomelia or mermaid syndrome is a rare congenital anomaly characterized by variable degree of fusion of lower extremities. Awareness to this rare condition is important for prenatal diagnosis and prognosticating the fetus. The exact etiopathogenesis is still an area of research. Two pathogenic hypotheses are the vascular steal hypothesis and the defective blastogenesis hypothesis with exceptions reported in literature.

Sign in / Sign up

Export Citation Format

Share Document