scholarly journals Embryological Basis and Clinical Correlation of the Rare Congenital Anomaly of the Human Gall Bladder: - “The Diverticulum” - A Morphological Study

2013 ◽  
Author(s):  
Jaba Rajguru
Keyword(s):  
Congenital Anomaly ◽  
Gall Bladder ◽  
Morphological Study ◽  
Clinical Correlation ◽  
Rare Congenital Anomaly

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 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 Large duplicated gallbladder: a rare congenital anomaly

2021 ◽  
Vol 9 (7) ◽  
pp. 2117
Author(s):  
Bhimarao Patil ◽  
Rashmi M. Nagaraju
Keyword(s):  
Congenital Anomaly ◽  
Laparoscopic Surgery ◽  
Gall Bladder ◽  
Surgical Complications ◽  
Anatomical Variations ◽  
Rare Congenital Anomaly ◽  
Bladder Duplication

Gall bladder duplication is a rare congenital anomaly, which may be asymptomatic or may present with disorders similar to that of a single gall bladder. The finding is important due to its association with biliary ductal and hepatic arterial anatomical variations, which may lead to inadvertent complications during laparoscopic surgery. We present a case of duplicated gallbladder with one of the gall bladder appearing large, elongated and coiled, without signs of cholelithiasis / cholecystitis. MRCP was helpful in tracing the two cystic ducts. This case emphasizes on importance of pre-operative anatomical delineation with MRCP in unsuspecting cases in order to minimize the incidence of post surgical complications.

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 Cor triatriatum dexter, a very rare congenital anomaly presented in a complex pathological context – case presentation

2014 ◽  
Vol 60 (4) ◽  
pp. 160-162
Author(s):  
Liliana Gozar ◽  
Cristina Blesneac ◽  
Rodica Toganel
Keyword(s):  
Congenital Anomaly ◽  
Cytomegalovirus Infection ◽  
Cor Triatriatum ◽  
Anatomical Feature ◽  
Renal Anomalies ◽  
Anatomical Variant ◽  
Case Presentation ◽  
Congenital Cytomegalovirus ◽  
Rare Congenital Anomaly ◽  
Cor Triatriatum Dexter

Abstract Background Cor triatriatum dexter is an extremely rare congenital anomaly, and in most cases, without hemodynamic significance. Congenital cytomegalovirus infection is the most common viral infection, the majority of infected infants being asymptomatic and only 5-15% being symptomatic in the neonatal period. Case report We present the case of a female infant, aged 3 months. Clinical examination reveals cranial and facial anomalies. The karyotype was normal. Laboratory tests revealed the presence of anti-CMV antibodies in urine. Imaging studies showed cerebral and renal anomalies. Echocardiographic exam revealed a congenital anatomical feature without hemodynamic significance - cor triatriatum dexter. Conclusions although cytomegalovirus infection is mostly asymptomatic, it can present as a complex pathological association, in which a congenital cardiac anatomical feature without hemodynamic significance, considered by some authors as an anatomical variant, can appear

scholarly journals Roberts uterus: a rare congenital anomaly

2017 ◽  
Vol 6 (12) ◽  
pp. 5657
Author(s):  
Nagendra Sardeshpande ◽  
Pratima Chipalkatti ◽  
Jainesh Doctor
Keyword(s):  
Congenital Anomaly ◽  
Abdominal Pain ◽  
Adnexal Mass ◽  
Lower Abdominal Pain ◽  
Uterine Horn ◽  
Transabdominal Ultrasound ◽  
Septate Uterus ◽  
Bicornuate Uterus ◽  
Rare Congenital Anomaly ◽  
Hysteroscopic Resection

A 23-year-old girl presented with severe cyclical lower abdominal pain during menstruation since menarche, which had increased since the last 4 years. Transabdominal ultrasound showed adnexal mass with no internal vascularity; MRI reported it as bicornuate uterus with one non-communicating right uterine horn with haematometra. On hysteroscopy there was evidence of septate uterus communicating only to the left ostia. Ultrasonography-guided hysteroscopic resection of septa with drainage of haematometra was done. Patient is presently asymptomatic.

CONGENITAL METACARPAL SYNOSTOSIS TREATED BY DOUBLE BONE BLOCKS TECHNIQUE: A CASE REPORT FROM THAILAND

Hand Surgery ◽  
2005 ◽  
Vol 10 (01) ◽  
pp. 131-134 ◽  
Author(s):  
Surut Jianmongkol ◽  
Tala Thammaroj ◽  
Kitiwan Vipulakorn
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Surgical Techniques ◽  
Rare Condition ◽  
Rare Congenital Anomaly

Congenital metacarpal synostosis is a rare congenital anomaly in the hand, especially in our area. There were several reports of surgical techniques for correction deformities. We report this rare condition in our hospital and treatment with the metacarpal osteotomy and double bone blocks technique of grafting.

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