scholarly journals A Case of Double Gallbladder with Adenocarcinoma Arising from the Left Hepatic Duct: A Case Report and Review of the Literature

2010 ◽  
Vol 2010 ◽  
pp. 1-6 ◽  
Author(s):  
Masahiro Kawanishi ◽  
Yukio Kuwada ◽  
Yutaka Mitsuoka ◽  
Shogo Sasao ◽  
Teruo Mouri ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Hepatic Duct ◽  
Review Of The Literature ◽  
Endoscopic Retrograde ◽  
Left Hepatic Duct ◽  
Rare Congenital Anomaly ◽  
Open Laparotomy ◽  
Double Gallbladder ◽  
Biliary Anomaly

Double gallbladder is a rare congenital biliary anomaly, but an accessory gallbladder arising from the left hepatic duct is a more remarkably rare congenital anomaly. We report a case of double gallbladder with adenocarcinoma and gallstones, which was preoperatively diagnosed by endoscopic retrograde cholangiopancreatography (ERCP) and then confirmed by open laparotomy. A review of the literature is presented.

Aplasia of the Epiglottis: A Rare Congenital Anomaly

1998 ◽  
Vol 77 (1) ◽  
pp. 51-55 ◽  
Author(s):  
Jose A. Bonilla ◽  
Michael P. Pizzuto ◽  
Linda S. Brodsky
Keyword(s):  
Heart Failure ◽  
Computed Tomography ◽  
Congenital Anomaly ◽  
Obstructive Sleep Apnea ◽  
Case Report ◽  
Clinical Course ◽  
Embryological Development ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
Obstructive Sleep

Aplasia of the epiglottis is a rare laryngeal anomaly. We present a case of absence of the epiglottis in a child whose clinical course has been followed for nine years. She required a tracheostomy at two years of age for obstructive sleep apnea which resulted in heart failure; she was eventually decannulated at age seven. This case report highlights the clinical challenges faced in the identification and treatment of the sequelae of this defect. Both endoscopic and computed tomography (CT) documentation are provided. Embryological development and a review of the literature are also discussed.

scholarly journals Unusual Variant of Coronal Bladder Duplication Associated with Glans Diphallia: A Case Report and Review of the Literature

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Reza Khorramirouz ◽  
Amin Bagheri ◽  
Abdol-Mohammad Kajbafzadeh
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Coronal Plane ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
Bladder Duplication ◽  
Unusual Variant ◽  
Complete Duplication

Bladder duplication is a rare congenital anomaly which occurs in the sagittal or coronal plane and it can be associated with other anomalies. It has been previously classified as complete duplication of the bladder and urethra or incomplete duplication with two bladders and common urethra. However, complete duplication of bladder with a single urethra has been rarely reported. Herein, we present a patient with a different variation of bladder duplication in the coronal plane with two urethras originating from the main bladder and associated glans diphallia.

scholarly journals Primary Neuroendocrine Tumor of the Left Hepatic Duct: A Case Report with Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Ajay H. Bhandarwar ◽  
Taher A. Shaikh ◽  
Ashok D. Borisa ◽  
Jaydeep H. Palep ◽  
Arun S. Patil ◽  
...  
Keyword(s):  
Standard Treatment ◽  
Hepatic Duct ◽  
Surgical Excision ◽  
Diagnostic Tools ◽  
Good Survival ◽  
Review Of The Literature ◽  
Endoscopic Retrograde ◽  
Left Hepatic Duct ◽  
Histopathologic Diagnosis ◽  
Rare Malignancy

Primary Biliary Tract Neuroendocrine tumors (NET) are extremely rare tumors with only 77 cases been reported in the literature till now. We describe a case of a left hepatic duct NET and review the literature for this rare malignancy. To the best of our knowledge the present case is the first reported case of a left hepatic duct NET in the literature. In spite of availability of advanced diagnostic tools like Computerized Tomography (CT) Scan and Endoscopic Retrograde Cholangio Pancreaticography (ERCP) a definitive diagnosis of these tumors is possible only after an accurate histopathologic diagnosis of operative specimens with immunohistochemistry and electron microscopy. Though surgical excision remains the gold standard treatment for such tumors, patients with unresectable tumors have good survival with newer biologic agents like Octreotride.

Ectrodactyly-ectodermal dysplasia-clefting syndrome

2000 ◽  
Vol 90 (9) ◽  
pp. 460-464 ◽  
Author(s):  
GJ Kelman ◽  
RC Aronoff
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Female Patient ◽  
Surgical Management ◽  
Ectodermal Dysplasia ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
Rare Syndrome ◽  
Clinical Triad ◽  
Musculoskeletal Involvement

Ectrodactyly-ectodermal dysplasia-clefting syndrome is a rare congenital anomaly that affects tissues of mesodermal and ectodermal origin. Musculoskeletal involvement frequently requires orthopedic intervention. The authors present a review of the literature pertaining to this rare syndrome as well as a case report of a female patient who exhibited the complete clinical triad. A description of the surgical management of her condition is also presented.

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.

Supernumerary intrathoracic rib, a rare congenital anomaly: Case report and review of the literature

2020 ◽  
Vol 55 (6) ◽  
pp. 1487-1489
Author(s):  
Eleanor D. Muise ◽  
Edward Y. Lee ◽  
Harriet J. Paltiel ◽  
Jonathan M. Gaffin
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly

Supernumerary Nostril with Complete Unilateral Cleft Lip: A Case Report and Review

2007 ◽  
Vol 44 (6) ◽  
pp. 657-659 ◽  
Author(s):  
Rajesh S. Powar ◽  
Vijay R. Tubaki
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Cleft Palate ◽  
Cleft Lip ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
First Case ◽  
The World ◽  
Supernumerary Nostril

The supernumerary nostril is an extremely rare congenital anomaly of duplication. A review of the literature shows that only 17 cases have been reported in the world. The supernumerary nostril in association with facial clefting is even more rare, with only three cases reported so far. We are reporting a case of supernumerary nostril in association with complete unilateral cleft lip without cleft palate, which happens to be the first case of its kind to be reported. Most supernumerary nostrils are situated superior to the normal nostrils and very few of them are situated at the same level or below the normal nostrils. In this case, the supernumerary nostril was placed lateral to the normal nostril.

scholarly journals Anterior sacral meningocele complicated by rectothecal fistula and rectorrhea: A Case report and review of the literature

2020 ◽  
Vol 11 ◽  
pp. 117
Author(s):  
Abolfazl Rahimizadeh ◽  
Saeed Ehteshami ◽  
Ava Rahimizadeh ◽  
Mona Karimi
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Posterior Approach ◽  
Case Description ◽  
Review Of The Literature ◽  
Rare Congenital Anomaly ◽  
Surgical Closure ◽  
Anterior Sacral Meningocele

Background: Anterior sacral meningocele (ASM) is a rare congenital anomaly. It is characterized by herniation of the dura through a defect in the anterior sacrum. Rarely, however, it may extend to the rectal area through a rectothecal fistula with or without rectorrhea. Case Description: Here, we present a case of ASM associated with a rectothecal fistula and rectorrhea. Surgical closure of the ostium of the cyst through a posterior approach resulted in long-term improvement Conclusion: An ASM with both rectothecal fistula and rectorrhea is extremely rare.

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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