scholarly journals Langerhans cell histiocytosis confined to extrahepatic bile duct causing sclerosing cholangitis in child: a case report

2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Masakazu Murakami ◽  
Shun Onishi ◽  
Yuki Ohya ◽  
Seiichi Kawabata ◽  
Kaori Isono ◽  
...  
2010 ◽  
Vol 4 (3) ◽  
pp. 653-658 ◽  
Author(s):  
Ibrahim Hatemi ◽  
Birol Baysal ◽  
Hakan Senturk ◽  
Kemal Behzatoglu ◽  
Erol Rustu Bozkurt ◽  
...  

Cases Journal ◽  
2008 ◽  
Vol 1 (1) ◽  
Author(s):  
Khalid A Al-Anazi ◽  
Abdulrahman Alshehri ◽  
Hazza A Al-Zahrani ◽  
Fahad I Al-Mohareb ◽  
Irfan Maghfoor ◽  
...  

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Bharat Mani Banjade ◽  
Ashish Rajbhandari ◽  
Rabin Koirala ◽  
Tuhin Shah ◽  
Chitra Lal Bhattachan

Abstract Background Extrahepatic bile duct duplication is an extremely rare congenital anomaly in which two common bile ducts exist. There are five different types of this anomaly and we present an unusual variant of duplication of an extrahepatic biliary system of type Va variety. Case presentation This case report describes a 63-year-old women from rural Nepal who presented with type Va of duplicated extrahepatic bile duct, with chronic calculous cholecystitis and choledocholithiasis. She was managed with cholecystectomy with hepatic ductoplasty and hepaticojejunostomy. Conclusion A rare case of double common bile duct (type Va) complicated by choledocholithiasis, cholangitis, and chronic cholecystitis is reported here. Rare cases are sometimes overlooked by modern diagnostic techniques. Correct diagnosis helps appropriate surgical intervention.


2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Mariko Kamiya ◽  
Naoto Yamamoto ◽  
Yuto Kamioka ◽  
Hirohide Inoue ◽  
Hirokazu Yotsumoto ◽  
...  

Author(s):  
JÉSSICA ANNE PEREIRA CORRÊA ◽  
LIONEY NOBRE CABRAL ◽  
TIAGO NOVAES PINHEIRO ◽  
ELIANA BRASIL ALVES ◽  
ANGELA MARIA FERNANDES DOS SANTOS

2010 ◽  
Vol 2010 ◽  
pp. 1-3 ◽  
Author(s):  
Harpreet Singh ◽  
Satnam Kaur ◽  
P. Yuvarajan ◽  
Nishant Jain ◽  
Lalit Maini

The radiological diagnosis of osteolytic lesions of the long bones in pediatric population constitutes a challenge when the case history and clinical data are uncharacteristic. We believe that the description of few clinically and histologically proven cases to verify the existence of radiological signs useful for diagnosis may be of interest. Here, we describe a case of Langerhans' cell histiocytosis (LCH) presenting as unifocal eosinophilic granuloma of femur along with a brief review of the literature.


Sign in / Sign up

Export Citation Format

Share Document