scholarly journals A Case Report of Hepatocellular Carcinoma Associated with Gastric Cancer in a Young Patient with Myotonic Dystrophy

2014 ◽  
Vol 75 (10) ◽  
pp. 2909-2916 ◽  
Author(s):  
Shingo SHIMADA ◽  
Kazuhiro OGASAWARA ◽  
Tokushi KOBAYASHI ◽  
Tomoaki KAWAI ◽  
Seiji KOBAYASHI ◽  
...  
2016 ◽  
Vol 77 (5) ◽  
pp. 1271-1276 ◽  
Author(s):  
Kenji UMEDA ◽  
Ryuichi KUMASHIRO ◽  
Yasuhiro HIRABAYASHI ◽  
Toshio BANDO ◽  
Tohru UTSUNOMIYA

1999 ◽  
Vol 60 (7) ◽  
pp. 1960-1963
Author(s):  
Masatoshi ISHIZAKI ◽  
Norio AKIYAMA ◽  
Kiyotaka OSAWA ◽  
Koichiro FUJITA ◽  
Hiroyuki SUGIYAMA ◽  
...  

2018 ◽  
Vol 2 ◽  
pp. 5
Author(s):  
Scott P Patterson ◽  
Richard G Foster

This case report describes the chemoembolization of a small hepatocellular carcinoma employing a lipiodol drug delivery system utilizing a novel arterial pathway. Because the target lesion was precariously located adjacent to the inferior heart border and the diaphragm, it was unsuitable for imaging-guided microwave ablation. To achieve chemoembolization, several intraprocedural adaptations were necessary, given the variant anatomy encountered and difficulty accessing the left gastric artery through a celiac artery approach. The left gastric artery was selected from a superior mesenteric artery approach through the pancreaticoduodenal arcade (Rio Branco’s arcade). This case illustrates the importance of a mastery of the vascular anatomy and variants of hepatic arterial flow.


Author(s):  
И.А. Синельникова ◽  
И.В. Сопрунова ◽  
О.П. Николаева

В статье представлено описание семейного случая миотонической дистрофии Россолимо-Штейнерта-Куршмана-Баттена. Диагноз подтвержден в результате ДНК-диагностики: выявлено увеличенное число копий CTG-повтора гена DMPK, ответственного за развитие миотонической дистрофии. A family case report of Rossolimo-Steinert-Curschmann myotonic dystrophy is presented. An increased number of copies of CTG-repeats of the DMPK gene responsible for the development of MD, i.e., the diagnosis was confirmed by molecular genetic method.


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