2024-03-29T05:37:16Z
https://u-ryukyu.repo.nii.ac.jp/oai
oai:u-ryukyu.repo.nii.ac.jp:02015760
2022-10-31T07:43:57Z
1642838163960:1642838198944:1642838233003:1642838238373
1642838403551:1642838412624
[症例報告]肝サルコイドーシス3例についての検討
Three cases of hepatic sarcoidosis
上原, 正照
佐久川, 廣
川木, 忠仁
下地, 克佳
嘉手納, 啓三
金城, 福則
浦崎, 政仁
安座間, 聡
小張一峰
Uehara, Masaaki
Sakugawa, Hiroshi
Kawaki, Tadahito
Shimoji, Katsuyoshi
Kadena, Keizo
Kinjo, Fukunori
Urasaki, Masahito
Azama, Satoshi
Kobari, Kazumine
サルコイドーシス
門脈圧亢進症
肉芽腫
Sarcoidosis is a multisystem granulomatous disorder of unknown etiology involving various organs. Hilar adenopathy, pulmonary parenchymal infiltration and skin or eye lesions are the most common presentations, and also in liver granuloms are frequently found. However, usually no evidence of hepatic cellular dysfunction is observed in the beginning of the disease. In the paper it was reported that three cases of sarcoidosis revealed the clinical manifestation of liver dysfunction, ascites and other sings of portal hypertension, and these symtoms could be clues of the diagnosis of sarcoidosis.
論文
http://purl.org/coar/resource_type/c_6501
琉球大学医学部
Faculty of Medicine, University of the Ryukyus
1986
VoR
0289-1530
AN10027430
琉球大学医学会雑誌 : 医学部紀要 = Ryukyu medical journal
1
9
74
64
jpn
open access
琉球医学会