Dyskeratosis Congenita Complicated by Hepatic Fibrosis With Hepatic Vein Thrombosis

被引:4
作者
Yoshida, Hideki [1 ]
Imamura, Toshihiko [1 ]
Sakamoto, Kenichi [1 ]
Asai, Daisuke [1 ]
Nakatani, Takuya [2 ]
Morimoto, Akira [3 ]
Hosoi, Hajime [1 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Pediat, Kyoto 6028566, Japan
[2] Matsushita Mem Hosp, Dept Pediat, Osaka, Japan
[3] Jichi Med Univ, Dept Pediat, Shimotsuke, Tochigi, Japan
关键词
dyskeratosis congenita; hepatic complication; telomere; danazol; MUTATIONS; DANAZOL; DISRUPTION; TERT;
D O I
10.1097/MPH.0000000000000001
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
We describe the case of 2 male siblings with dyskeratosis congenita (DC). Extensive genetic analysis failed to identify a causative genetic abnormality. The elder brother developed hepatic fibrosis accompanied with hepatic vein thrombosis at the age of 9 years. Recent studies have found that patients with DC sometimes develop hepatic complications, including cirrhosis. However, little is known about hepatic complications in patients with DC who lack these mutations. Further genetic studies are required to understand the relationship between DC and hepatic complications. In addition, although danazol can sometimes be effective for treating bone marrow failure, hepatotoxicity can be a major complication. Therefore, when danazol is administered to patients with DC, careful monitoring for hepatic complications is important.
引用
收藏
页码:308 / 311
页数:4
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