Mineshita M, Kayashima S, Makishima M, Kimura F, Sasaki T, Takagi S, Matuura Y, Shimomura S, Yamamoto K, Satou N
Third Department of Internal Medicine, National Defense Medical College.
Rinsho Ketsueki. 1992 Jan;33(1):30-5.
A 36-year-old woman with disseminated intravascular coagulation syndrome (DIC) was admitted to the Third Department of Internal Medicine of the National Defense Medical College Hospital. Even after she recovered from DIC, she had a low level of C1-inactivator. Her past history, family history and family study revealed that she and her family showed hereditary angioneurotic edema (HANE). There have been no reports of HANE associated with DIC. She had two HANE attacks after discharge. We used nafamostat mesilate, a strong inhibitor of activated first complement component, to treat the attacks. She obtained subjective relief and her serological data were improved. Nafamostat mesilate was considered effective for HANE attack.
一名患有弥散性血管内凝血综合征(DIC)的36岁女性入住国防医科大学附属医院内科第三病房。即便她从DIC中康复后,其C1抑制物水平仍较低。她的既往史、家族史及家族研究显示,她及其家族患有遗传性血管性水肿(HANE)。此前尚无HANE与DIC相关的报道。出院后她发生了两次HANE发作。我们使用甲磺酸萘莫司他,一种活化的第一补体成分的强效抑制剂,来治疗发作。她获得了主观缓解,血清学数据也有所改善。甲磺酸萘莫司他被认为对HANE发作有效。