Case of muscle abscess due to disseminated nocardiosis in a patient with autoimmune hemolytic anemia, and review of the published work

被引:4
作者
Ukai, Yoshiko [1 ]
Fujimoto, Noriki [1 ]
Fujii, Norikazu [1 ]
Shirai, Masae [1 ]
Wakabayashi, Makiko [1 ]
Uenishi, Toshiaki [1 ]
Koizumi, Yusuke [2 ]
Hodohara, Keiko [2 ]
Shimizu, Kaoru [3 ]
Tanaka, Toshihiro [1 ]
机构
[1] Shiga Univ Med Sci, Dept Dermatol, Otsu, Shiga 5202192, Japan
[2] Shiga Univ Med Sci, Dept Internal Med Hematol, Shiga, Japan
[3] Shiga Univ Med Sci, Dept Clin Lab, Shiga, Japan
关键词
autoimmune hemolytic anemia; disseminated nocardiosis; muscle abscess; Nocardia farcinica; PSOAS ABSCESS; CASE SERIES; INFECTION; FARCINICA;
D O I
10.1111/j.1346-8138.2011.01393.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Although disseminated nocardiosis has been increasing with the expansion of immunosuppressive therapy and improvement in diagnostic methods, muscle abscess is a rare complication. There have been only nine case reports of muscle abscess due to Nocardia infection in the English-language published work. We present a case of muscle abscess with disseminated nocardiosis, and review the published work. The patient had been taking prednisolone at 20 mg a day for autoimmune hemolytic anemia for 14 years. She presented with erythema on her thigh resembling cellulitis. Computed tomography showed muscle abscess. The isolated organism was identified as Nocardia farcinica employing polymerase chain reaction and antibiotic sensitivity testing. The diagnosis of muscle abscess due to nocardiosis can be easily missed because there are no characteristic symptoms.
引用
收藏
页码:466 / 469
页数:4
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