Literature DB >> 22011194

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

Yoshiko Ukai1, Noriki Fujimoto, Norikazu Fujii, Masae Shirai, Makiko Wakabayashi, Toshiaki Uenishi, Yusuke Koizumi, Keiko Hodohara, Kaoru Shimizu, Toshihiro Tanaka.   

Abstract

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.
© 2011 Japanese Dermatological Association.

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Year:  2011        PMID: 22011194     DOI: 10.1111/j.1346-8138.2011.01393.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  1 in total

1.  Nocardia farcinica complicating Cogan's syndrome.

Authors:  Dimos Merinopoulos; Haroon Khan; Sara Ginwalla; Suzanne Lane; Richard Watts
Journal:  Oxf Med Case Reports       Date:  2014-05-28
  1 in total

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