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Osteomyelitis in leukocyte adhesion deficiency type 1 syndrome.

作者信息

Jabbari Azad Farahzad, Ardalan Maryam, Hoseinpoor Rafati Ali, Sotoudeh Soheila, Pourpak Zahra

机构信息

Bu Ali Immunology Research Center, Mashhad University of Medical Science, Mashhad, Iran.

出版信息

J Infect Dev Ctries. 2010 Mar 29;4(3):175-8. doi: 10.3855/jidc.387.

Abstract

Leukocyte adhesion deficiency type 1 (LAD-1) is a rare, inherited immunodeficiency that affects one per million people yearly and usually presents with recurrent, indolent bacterial infections of the skin, mouth, and respiratory tract and impaired pus formation and wound healing. A 13-year-old girl diagnosed LAD-I at the age of 7 years was brought to the Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, because of a draining plaque on the left leg for 2.5 years. She had recurrent skin infections and had been treated with repeated courses of different antibiotic combinations, with temporary responses, since 5 years of age. Examination revealed a 7 x 8 cm minimally erythematous hyperpigmented plaque with multiple draining sinuses on the left leg. Tissue culture yielded Pseudomonas aeruginosa. Flow cytometry showed CD18 (18.79%), CD11a (51.59%), CD11b (18.61%) and CD11c(10.60%). A plain radiography of the left leg revealed osteomyelitis. It is highly suggested that patients diagnosed mild to moderate LAD-1 with recurrent skin infection and simultaneous weak response to conventional therapy undergo (BMT) marrow transplant to prohibit subsequent life-threatening complications.

摘要

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