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A case of lepromatous leprosy complicated by hemophagocytosis misdiagnosed as hemophagocytic lymphohistiocytosis.

Authors :
Zeng, Xiang-Zong
Wang, Yi-Ni
Wang, Jing-Shi
Wu, Lin
Zhang, Jia
Wei, Qing
Liu, Jian
Wang, Zhao
Source :
International Journal of Infectious Diseases. Jun2014, Vol. 23, p28-30. 3p.
Publication Year :
2014

Abstract

Summary: Leprosy is an infectious chronic granulomatous disease caused by Mycobacterium leprae. The disease mainly affects the skin, peripheral nerves, mucosa, and viscera. The World Health Organization has reported that most countries with high endemicity have reached the goal of eliminating leprosy (defined as reaching a prevalence of <1 leprosy case per 10 000 population) at the national level, after years of proactive control campaigns. The incidence of leprosy has been decreasing across the globe year by year. However, misdiagnosis happens occasionally due to the complexity of clinical manifestations and lack of physician awareness of this disease. We report a case of lepromatous leprosy complicated by hemophagocytosis misdiagnosed as hemophagocytic lymphohistiocytosis. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
12019712
Volume :
23
Database :
Academic Search Index
Journal :
International Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
96189134
Full Text :
https://doi.org/10.1016/j.ijid.2014.02.004