Case Report: Hemophagocytic Lymphohistiocytosis Secondary to Plasmodium ovale wallikeri Infection

被引:2
|
作者
Novella-Mena, Maria [1 ]
Cantudo-Munoz, Purificacion [2 ]
Tallon-Perez, Jose David [3 ]
del Mar Gomez-Rodriguez, Maria [4 ]
Rojo-Marcos, Gerardo [1 ,5 ,6 ]
机构
[1] Hosp Univ Principe Asturias, Med Interna, Alcala De Henares, Madrid, Spain
[2] Hosp Univ San Agustın, UGC Lab Anal Clin, Microbiol & Parasitol Clın, Linares, Jaen, Spain
[3] Hosp Univ San Agustin, Hematol & Hemoterapia, UGC Hematol & Hemoterapia, Linares, Jaen, Spain
[4] Hosp Univ San Agustın, UGC Med Interna, Med Interna, Linares, Jaen, Spain
[5] Univ Alcala, Alcala De Henares, Madrid, Spain
[6] Prıncipe Asturias Univ Hosp, Ctra Meco S-N, Alcala De Henares 28805, Madrid, Spain
来源
关键词
D O I
10.4269/ajtmh.23-0180
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
We report the first known case of hemophagocytic lymphohistiocytosis (HLH) secondary to imported Plasmodium ovale wallikeri infection in a 58-year-old white woman. A delayed diagnosis of malaria and HLH was made after protracted fever and pancytopenia failed to respond adequately to antimalarial treatment, which required intravenous methylprednisolone and gamma-globulin therapy to resolve.
引用
收藏
页码:608 / 610
页数:3
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