论文信息 - Familial haemophagocytic lymphohistiocytosis in two newborn siblings: a good mimicker of newborn sepsis - 字舞流文

Familial haemophagocytic lymphohistiocytosis in two newborn siblings: a good mimicker of newborn sepsis

Abstract Familial haemophagocytic lymphohistiocytosis (FHL) is a rare, autosomal recessive disorder. We report two newborn siblings diagnosed as FHL.

N. Yaralı | A. Zenciroğlu | A. Metin | N. Demirel | A. Baş

[1] G. Janka. Familial and acquired hemophagocytic lymphohistiocytosis , 2006, European Journal of Pediatrics.

[2] H. Hennies,et al. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A , 2006, Human mutation.

[3] S. Ohga,et al. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences. , 2005, Critical reviews in oncology/hematology.

[4] L. Mouthon,et al. Pathogenesis of hemophagocytic syndrome (HPS). , 2004, Autoimmunity reviews.

[5] R. Egeler,et al. Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation. , 2002, Blood.

[6] A. Sherbany,et al. Hemophagocytic lymphohistiocytosis presenting with thrombocytopenia in the newborn. , 2002, Journal of pediatric hematology/oncology.

[7] Marion E. Schneider,et al. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis. , 2001, American journal of human genetics.

[8] A. Fischer,et al. Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society. , 1996, Leukemia.

[9] A. Öst,et al. DIAGNOSTIC GUIDELINES FOR HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS , 1991 .