Primary hemophagocytic lymphohistiocytosis in Turkish children

Pediatric Hematology and Oncology

Volumn 20, Issue 5, 2003, Pages 367-371

  Gürgey, Aytemiz ^a   Gogus S ^a   Ozyurek E ^a   Aslan, D ^a   Gumruk F ^a   Cetin M ^a   Yuce A ^a   Ceyhan, M ^a   Secmeer G ^a   Yetgin, S ^a   Hicsonmez G ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Familial lymphohistiocytosis; Hemophagocytic lymphohistiocytosis; Sporadic lymphohistiocytosis

Indexed keywords

LACTATE DEHYDROGENASE;

ARTICLE; AUTOPSY; BONE MARROW BIOPSY; CHILD; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; HEMOPHAGOCYTIC SYNDROME; HEREDITY; HUMAN; INFANT; PRIMARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SPLEEN BIOPSY; TURKEY (REPUBLIC);

EID: 10744221563     PISSN: 08880018     EISSN: None     Source Type: Journal    
DOI: 10.1080/08880010390203891     Document Type: Article

References (14)

1. Janka GE. Familial hemophagocytic lymphohistiocytosis. Eur J Pediatr. 1983;140:221-230.
2. Henter JI, Arico M, Elinder G, Imashuku S, Janka GE. Familial hemophagocytic lymphohistiocytosis: primary hemophagocytic lymphohistiocytosis. Hematol Oncol Clin North Am. 1998;12:417-433.
3. Henter JI, Elinder G, Söder O, Hansson M, Andersson B, Andersson U. Hypercytokinemia in familial hemophagocytic lymphohistiocytosis. Blood. 1991;78:2918-2922.
4. Fujiwara F, Hibi S, Imashuku S. Hypercytokinemia in hemophagocytic syndrome. Am J Pediatr Hematol Oncol. 1993;15:92-98.
5. Fisman DN. Hemophagocytic syndromes and infection. Emerg Infect Dis. 2000;6:601-608.
6. Hicsönmez G, Özme Ş, Bektaş S. Syndrome mimicking histiocytic medullary reticulosis due to diphenylhydantoin therapy. Turk J Pediatr. 1980;22:28-31.
7. Lichtenheld MG, Podack ER. Structure of the human perforin gene: a simple gene organization with interesting potential regulatory sequences. J Immunol. 1989;143:4267-4274.
8. Stepp SE, Dufourcq-Lagelouse R, Le Deist F, et al. Perforin gene defects in familial hemophacytic lymphohistiocytosis. Science. 1999;286:1957-1959.
9. Goransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, et al. Spectrum of perform gene mutations in familial hemophagocytic lymphohistiocytosis. Am J Hum Genet. 2001;68:590-597.
10. Henter JI, Elinder G, Ost A, and the FHI Study Group of the Histiocyte Society. Diagnostic guidelines for hemophagocytic lymphohistiocytosis. Semin Oncol. 1991;18:29-33.
11. Henter JI, Elinder G, Soder O, Ost A. Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis. Acta Pediatr Scand. 1991;80:428-435.
12. Imashuku S, Hibi S, Todo S. Hemophagocytic lymphohistiocytosis in infancy and childhood. J Pediatr. 1997;130:352-357.
13. Henter JI, Elinder G. Cerebromeningeal hemophagocytic lymphohistiocytosis. Lancet. 1992;339 (8785):104-107.
14. Allen M, De Fusco C, Legrand F, et al. Familial hemophagocytic lymphohistiocytosis: how late can the onset be? Haematologica. 2001;86:499-503.