Lymphohistiocytic activation syndrome and Burkholderia cepacia complex infection in a child revealing chronic granulomatous disease and chromosomal integration of the HHV-6 genome;Syndrome d'activation lymphohistiocytaire associé àune infection à Burkholderia cepacia complex chez un nourrisson révélant une granulomatose septique et une intégration génomique du virus HHV-6

Archives de Pediatrie

Volumn 18, Issue 4, 2011, Pages 416-419

  Araujo, A ^a   Pagnier, A ^a   Frange, P ^b   Wroblewski, I ^a   Stasia, M J ^a   Morand, P ^a   Plantaz, D ^a  

^a GRENOBLE UNIVERSITY HOSPITAL   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BONE MARROW TRANSPLANTATION; BURKHOLDERIA CEPACIA COMPLEX; BURKHOLDERIA CEPACIA INFECTION; CASE REPORT; CHROMOSOME; CHRONIC GRANULOMATOUS DISEASE; HERPES VIRUS INFECTION; HUMAN; HUMAN HERPESVIRUS 6; INFANT; LYMPHOHISTIOCYTIC ACTIVATION SYNDROME; MALE; MULTIPLE ORGAN FAILURE; SYNDROME; VIRUS DNA CELL DNA INTERACTION; VIRUS GENOME;

BURKHOLDERIA CEPACIA; BURKHOLDERIA INFECTIONS; DNA, VIRAL; EXANTHEMA SUBITUM; GRANULOMATOUS DISEASE, CHRONIC; HERPESVIRUS 6, HUMAN; HISTIOCYTOSIS; HUMANS; INFANT; MALE; SYNDROME; VIRUS INTEGRATION;

EID: 79953087914     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2011.01.006     Document Type: Article

References (15)

1. Segal B.H., Leto T.L., Gallin J.I., et al. Genetic, biochemical, and clinical features of chronic granulomatous disease. Medicine (Baltimore) 2000, 79:170-200.
2. Stasia M.J., Cathebras P., Lutz M.F., et al. La granulomatose septique chronique. Rev Med Int 2009, 30:221-232.
3. Winkelstein J.A., Marino M.C., Johnston R.B., et al. Chronic granulomatous disease. Report on a national registry of 368 patients. Medicine (Baltimore) 2000, 79:155-169.
4. Stephan J.L., Galambrun C. Syndrome d'activation lymphohistiocytaire chez l'enfant. Arch Pediatr 2000, 7:278-286.
5. Karras A., Hermine O. Syndrome d'activation macrophagique. Rev Med Interne 2002, 23:768-778.
6. Stephan J.L. Syndromes hémophagocytaires et déficits immunitaires primitifs. Arch Pédiatr 2003, 10(Suppl. 4):517-520.
7. Mahenthiralingam E., Urban T.A., Goldberg J.B. The multifarious, multireplicon Burkholderia cepacia complex. Nat Rev Microbiol 2005, 3:144-156.
8. Sirinavin S., Techasaensiri C., Pakaksama S., et al. Hemophagocytic syndrome and Burkholderia cepacia splenic microabscesses in a child with chronic granulomatous disease. Pediatr Infect Dis J 2004, 23:882-884.
9. Hisano M., Sugawara K., Tatsuzawa O., et al. Bacteria-associated haemophagocytic syndrome and septic pulmonary embolism caused by Burkholderia cepacia complex in a woman with chronic granulomatous disease. J Med Microbiol 2007, 56:702-705.
10. Yamanishi K., Okuno T., Shikari K., et al. Identification of human herpes virus 6 as a causal agent for exanthem subitum. Lancet 1988, 1:1065-1067.
11. Lusso P. Human herpesvirus 6 (HHV-6). Antivir Res 1996, 31:1-21.
12. Leong H.N., Tuke P., Tedder R., et al. The prevalence of chromosomally integrated human herpesvirus 6 genomes in the blood of UK blood donors. J Med Virol 2007, 145-151.
13. Ward K.N., Leong H.N., Thiruchelvam A.D., et al. Human herpesvirus 6 DNA levels in cerebrospinal fluid due to primary infection differ from those due to chromosomal viral integration and have implications for diagnosis of encephalitis. J Clin Microbiol 2007, 45:1298-1304.
14. Breese Hall C., Caserta M., Schnabel K., et al. Chromosomal integration of human herpesvirus 6 is the major mode of congenital human herpesvirus 6 infection. Pediatrics 2008, 122:513-520.
15. Daibata M., Taguchi T., Nemoto Y., et al. Inheritance of chromosomally integrated human herpesvirus 6 DNA. Blood 1999, 94:1545-1549.