Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome) 英文参考文献.docVIP
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Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome) 英文参考文献
Guirat-Dhouibetal.ClinicalandMolecularAllergy2012,10:6
/content/10/1/6
CMA
CASE REPORT
OpenAccess
OralHPVinfectionandMHCclassIIdeficiency
(Astudyoftwocaseswithatypicaloutcome)
NaouelGuirat-Dhouib1*,YemenBaccar1,ImèneBenMustapha2,Moniaouederni1,SamehChouaibi1,
NadiaElFekih3,MohamedRidhaBarbouche2,BassimaFezaa3,RidhaKouki1,SlamaHmida4,FethiMellouli1and
MohamedBejaoui1
Abstract
Background:MajorhistocompatibilitycomplexclassIIdeficiency,alsoreferredtoasbarelymphocytesyndromeis
arareprimaryImmunodeficiencydisordercharacterizedbyaprofondlydeficienthumanleukocyteantigenclassII
expressionandalackofcellularandhumoralimmuneresponsestoforeignantigens.Clinicalmanifestations
includeextremesusceptibilitytoviral,bacterial,andfungalinfections.Theinfectionsbegininthefirstyearoflife
andinvolveusuallytherespiratorysystemandthegastrointestinaltract.Severemalabsorptionwithfailuretothrive
ensues,oftenleadingtodeathinearlychildhood.Bonemarrowtransplantationisthecurativetreatment.
Casereports:HerewereporttwocaseswithalateoutcomeMHCclassIIdeficiency.Theyhadalongtermhistory
ofrecurrentbronchopulmonaryandgastrointestinalinfections.Bonemarrowtransplantationcouldnotbe
performedbecausenocompatibledonorhadbeenidentified.Attheageof12years,theydevelopedoral
papillomatouslesionsrelatedtoHPV(humanpapillomavirus).ThediagnosisofHPVinfectionwasdoneby
histologicalexamination.HPVtypingperformedonthetissueobtainedatbiopsyshowedHPVtype6.Thelesions
werepartiallyremovedaftertwomonthsoflasertreatment.
Conclusions:ViralinfectionsarecommoninpatientswithMHCclassIIandremainthemaincauseofdeath.
BesideswartscausedbyHPVinfectiondonotexhibitapropensityformalignanttransformation;theycancause
greatpsychosocialmorbidity.
Casepresentations
Case 1
(0.5-1.8). Lymphocyte subsets produced thefollowing:
CD3 = 2 × 109cells/L (1.2-2.6), CD4 = 1 × 109cells/L
9
A22-year-old girl,bornfromunrelatedhealthyparents (0.65-1.5),CD8=1×10 cells/L(0.37-1.1),CD19=0.374
9
of Tunisian origin, during the neonatal period had ×10 cells/
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