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1.
Arch Pediatr ; 19(11): 1157-63, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23037586

ABSTRACT

Molluscum contagiosum (MC) is common and often numerous and recalcitrant in immunocompromised children. The response to available treatments is frequently unsatisfactory. Cidofovir is a nucleoside analog of the deoxycytidine antiviral drug approved for the intravenous treatment of cytomegalovirus retinitis in AIDS patients. We report four cases of children, 5-8 years old, who developed extensive MC in the context of chemotherapy for acute lymphoid leukemia and who were treated with a cream containing cidofovir 1%. In all patients, the lesions began to regress within 2 to 4 months. For three patients, complete regression was observed in 7 to 9 months, and the children remained clear of recurrence. For one patient, partial regression was obtained after 17 months of treatment. No side effects have been observed. Treatment of MC in immunocompromised children is difficult because the usual treatments are inappropriate. Successful use of either topically or intralesionally administered cidofovir in several virally induced cutaneous diseases has been demonstrated and recently documented in the treatment of MC in immunocompromised adults. Conversely, its use in children is not documented. Although intravenous use of cidofovir may lead to severe adverse effects, one single case of a systemic side effect has been reported after topical use at a greater concentration, but no changes in laboratory data were observed. Topical cidofovir offers an effective and well-tolerated therapeutic alternative option for the treatment of MC in immunosuppressed children.


Subject(s)
Antiviral Agents/administration & dosage , Cytosine/analogs & derivatives , Molluscum Contagiosum/drug therapy , Opportunistic Infections/drug therapy , Organophosphonates/administration & dosage , Administration, Topical , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Child , Child, Preschool , Cidofovir , Combined Modality Therapy , Cryosurgery , Cytosine/administration & dosage , Female , Follow-Up Studies , Humans , Male , Molluscum Contagiosum/chemically induced , Opportunistic Infections/chemically induced , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy
2.
Int J Lab Hematol ; 32(3): 288-98, 2010 Jun.
Article in English | MEDLINE | ID: mdl-19793113

ABSTRACT

The DNA index (DI) is a prognostic factor in childhood acute lymphoblastic leukemia (ALL). The accuracy of DI measurement is important for treatment stratification: hyperdiploidy with DI > or = 1.16 is predictive of favorable prognosis whereas hypodiploidy is associated with poor prognosis. The aim of this study was to validate the accuracy of the DI measured by flow cytometry (FCM) by comparison with the karyotype. From samples of 112 childhood ALL, we created a formula to calculate a theoretical DNA index (tDI) based on the blast cell karyotype, taking into account the additional or missing chromosome material of the major clone. FCM DI correlated with tDI calculated from karyotype (R = 0.987) and with modal chromosome number (DI = 0.0202 x Modal NB + 0.0675 and R = 0.984). In three cases a hypodiploid blast cell population was detected by FCM, while only the duplicated clone was identified by the karyotype. The strong correlation between tDI and DI validates the accuracy of FCM quantification, which is technically fast on fresh or frozen samples. If the karyotype is essential to analyze chromosomal abnormalities, FCM provides complementary information in aneuploid ALLs, either by confirming the cytogenetic data or by detecting additional clones not identified when only using cytogenetic data.


Subject(s)
DNA/analysis , Flow Cytometry/methods , Karyotyping/methods , Precursor Cell Lymphoblastic Leukemia-Lymphoma/diagnosis , Adolescent , B-Lymphocytes/immunology , Cell Lineage , Child , Child, Preschool , Female , Humans , Infant , Male , Ploidies , Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics , Prognosis , T-Lymphocytes/immunology
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