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1.
J Pediatr ; 127(1): 137-46, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7608800

ABSTRACT

OBJECTIVES: Human immunodeficiency virus (HIV) infection in children can be complicated by the development of cardiac disease. Decreased left ventricular function has been temporally associated with the use of zidovudine (azidothymidine; AZT) in adults with HIV and has been associated with changes in cardiac muscle mitochondria in animal models. This study was done in an attempt to determine whether the cardiac disease is related to the antiretroviral therapy or to progressive HIV infection. METHODS: We retrospectively reviewed echocardiograms, clinical records, and laboratory data from 137 HIV-infected children who were being treated by the Pediatric Branch, National Cancer Institute, and who were receiving AZT or didanosine, both drugs, or no antiretroviral therapy. RESULTS: Despite correction of the echocardiographic results for HIV disease severity with markers such as CD4+ lymphocyte count, time since infection, mode of acquisition of HIV, and age, children who were treated with AZT had a lower average fractional shortening than those who were not treated with AZT (p < 0.00001). There was a nonlinear relation between days of AZT use and this There was a nonlinear relation between days of AZT use and this decrease in fractional shortening. The odds that a cardiomyopathy would develop was 8.4 times greater in children who had previously used AZT than in those who had never taken AZT (95% confidence interval, 1.7 to 42.0). Didanosine was not associated with the development of a cardiomyopathy. CONCLUSIONS: Treatment of HIV-infected children with AZT may be associated with the development of a cardiomyopathy; didanosine does not appear to increase the risk of cardiomyopathy. The continued use of AZT in a child in whom a cardiomyopathy develops should be carefully assessed, and all children receiving AZT should be followed by serial cardiac examination and echocardiograms.


Subject(s)
Acquired Immunodeficiency Syndrome/drug therapy , Didanosine/pharmacology , Didanosine/therapeutic use , HIV , Heart/drug effects , Zalcitabine/pharmacology , Zalcitabine/therapeutic use , Zidovudine/pharmacology , Zidovudine/therapeutic use , CD4 Lymphocyte Count , Cardiomyopathies/diagnosis , Cardiomyopathies/etiology , Cardiomyopathies/physiopathology , Child, Preschool , Dose-Response Relationship, Drug , Echocardiography , Female , Heart/physiopathology , Humans , Infant , Infant, Newborn , Male , Medical Records , Retrospective Studies , Severity of Illness Index , Zidovudine/adverse effects
2.
Am J Surg Pathol ; 19(3): 357-63, 1995 Mar.
Article in English | MEDLINE | ID: mdl-7872434

ABSTRACT

A malignant lymphoma arising in the lung of a pediatric HIV-positive patient exhibited histologic and clinical features of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue (MALT). Clinically, the neoplasm consisted of a 4-cm mass in the left-upper lobe of the lung of a 7-year-old girl. The lung mass was surgically resected. Monoclonal immunoglobulin heavy and light chain gene rearrangements were shown by Southern blot. Monoclonality of light chain expression was demonstrated by immunohistochemistry. Coexpression of Leu-22 (CD43) by the tumor cells supported the diagnosis of lymphoma. The remainder of the pulmonary parenchyma distal to the mass was associated with pulmonary lymphoid hyperplasia/lymphocytic interstitial pneumonitis, which may have been a predisposing factor. Gastric MALT lymphomas have recently been described in adult HIV-antibody-positive patients. Ours represents the first reported case of a pulmonary MALT lymphoma in a pediatric HIV-positive patient. In addition, at age 7, this is the youngest patient reported with a MALT lymphoma.


Subject(s)
HIV Seropositivity/complications , Lung Neoplasms/complications , Lymphoma, B-Cell, Marginal Zone/complications , Child , Female , Gene Rearrangement , HIV Seropositivity/pathology , Humans , Immunohistochemistry , Lung Neoplasms/chemistry , Lung Neoplasms/genetics , Lung Neoplasms/pathology , Lymphoma, B-Cell, Marginal Zone/chemistry , Lymphoma, B-Cell, Marginal Zone/genetics , Lymphoma, B-Cell, Marginal Zone/pathology
3.
Pediatr Res ; 37(1): 70-4, 1995 Jan.
Article in English | MEDLINE | ID: mdl-7700736

ABSTRACT

Among coagulase-negative staphylococci, Staphylococcus epidermidis is the species most commonly implicated in catheter-related infections. Whether some staphylococcal organisms are inherently more virulent than others, or whether their ability to infect relates more to the sheer numbers of organisms at the catheter site, remains unclear. We therefore compared eight S. epidermidis isolates and two other coagulase-negative staphylococci using a murine model that allowed us to quantify catheter colonization and abscess formation in the same animal. The organisms were isolated from different clinically relevant settings and were classified according to their slime phenotype. The ability to evoke abscesses or colonize catheters in half of the animals (ID50) was assessed. ID50 inoculum titers (log10 data +/- SD) ranged widely, from 8.5 +/- 0.3 to 10.2 +/- 0.2 for abscess formation (p < 0.005) and from 7.5 +/- 0.5 to 10.3 +/- 1.0 for catheter colonization (p < 0.005). ID50 values by statistical criteria suggested variability among organisms in the ability to induce abscess formation. High slime production correlated with both parameters, but not with the clinical source of the isolate. Our findings demonstrate impressive heterogeneity in the ability of a representative group of S. epidermidis isolates to colonize catheters and to evoke abscess formation and implicate slime productivity as a major virulence factor. The murine model used permitted simultaneous analysis of multiple factors involved in pathogenesis and should be useful in establishing the basis of S. epidermidis pathogenicity.


Subject(s)
Catheterization, Central Venous/adverse effects , Staphylococcal Infections/etiology , Staphylococcus epidermidis/pathogenicity , Abscess/etiology , Abscess/microbiology , Animals , Colony Count, Microbial , Disease Models, Animal , Humans , Mice , Phenotype , Staphylococcal Infections/microbiology , Staphylococcus epidermidis/isolation & purification , Virulence
4.
Clin Infect Dis ; 17(3): 484-90, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8218694

ABSTRACT

We identified 24 children treated for malignancies between 1962 and 1992 who had antemortem diagnoses of typhlitis that were confirmed on review. The study criteria specified the presence of fever, abdominal pain, and tenderness, with radiological evidence of right-sided colonic inflammation. Typhlitis was most frequent in patients treated for acute leukemias. Computed tomography and ultrasonography were more sensitive than plain radiography (false-negative rates, 15%, 23%, and 48%, respectively). The wider availability of these sensitive procedures and the increased intensity of chemotherapeutic regimens may account for a marked increase in the incidence of typhlitis over the past 5 years. Most patients responded to aggressive medical management, and typhlitis was fatal in only two cases (1 of 21 cases managed medically and 1 of 3 taken to surgery). Seven patients are alive > 1 year following the diagnosis. These findings contrast with prior descriptions of typhlitis as a preterminal event. Computed tomography and/or ultrasonography should be performed in all neutropenic patients with right-lower-quadrant signs to permit prompt diagnosis and treatment.


Subject(s)
Cecal Diseases/drug therapy , Colitis/drug therapy , Neoplasms/complications , Adolescent , Adult , Anti-Bacterial Agents/therapeutic use , Cecal Diseases/diagnosis , Cecal Diseases/etiology , Child , Child, Preschool , Colitis/diagnosis , Colitis/etiology , Female , Humans , Male
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