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2.
Int J STD AIDS ; 32(6): 582-584, 2021 05.
Article in English | MEDLINE | ID: mdl-33533293

ABSTRACT

Kaposi sarcoma (KS) is an angioproliferative disease that is caused by human herpesvirus 8. The epidemic form of KS is associated with acquired immunodeficiency syndrome (AIDS) and is common in HIV-positive patients with CD4 counts less than 200 cells/mm. We present the case of a 63-year-old man with well-controlled HIV and normal CD4 count developing atypical nasal KS associated with intranasal steroid use.


Subject(s)
Acquired Immunodeficiency Syndrome , Herpesvirus 8, Human , Sarcoma, Kaposi , CD4 Lymphocyte Count , Humans , Male , Middle Aged , Steroids/adverse effects
3.
J Mol Diagn ; 9(3): 394-400, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17591939

ABSTRACT

The potential presence of maternal cell contamination (MCC) in chorionic villus or amniotic fluid samples poses a serious preanalytical risk for prenatal misdiagnosis. The aim of this study was to identify current diagnostic practices in the absence of comprehensive practice guidelines. Thirty-five clinical molecular laboratories that conduct prenatal testing agreed to participate in a clinical practice survey. The survey included questions about sample requirements, test indications, assay type, test performance and limitations, criteria and management of uninformative test results, reporting, and billing. Sixty percent of participating laboratories performed testing on direct and cultured amniotic fluid, whereas forty percent tested cultured cells only. Most also accepted chorionic villus samples. Although MCC testing of fetal samples is recommended in guidelines by the American College of Medical Genetics, only 60% of surveyed laboratories performed it without exception. Commercially available assays were used by 75% of participating laboratories, and at least five identity markers were evaluated at 87% of the laboratories. The reported lower limit of MCC detection ranged from 1 to 20% but was not determined in all laboratories. MCC testing was performed in the majority of molecular diagnostic laboratories, but guidelines for standardization are needed to ensure optimal and accurate prenatal patient care.


Subject(s)
Artifacts , Clinical Laboratory Techniques , Diagnostic Errors/prevention & control , Maternal-Fetal Exchange , Prenatal Diagnosis/methods , Specimen Handling/methods , Algorithms , Cells, Cultured , Clinical Laboratory Techniques/economics , Clinical Laboratory Techniques/standards , Data Collection , Data Interpretation, Statistical , Female , Humans , Molecular Diagnostic Techniques/standards , Practice Patterns, Physicians'/economics , Practice Patterns, Physicians'/standards , Pregnancy , Prenatal Diagnosis/economics , Prenatal Diagnosis/standards , Sensitivity and Specificity , Specimen Handling/standards , Surveys and Questionnaires
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