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1.
Pancreas ; 50(6): 815-821, 2021 07 01.
Article in English | MEDLINE | ID: mdl-34347723

ABSTRACT

OBJECTIVES: Rapid on-site evaluation (ROSE) by cytopathologists during endoscopic ultrasound-fine-needle aspiration (EUS-FNA) of solid pancreatic lesions (SPLs) improves adequacy and diagnostic accuracy while reducing the number of needle passes. We evaluated the usefulness of ROSE performed by the endosonographer. METHODS: Patients with an SPL were randomly assigned to EUS-FNA with ROSE or non-ROSE. Procedure duration, number of needle passes, specimen adequacy, and adverse event rates were compared. RESULTS: Sixty-five patients were enrolled (33 in the ROSE vs 32 in the non-ROSE group). Both groups were similar in terms of age, sex, size, and location of the lesion. Specimen adequacy rates were high and similar between groups. Mean (standard deviation) procedure duration was shorter in the ROSE versus non-ROSE group (30.0 [11.3] vs 37.0 [7.2] minutes, P < 0.005), as well as the mean (standard deviation) number of needle passes (2.6 [0.8] vs 3.5 [0.8], P < 0.005). Accuracy parameters as sensitivity and accuracy of ROSE by the endosonographer for malignancy were 93% and 88%, respectively. CONCLUSIONS: After specific training, the endosonographer can accurately evaluate samples during EUS-FNA of SPL, allowing for a shorter procedure duration and a lower number of needle passes.


Subject(s)
Endoscopic Ultrasound-Guided Fine Needle Aspiration/methods , Endosonography/methods , Pancreas/diagnostic imaging , Pancreatic Neoplasms/diagnostic imaging , Rapid On-site Evaluation , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Pancreas/pathology , Pancreatic Neoplasms/pathology , Prospective Studies , Reproducibility of Results , Sensitivity and Specificity , Young Adult
2.
J Med Virol ; 90(3): 599-603, 2018 03.
Article in English | MEDLINE | ID: mdl-29064575

ABSTRACT

To identify decoy cells, cytological examination was performed in urine cytospin slides. Decoy cells are related to Polyomaviruses (JC virus [JCV] and BK virus [BKV]), which are recognized worldwide due to potential infection and morbidity in kidney transplant recipients. Cytologically, it is difficult to evaluate the cytopathic effect of JCV and BKV in urine of patients with urothelial neoplasia. For this reason, there is a need for molecular approaches. To evaluate the incidence of BKV and JCV DNA in archival slides of urine cytospin material with benign and malignant characteristics. A total of 176 urine specimens were used for cytological examination of neoplastic or decoy cells. The samples were analyzed for the presence of JCV and BKV, by polymerase chain reaction (PCR) in DNA Isolated from archival slides of urine cytospin material. A typical samples (n = 48) were compared with the remaining 128 samples without atypia/neoplasia for the presence of JCV or BKV DNA. A statistically nonsignificant result was observed correlating the presence of JCV or BKV. The results show that DNA Isolated from archival slides of urine cytospin material can be used for detection of BKV and JCV.


Subject(s)
BK Virus/isolation & purification , Biological Specimen Banks , Cytological Techniques/instrumentation , DNA, Viral/urine , JC Virus/isolation & purification , Urothelium/virology , BK Virus/genetics , Cytological Techniques/methods , DNA, Viral/isolation & purification , Genome, Viral , Humans , Incidence , JC Virus/genetics , Kidney Transplantation , Neoplasms/virology , Polymerase Chain Reaction , Polyomavirus Infections/diagnosis , Tumor Virus Infections/diagnosis , Urothelium/pathology
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