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  • Original Article

    Clinical, histopathological and immunohistochemical analysis of vulvar squamous cell carcinoma

    Revista Brasileira de Ginecologia e Obstetrícia. 12-04-2024;46:e-rbgo91

    Summary

    Original Article

    Clinical, histopathological and immunohistochemical analysis of vulvar squamous cell carcinoma

    Revista Brasileira de Ginecologia e Obstetrícia. 12-04-2024;46:e-rbgo91

    DOI 10.61622/rbgo/2024rbgo91

    Views67

    Abstract

    Objective:

    The average age of patients with vulvar squamous cell carcinoma (SCC) has been reported to have declined. Human papilloma virus (HPV)-related lesions have been shown to be associated with the expression of the immunohistochemical (IHC) marker p16. Non-HPV-related tumors have been characterized by p53 abnormal expression and PDL1 expression. We aimed to evaluate the correlation between these markers and vulvar SCC and to relate it to the clinical and pathological characteristics.

    Methods:

    Histopathologic assessments and IHC analyses of p16, p53, and PDL1 were performed in 41 samples of vulvar SCC collected between 2016 and 2021. The data were correlated with clinical and pathological characteristics of the patients.

    Results:

    The mean age of the patients was 72.1 years. Positive p16 and PDL1 staining was detected in 24.4% and 17.1% of the samples, respectively. p53 expression was negative in 19.5% of the samples, whereas it was overexpressed in 24.4%. p16-positive tumors showed a smaller depth of invasion (DOI) (p = 0.014), while tumors with p53 abnormal expression showed greater DOI (p = 0.041). PDL1 expression was correlated with increased number of inflammatory cells (p = 0.055). In addition, lesions with lymphovascular space invasion were p16-negative.

    Conclusion:

    In our sample, regarding to the SCC incidence the patients’ mean age did not change. The expression of p16 was inversely correlated with p53 results. Tumors with p53 abnormal expression and absence of p16 showed a greater DOI. Our data suggest an association between PDL1 expression and increased inflammatory infiltrates in vulvar SCC.

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  • Original Article

    Low-Risk Antenatal Care Enhanced by Telemedicine: A Practical Guideline Model

    Revista Brasileira de Ginecologia e Obstetrícia. 07-19-2022;44(9):845-853

    Summary

    Original Article

    Low-Risk Antenatal Care Enhanced by Telemedicine: A Practical Guideline Model

    Revista Brasileira de Ginecologia e Obstetrícia. 07-19-2022;44(9):845-853

    DOI 10.1055/s-0042-1753505

    Views53

    Abstract

    Objective

    To develop a protocol for hybrid low-risk prenatal care adapted to Brazilian guidelines, merging reduced face-to-face consultations and remote monitoring.

    Methods

    The PubMed, Embase, and Cochrane Library databases were systematically searched on telemedicine and antenatal care perspectives and adaptation of the low-risk prenatal care protocols recommended by the Ministry of Health and by the Brazilian Federation of Gynecology and Obstetrics Associations.

    Results

    Five relevant articles and three manuals were included in the review, for presented criteria to develop this clinical guideline. We identified, in these studies, that the schedule of consultations is unevenly distributed among the gestational trimesters, and ranges from 7 to 14 appointments. In general, the authors propose one to two appointments in the first trimester, two to three appointments in the second trimester, and two to six appointments in the third trimester. Only three studies included puerperal evaluations. The routine exams recommended show minimal variations among authors. To date, there are no validated Brazilian protocols for prenatal care by telemedicine. The included studies showed that pregnant women were satisfied with this form of care, and the outcomes of interest, except for hypertensive diseases, were similar between the groups exposed to traditional and hybrid prenatal care.

    Conclusion

    The presented guideline comprises the Ministry of Health recommendations for low-risk prenatal care and reduces exposure to the hospital environment and care costs. A randomized clinical trial, to be developed by this group, will provide real-world data on safety, effectiveness, satisfaction, and costs.

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