Publications by authors named "Sergio F Lima Junior"

Article Synopsis
  • The Brazilian Organization for Crohn's Disease and Colitis (GEDIIB) created a national registry to study factors linked to the severity of inflammatory bowel disease (IBD) among Brazilian patients.
  • The study included 1,179 patients, primarily diagnosed with ulcerative colitis (UC) or Crohn's Disease (CD), and found that many had extensive disease, with a significant portion needing biologic treatments.
  • Factors like age, disease extent, and certain complications increased the severity of IBD, particularly for those with extensive colitis or specific disease behaviors.
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  • This study examines cases of leukocytoclastic vasculitis (LCV) linked to anti-tumor necrosis factor (TNF) therapy in patients with inflammatory bowel disease (IBD), highlighting it as a rare complication.
  • Out of 2442 assessed IBD patients, five (0.6%) were identified with LCV, mainly affecting women aged around 32 who were on anti-TNF medications like adalimumab.
  • The study emphasizes the importance of recognizing unexplained skin rashes as potential signs of LCV in IBD patients on anti-TNF therapy, as treatment with oral steroids led to complete remission in all cases.
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  • Anti-TNF therapy has proven effective in treating ulcerative colitis (UC), but there's limited data on its impact on Brazilian patients; this study compares the efficacy of adalimumab (ADA) and infliximab (IFX) in achieving clinical and endoscopic remission after one year of treatment.
  • Conducted across 24 centers, the study included 393 UC patients and utilized various statistical methods to analyze treatment outcomes, finding that IFX showed better clinical remission rates compared to ADA at 26 and 52 weeks.
  • Results indicated a clinical remission rate of 82.82% at week 52, with IFX patients experiencing fewer instances of loss of response, although endoscopic remission rates did not significantly differ between the
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Background: Colorectal cancer is a common cancer worldwide, with 5-10% of cases being hereditary. Familial adenomatous polyposis syndrome (FAP) is caused by germline mutations in the APC gene or rarely in the MUTYH gene.

Patients And Methods: This work did not identify germline mutations in the MUTYH, NTHL1, POLD1 and POLE genes in 15 individuals belonging to five families with classic FAP, who had the mutation in the APC gene confirmed in a previous study.

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Article Synopsis
  • Inflammatory bowel diseases (IBD) are increasingly common chronic conditions in Brazil that significantly affect patients' health and quality of life over time.
  • A study surveyed 286 physicians, primarily gastroenterologists and colorectal surgeons, about their experiences and challenges in treating IBD in various Brazilian regions.
  • Key findings indicated difficulties in accessing medications and performing specialized procedures, with the most prescribed treatments being biological medications like infliximab and adalimumab, while discussions about therapy failures and new treatments were highlighted as priorities for healthcare conferences.
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Objective: To evaluate the prevalence of anal intraepithelial lesions and associated risk factors in women with cervical neoplasia.

Methods: The present cross-sectional study enrolled patients with intraepithelial or invasive cervical neoplasia who had been referred to the lower genital tract pathology outpatient department of the Instituto de Medicina Integral Prof. Fernando Figueira, Recife, Brazil, between December 1, 2008, and December 31, 2009; patients with HIV infections were excluded.

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Purpose: To determine the prevalence of HPV-induced lesions in the anal canal of women with cervical intraepithelial neoplasia (CIN) grade 2/3.

Methods: A cross-sectional study was carried out from December 2008 to June 2009, in Pernambuco, northeastern Brazil. Only women with grade 2/3 CIN were included, and those who could not undergo anoscopy during their first visit were excluded.

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Aim: To characterize APC gene mutations and correlate them with patient phenotypes in individuals diagnosed with familial adenomatous polyposis (FAP) in northern Brazil.

Methods: A total of 15 individuals diagnosed with FAP from 5 different families from the north of Brazil were analyzed in this study. In addition to patients with histopathological diagnosis of FAP, family members who had not developed the disease were also tested in order to identify mutations and for possible genetic counseling.

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Background: The Human Papillomavirus (HPV) predisposes 500 000 women to cervical cancer. Host genetic background may facilitate virus persistence in the uterine cervix. Polymorphisms in regulatory and coding regions of cytokine genes have been associated with susceptibility to some human diseases.

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Chlamydia trachomatis (CT) is the most common bacterial cause of sexually transmitted disease. High-risk human papillomavirus (HR-HPV) is considered the main etiological agent for cervical neoplasia. Evidences showed that the presence of co-infection of CT and HR-HPV plays a central role in the etiology of cervical intraepithelial neoplasia (CIN) and cervical cancer.

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