Ectasia vascular do antro gástrico (estômago em melancia) ­ um relato de caso / Gastric antral vascular ectasia (watermelon stomach) ­ a case report

A Ectasia Vascular do Antro Gástrico (EVAG) é uma condição rara associada à hemorragia digestiva e anemia significativa. Acomete principalmente idosos e mulheres. É considerada uma anormalidade adquirida, resultando em ectasia da mucosa e da microvasculatura gástrica e é identificada na endoscopia digestiva alta (EDA). O diagnóstico pode se tornar complexo, pois a sua aparência endoscópica assemelha-se à gastropatia portal hipertensiva (GPH) ou à gastrite antral¹ , ². Este estudo tem como objetivo relatar um caso de EVAG e notificar a importância do conhecimento desta patologia, bem como a inclusão no diagnóstico diferencial à doenças como GPH e gastrite antral, para conduzir ao tratamento apropriado, pois apresenta bom prognóstico. Trata-se de um estudo descritivo, no qual foi relatado caso de paciente masculino, 76 anos, que procurou atendimento médico por acentuada anemia e melena. O paciente apresentava quadro anêmico há 6 meses, associado à fadiga, palidez e histórico de múltiplas transfusões sanguíneas. Foi requisitado EDA, o qual apresentou colunas vermelhas longitudinais no antro gástrico, possibilitando a associação com a clínica e seu diagnóstico. O paciente foi conduzido para terapêutica com o Coagulador de Plasma de Argônio e apresentou boa evolução4 . Pacientes idosos que apresentam anemia crônica sem causa aparente e/ou hemorragia digestiva alta, associada com a sintomatologia citada, devem ser endoscopicamente investigados para EVAG³. O diagnóstico desta patologia é muitas vezes dificultado, já que existem outras causas mais comuns de hemorragia digestiva, que mascaram o diagnóstico. Desta forma, destaca-se a importância do conhecimento dessa enfermidade, pois o tratamento adequado apresenta-se eficaz.

Gastric Antral Vascular Ectasia (GAVE) is a rare condition associated with digestive hemorrhage and significant anemia. It mainly affects elderly and women. It is considered an acquired abnormality, resulting in mucosal ectasia and gastric microvasculature and is identified in upper digestive endoscopy (EDA). The diagnosis can become complex, since its endoscopic appearance resembles hypertensive portal gastropathy (GPH) or antral gastritis¹, ². This study aims to report a case of GAVE and to notify the importance of the knowledge of this pathology, as well as the inclusion in the differential diagnosis to diseases such as GPH and antral gastritis, to lead to appropriate treatment, since it presents a good prognosis. This is a descriptive study, in which a case of a 76-year-old male patient who sought medical care for marked anemia and mane was reported. The patient presented an anemic condition for 6 months, associated with fatigue, pallor and history of multiple blood transfusions. EDA was requested, which presented longitudinal red columns in the gastric antrum, making possible the association with the clinic and its diagnosis. The patient was submitted to therapy with the Argon Plasma Coagulator and showed good evolution4. Elderly patients presenting with unexplained chronic anemia and / or upper gastrointestinal bleeding, associated with the mentioned symptomatology, should be endoscopically investigated for GAVE³. The diagnosis of this pathology is often difficult, since there are other more common causes of digestive hemorrhage, which mask the diagnosis. In this way, the importance of the knowledge of this disease is highlighted, since the appropriate treatment is effective.

Estrongiloidíase gástrica em paciente imunocompetente - relato de caso / Gastric strongyloidiasis in immunocompetent patients - case report

A estrongiloidíase humana é um tipo de helmintose causada por duas espécies de nematoides intestinais pertencentes ao gênero Strongyloides. O acometimento do estômago é raro, especialmente em imunocompetentes, e quando acontece os principais sintomas gastrointestinais incluem diarreia, desconforto abdominal, náusea e anorexia. O exame anatomopatológico a partir de biópsias fornece o diagnóstico definitivo. O objetivo deste trabalho é relatar um caso atípico de estrongiloidíase gástrica em paciente imunocompetente que apresentava quadro de dor abdominal difusa recorrente.

Human strongyloidiasis is a type of helminth caused by two species of intestinal nematodes belonging to the genus Strongyloides. Stomach upset is rare, especially in immunocompetent patients, and when major gastrointestinal symptoms do occur they include diarrhea, abdominal discomfort, nausea, and anorexia. Anatomopathological examination from biopsies provides the definitive diagnosis. The objective of this study was to report an atypical case of gastric strongyloidiasis in an immunocompetent patient with recurrent diffuse abdominal pain.

Clinical and laboratorial features of spontaneous bacterial peritonitis in southern Brazil / Características clínicas e laboratoriais da peritonite bacteriana espontânea no sul do Brasil

CONTEXT AND OBJECTIVE: Spontaneous bacterial peritonitis (SBP) is a severe complication that occurs in 8-27% of hospitalized patients with liver cirrhosis and ascites, with high mortality rates. This study aimed to identify the clinical characteristics associated with SBP. DESIGN AND SETTING: Cross-sectional study, conducted in a public university. METHODS: The study consecutively included individuals with liver cirrhosis and ascites between September 2009 and March 2012. Forty-five patients were included: mean age 53.2 ± 12.3 years, 82.2% male, 73.8% Caucasian, mean Model of End-stage Liver Disease (MELD) score of 19.5 ± 7.2, and 33.3% with SBP. The subjects were divided into two groups: SBP and controls. RESULTS: Comparison between individuals with SBP and controls showed that those with SBP had lower mean prothrombin activity time (36.1 ± 16.0% versus 47.1 ± 17.2%; P = 0.044) and lower median serum-ascites albumin gradient (SAAG) (1.2 versus 1.7, P = 0.045). There was a tendency towards higher mean MELD in the SBP group, not significant (22.2 ± 7.6 versus 17.9 ± 6.7; P = 0.067). There was a strong positive correlation between the neutrophil count in ascitic fluid and serum leukocyte count (r = 0.501; P = 0.001) and a negative correlation between the neutrophil count in ascitic fluid with prothrombin activity time (r = -0.385; P = 0.011). CONCLUSION: A few characteristics are associated with the presence of SBP, especially liver dysfunction, SAAG and peripheral leukocytosis. .

CONTEXTO E OBJETIVO: Peritonite bacteriana espontânea (PBE) é uma complicação grave que ocorre em 8-27% dos pacientes hospitalizados com cirrose hepática e ascite, e apresenta altas taxas de mortalidade. O objetivo deste estudo é identificar as características clínicas associadas à PBE. TIPO DE ESTUDO E LOCAL: Estudo transversal, conduzido em uma universidade pública. MÉTODOS: O estudo incluiu, consecutivamente, indivíduos com cirrose hepática e ascite entre setembro 2009 e março 2012. Foram incluídos 45 indivíduos com média de idade de 53,2 ± 12,3 anos, sendo 82,2% homens, 73,8% brancos, com MELD (Modelo para Doença Hepática Terminal) de 19,5 ± 7,2, e 33,3% com PBE. Os indivíduos foram divididos em dois grupos: PBE e controles. RESULTADOS: Quando se compararam os indivíduos com PBE aos controles, observou-se menor média de tempo de atividade da protrombina (TAP; 36,1 ± 16,0% versus 47,1 ± 17,2%; P = 0,044) e menor mediana de gradiente albumina soro-ascite (GASA; 1,2 versus 1,7; P = 0,045). Houve tendência do grupo com PBE de apresentar maior média de MELD, sem significância estatística (22,2 ± 7,6 versus 17,9 ± 6,7; P = 0,067). Foi observada forte correlação positiva entre neutrófilos do líquido ascítico e contagem sérica de leucócitos (r = 0,501; P = 0,001) e correlação negativa de neutrófilos do líquido ascítico com TAP (r = -0,385; P = 0,011). CONCLUSÃO: Poucas características estão associadas à presença de PBE, em especial a disfunção hepática, o GASA e a leucocitose periférica. .

Prevalence and clinical features of celiac disease in patients with hepatitis B virus infection in Southern Brazil

Introduction Celiac disease is an autoimmune disorder that involves gluten intolerance and can be triggered by environmental factors including hepatitis B virus (HBV) infection. This study aimed to describe the prevalence of celiac disease in individuals with HBV infection and to describe the clinical and laboratory characteristics of celiac disease associated with HBV. Methods This cross-sectional study included 50 hepatitis B patients tested for IgA anti-endomysial antibodies (EMAs) and tissue anti-transglutaminase (TTG) between August 2011 and September 2012. Results Fifty patients were included with a mean age of 46.0 ± 12.6 (46.0) years; 46% were female and 13% were HBeAg+. Six patients had positive serology for celiac disease, four were EMA+, and five were TTG+. When individuals with positive serology for celiac disease were compared to those with negative serology, they demonstrated a higher prevalence of abdominal pain (100% vs. 33.3%, p = 0.008), lower median creatinine (0.7mg/dL vs. 0.9mg/dL, p = 0.007) and lower mean albumin (3.6 ± 0.4g/L vs. 3.9 ± 0.3g/L, p = 0.022). All individuals with positive serology for celiac disease underwent upper digestive endoscopy, and three of the patients exhibited a macroscopic pattern suggestive of celiac disease. Histologically, five patients demonstrated an intra-epithelial lymphocytic infiltrate level > 30%, and four patients showed villous atrophy associated with crypt hyperplasia on duodenal biopsy. Conclusions An increased prevalence of celiac disease was observed among hepatitis B patients. These patients were symptomatic and had significant laboratory abnormalities. These results indicate that active screening for celiac disease among HBV-infected adults is warranted. .

Autoantibody profile in individuals with chronic hepatitis C

Introduction Autoantibodies are often produced during infection with chronic hepatitis C virus (HCV), but it remains controversial whether they influence the biochemical profile and histological features of this disease. Therefore, this current study sought to describe these autoantibodies and evaluate their impact on the clinical and histological presentation of hepatitis C. Methods This cross-sectional analytical study assessed patients with HCV (RNA+) from October 2011 to July 2012. Results This study included 66 patients, with a mean age of 53.2±10.5 years. Of these patients, 60.6% were male, and 54.3% presented with genotype 1. Non-organ-specific autoantibodies (NOSA) were detected in 24% of the patients; of these, 7.6% were anti-mitochondrial antibodies (AMA+), 26.7% were anti-smooth muscle antibodies (SMA+) and 6.8% were liver kidney microsomal type 1 antibodies (LKM1+). With respect to the thyroid autoantibodies, 7.4% were anti-peroxidase (ATPO+) antibodies, and none were anti-thyroglobulin (ATG+) antibodies. Regarding celiac disease autoantibodies, 5.8% were endomysial antibodies (EMA+), and no transglutaminase (TTG+) antibodies were detected. Cryoglobulins were found in 2.1% of patients. When NOSA+ individuals were compared to patients without the presence of NOSAs, they exhibited higher median alkaline phosphatase (0.7 vs. 0.6 xULN; p=0.041), lower median platelet counts (141,500.0 vs. 180,500.0/mm 3 ; p=0.036), lower mean prothrombin activity (72.6±11.5% vs. 82.2±16.0%; p=0.012) and an increased prevalence of significant fibrosis (E≥2) (45.5% vs. 18.2%; p=0.012). There was also a tendency for a greater proportion of NOSA+ cases to have marked periportal activity (APP≥3) (44.5% vs. 15.6%; p=0.087). Conclusions In addition to the high prevalence of autoantibodies associated with HCV infection, it was observed that NOSA ...