RESUMEN

Behçet's disease is a multisystemic disease consisting of a varying combination of ocular, mucocutaneous, neurologic, cardiovascular, gastrointestinal and other manifestations. Its diagnosis is based on clinical criteria, in which a positive pathergy test scores 1. A case series with 26 suspected patients is presented, and the skin pathergy test was performed in 23. The results were read in 48hours, and they were considered negative when without papule, and positive with a papule or pustule. Positive results were divided by papule size, and dermatoscopy was done to measure and observe its clinical aspects. After the readings, a biopsy was performed, with annotation of histopathological aspects. The test was negative in 2 (8.7%) and positive in 21 (91.3%) patients. The results and the literature review are presented.

Asunto(s)

Síndrome de Behçet/diagnóstico por imagen , Dermoscopía , Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pruebas Cutáneas/métodos , Adulto Joven

RESUMEN

OBJECTIVE: Iron deficiency (ID) and iron deficiency anaemia (IDA) are global major public health problems, particularly in developing countries. Whilst an association between H. pylori infection and ID/IDA has been proposed in the literature, currently there is no consensus. We studied the effects of H. pylori infection on ID/IDA in a cohort of children undergoing upper gastrointestinal endoscopy for upper abdominal pain in two developing and one developed country. METHODS: In total 311 children (mean age 10.7±3.2 years) from Latin America--Belo Horizonte/Brazil (n = 125), Santiago/Chile (n = 105)--and London/UK (n = 81), were studied. Gastric and duodenal biopsies were obtained for evaluation of histology and H. pylori status and blood samples for parameters of ID/IDA. RESULTS: The prevalence of H. pylori infection was 27.7% being significantly higher (p<0.001) in Latin America (35%) than in UK (7%). Multiple linear regression models revealed H. pylori infection as a significant predictor of low ferritin and haemoglobin concentrations in children from Latin-America. A negative correlation was observed between MCV (r = -0.26; p = 0.01) and MCH (r = -0.27; p = 0.01) values and the degree of antral chronic inflammation, and between MCH and the degree of corpus chronic (r = -0.29, p = 0.008) and active (r = -0.27, p = 0.002) inflammation. CONCLUSIONS: This study demonstrates that H. pylori infection in children influences the serum ferritin and haemoglobin concentrations, markers of early depletion of iron stores and anaemia respectively.

Asunto(s)

Dolor Abdominal/sangre , Anemia Ferropénica/sangre , Ferritinas/metabolismo , Infecciones por Helicobacter/sangre , Hemoglobinas/metabolismo , Hierro/sangre , Dolor Abdominal/complicaciones , Dolor Abdominal/microbiología , Dolor Abdominal/patología , Adolescente , Anemia Ferropénica/complicaciones , Anemia Ferropénica/microbiología , Anemia Ferropénica/patología , Biopsia , Brasil/epidemiología , Niño , Chile/epidemiología , Duodenoscopía , Duodeno/metabolismo , Duodeno/microbiología , Duodeno/patología , Femenino , Mucosa Gástrica/metabolismo , Gastroscopía , Infecciones por Helicobacter/complicaciones , Infecciones por Helicobacter/microbiología , Infecciones por Helicobacter/patología , Helicobacter pylori/aislamiento & purificación , Helicobacter pylori/metabolismo , Humanos , Londres/epidemiología , Masculino , Prevalencia , Estómago/microbiología , Estómago/patología

RESUMEN

AIM: To evaluate and compare detection of lymphatic and blood vessel invasion (LVI and BVI) by hematoxylin-eosin (HE) and immunohistochemistry (IHC) in gastric cancer specimens, and to correlate with lymph node status. METHODS: IHC using D2-40 (a lymphatic endothelial marker) and CD34 (a pan-endothelial marker) was performed to study LVI and BVI in surgical specimens from a consecutive series of 95 primary gastric cancer cases. The results of the IHC study were compared with the detection by HE using McNemar test and kappa index. The morphologic features of the tumors and the presence of LVI and BVI were related to the presence of lymph node metastasis. A χ(2) test was performed to obtain associations between LVI and BVI and other prognostic factors for gastric cancer. RESULTS: The detection rate of LVI was considerably higher than that of BVI. The IHC study identified eight false-positive cases and 13 false-negative cases for LVI, and 24 false-positive cases and 10 false-negative cases for BVI. The average Kappa value determined was moderate for LVI (κ = 0.50) and low for BVI (κ = 0.20). Both LVI and BVI were statistically associated with the presence of lymph node metastasis (HE: P = 0.001, P = 0.013, and IHC: P = 0.001, P = 0.019). The morphologic features associated with LVI were location of the tumor in the distal third of the stomach (P = 0.039), Borrmann's macroscopic type (P = 0.001), organ invasion (P = 0.03) and the depth of tumor invasion (P = 0.001). The presence of BVI was related only to the depth of tumor invasion (P = 0.003). CONCLUSION: The immunohistochemical identification of lymphatic and blood vessels is useful for increasing the accuracy of the diagnosis of vessel invasion and for predicting lymph node metastasis.

Asunto(s)

Técnicas de Preparación Histocitológica/métodos , Ganglios Linfáticos/patología , Neovascularización Patológica/diagnóstico , Neovascularización Patológica/patología , Neoplasias Gástricas/diagnóstico , Neoplasias Gástricas/patología , Anticuerpos Monoclonales de Origen Murino/metabolismo , Antígenos CD34/metabolismo , Biomarcadores de Tumor/metabolismo , Reacciones Falso Negativas , Reacciones Falso Positivas , Femenino , Humanos , Ganglios Linfáticos/metabolismo , Metástasis Linfática , Masculino , Neovascularización Patológica/metabolismo , Pronóstico , Neoplasias Gástricas/metabolismo

RESUMEN

Association between H. pylori infection, iron deficiency and iron deficiency anaemia has been described, but the mechanisms involved have not been established. We hypothesized that in H. pylori infected children increased gastric concentrations of IL-1ß and/or TNF-α, both potent inhibitors of gastric acid secretion that is essential for iron absorption, are predictors for low blood concentrations of ferritin and haemoglobin, markers of early depletion of iron stores and anaemia, respectively. We evaluated 125 children undergoing endoscopy to clarify the origin of gastrointestinal symptoms. Gastric specimens were obtained for H. pylori status and cytokine evaluation and blood samples for determination of iron deficiency/iron deficiency anaemia parameters and IL1 cluster and TNFA polymorphisms that are associated with increased cytokine secretions. Higher IL-1ß and TNF-α gastric concentrations were observed in H. pylori-positive (n = 47) than in -negative (n = 78) children. Multiple linear regression models revealed gastric IL-1ß, but not TNF-α, as a significant predictor of low ferritin and haemoglobin concentrations; results were reproduced in young children in whom IL1RN polymorphic genotypes associated with higher gastric IL-1ß expression and lower blood ferritin and haemoglobin concentrations. In conclusion, high gastric levels of IL-1ß can be the link between H. pylori infection and iron deficiency/iron deficiency anaemia in childhood.

Asunto(s)

Anemia Ferropénica/microbiología , Mucosa Gástrica/metabolismo , Infecciones por Helicobacter/metabolismo , Helicobacter pylori/aislamiento & purificación , Interleucina-1beta/metabolismo , Hierro/metabolismo , Estómago/microbiología , Adolescente , Anemia Ferropénica/genética , Anemia Ferropénica/metabolismo , Niño , Preescolar , Endoscopía/métodos , Femenino , Ferritinas/genética , Ferritinas/metabolismo , Genotipo , Infecciones por Helicobacter/sangre , Infecciones por Helicobacter/genética , Infecciones por Helicobacter/microbiología , Humanos , Proteína Antagonista del Receptor de Interleucina 1/genética , Proteína Antagonista del Receptor de Interleucina 1/metabolismo , Interleucina-1beta/genética , Hierro/sangre , Masculino , Polimorfismo Genético , Factor de Necrosis Tumoral alfa/genética , Factor de Necrosis Tumoral alfa/metabolismo

RESUMEN

OBJECTIVE: Burkitt's lymphoma is the most common subtype of non-Hodgkin lymphoma in children. The aim of this study was to characterize the clinical course and prognostic factors of children and adolescents with Burkitt's lymphoma treated in the Hematology Unit of Hospital das Clínicas, Universidade Federal de Minas Gerais (UFMG). METHODS: A retrospective cohort study was made of 50 consecutive cases of children and adolescents aged 16 years or less with Burkitt's lymphoma admitted between January 1981 and December 2007. Prognostic factors associated with death were evaluated using the Kaplan-Meier method and compared by the two-tailed log-rank test. RESULTS: The median age at diagnosis was 4.7 years. Most patients had abdominal tumors (66.7%) and advanced disease (68.9%) at diagnosis. Thirty-eight patients (84.4%) achieved complete clinical remission and 33 (73.3%) were alive at the first remission. Twelve children (26.7%) died. The median follow-up was 35 months with the probability of overall survival being 73% (89.2% and 35.7% for patients with uric acid < 7 mg/dL and ≥ 7.0 mg/dL, respectively - p-value < 0.001). Uric acid was the only significant prognostic factor at diagnosis. CONCLUSION: Our findings confirm the favorable prognosis of children with Burkitt's lymphoma even when treated with intermediate doses of methotrexate (500 mg/m2). Survival was significantly lower for individuals with concentrations of uric acid > 7 mg/dL.

RESUMEN

OBJECTIVE: Burkitt's lymphoma is the most common subtype of non-Hodgkin lymphoma in children. The aim of this study was to characterize the clinical course and prognostic factors of children and adolescents with Burkitt's lymphoma treated in the Hematology Unit of Hospital das Clínicas, Universidade Federal de Minas Gerais (UFMG). METHODS: A retrospective cohort study was made of 50 consecutive cases of children and adolescents aged 16 years or less with Burkitt's lymphoma admitted between January 1981 and December 2007. Prognostic factors associated with death were evaluated using the Kaplan-Meier method and compared by the two-tailed log-rank test. RESULTS: The median age at diagnosis was 4.7 years. Most patients had abdominal tumors (66.7%) and advanced disease (68.9%) at diagnosis. Thirty-eight patients (84.4%) achieved complete clinical remission and 33 (73.3%) were alive at the first remission. Twelve children (26.7%) died. The median follow-up was 35 months with the probability of overall survival being 73% (89.2% and 35.7% for patients with uric acid < 7 mg/dL and > 7.0 mg/dL, respectively - p-value < 0.001). Uric acid was the only significant prognostic factor at diagnosis. CONCLUSION: Our findings confirm the favorable prognosis of children with Burkitt's lymphoma even when treated with intermediate doses of methotrexate (500 mg/m2). Survival was significantly lower for individuals with concentrations of uric acid > 7 mg/dL.

Asunto(s)

Humanos , Masculino , Femenino , Preescolar , Niño , Pronóstico , Sobrevida , Ácido Úrico , Linfoma no Hodgkin , Niño , Linfoma de Burkitt

RESUMEN

The hypothesis that Helicobactermight be a risk factor for human liver diseases has arisen after the detection of Helicobacter DNA in hepatic tissue of patients with hepatobiliary diseases. Nevertheless, no explanation that justifies the presence of the bacterium in the human liver has been proposed. We evaluated the presence of Helicobacterin the liver of patients with hepatic diseases of different aetiologies. We prospectively evaluated 147 patients (106 with primary hepatic diseases and 41 with hepatic metastatic tumours) and 20 liver donors as controls. Helicobacter species were investigated in the liver by culture and specific 16S rDNA nested-polymerase chain reaction followed by sequencing. Serum and hepatic levels of representative cytokines of T regulatory cell, T helper (Th)1 and Th17 cell lineages were determined using enzyme linked immunosorbent assay. The data were evaluated using logistic models. Detection of Helicobacter pylori DNA in the liver was independently associated with hepatitis B virus/hepatitis C virus, pancreatic carcinoma and a cytokine pattern characterised by high interleukin (IL)-10, low/absent interferon-γ and decreased IL-17A concentrations (p < 10(-3)). The bacterial DNA was never detected in the liver of patients with alcoholic cirrhosis and autoimmune hepatitis that are associated with Th1/Th17 polarisation. H. pylori may be observed in the liver of patients with certain hepatic and pancreatic diseases, but this might depend on the patient cytokine profile.

Asunto(s)

Citocinas/inmunología , Infecciones por Helicobacter/inmunología , Helicobacter pylori/aislamiento & purificación , Hepatopatías/microbiología , Hígado/microbiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Estudios de Casos y Controles , ADN Bacteriano/aislamiento & purificación , ADN Ribosómico/aislamiento & purificación , Ensayo de Inmunoadsorción Enzimática , Femenino , Helicobacter pylori/genética , Humanos , Inmunohistoquímica , Hepatopatías/inmunología , Masculino , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa , Estudios Prospectivos , Células TH1/inmunología , Células Th17/inmunología , Adulto Joven

RESUMEN

OBJECTIVES: To improve the level of 'definitive' diagnosis of Langerhans cell histiocytosis by immunohistochemical investigation of the CD1a surface antigen and to compare outcomes in respect to age, gender, stage of the disease, treatment response and level of diagnostic accuracy. METHODS: A retrospective study was carried out of 37 children and adolescents with possible Langerhans cell histiocytosis between 1988 and 2008. The diagnoses were revisited using immunohistochemical investigations for CD1a, S-100 and CD68 in an attempt to reach definitive diagnoses for all cases. RESULTS: Before the study, only 13 of 37 patients (35.1 percent) had a 'definitive' diagnosis; by the end of the study, this number rose to 25 patients (67.6 percent). All reviewed cases were positive for the CD1a antigen. Overall survival was 88.5 percent. Multisystem disease (Stage 2; n=19) and absence of response at the 6th week of therapy (n=5) were associated to significantly lower overall survival (p-value = 0.04 and 0.0001, respectively). All deaths occurred in patients with multisystem disease and organ dysfunction at diagnosis. Other potential prognostic factors were not significant. Reactivation episodes occurred in 75 percent of the patients with multisystem disease. Diabetes insipidus was the most common sequel (21.6 percent). CONCLUSION: The level of diagnostic accuracy was increased through immunohistochemistry. The overall survival rate was similar to international multicentric studies. Multisystem disease and absence of response at six weeks of treatment were the most important unfavorable prognostic factors. The frequency of reactivation for patients with multisystem disease was higher than described in the literature, probably because maintenance chemotherapy was used only in two cases.

Asunto(s)

Humanos , Masculino , Femenino , Niño , Adolescente , Diabetes Insípida , Histiocitosis de Células de Langerhans/patología , Otitis

RESUMEN

The hypothesis that Helicobactermight be a risk factor for human liver diseases has arisen after the detection of Helicobacter DNA in hepatic tissue of patients with hepatobiliary diseases. Nevertheless, no explanation that justifies the presence of the bacterium in the human liver has been proposed. We evaluated the presence of Helicobacterin the liver of patients with hepatic diseases of different aetiologies. We prospectively evaluated 147 patients (106 with primary hepatic diseases and 41 with hepatic metastatic tumours) and 20 liver donors as controls. Helicobacter species were investigated in the liver by culture and specific 16S rDNA nested-polymerase chain reaction followed by sequencing. Serum and hepatic levels of representative cytokines of T regulatory cell, T helper (Th)1 and Th17 cell lineages were determined using enzyme linked immunosorbent assay. The data were evaluated using logistic models. Detection of Helicobacter pylori DNA in the liver was independently associated with hepatitis B virus/hepatitis C virus, pancreatic carcinoma and a cytokine pattern characterised by high interleukin (IL)-10, low/absent interferon-γ and decreased IL-17A concentrations (p < 10-3). The bacterial DNA was never detected in the liver of patients with alcoholic cirrhosis and autoimmune hepatitis that are associated with Th1/Th17 polarisation. H. pylori may be observed in the liver of patients with certain hepatic and pancreatic diseases, but this might depend on the patient cytokine profile.

Asunto(s)

Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Citocinas/inmunología , Infecciones por Helicobacter/inmunología , Helicobacter pylori/aislamiento & purificación , Hepatopatías/microbiología , Hígado/microbiología , Estudios de Casos y Controles , ADN Bacteriano/aislamiento & purificación , ADN Ribosómico/aislamiento & purificación , Ensayo de Inmunoadsorción Enzimática , Helicobacter pylori/genética , Inmunohistoquímica , Hepatopatías/inmunología , Reacción en Cadena de la Polimerasa , Estudios Prospectivos , Células TH1/inmunología , /inmunología

RESUMEN

OBJECTIVES: To improve the level of 'definitive' diagnosis of Langerhans cell histiocytosis by immunohistochemical investigation of the CD1a surface antigen and to compare outcomes in respect to age, gender, stage of the disease, treatment response and level of diagnostic accuracy. METHODS: A retrospective study was carried out of 37 children and adolescents with possible Langerhans cell histiocytosis between 1988 and 2008. The diagnoses were revisited using immunohistochemical investigations for CD1a, S-100 and CD68 in an attempt to reach definitive diagnoses for all cases. RESULTS: Before the study, only 13 of 37 patients (35.1%) had a 'definitive' diagnosis; by the end of the study, this number rose to 25 patients (67.6%). All reviewed cases were positive for the CD1a antigen. Overall survival was 88.5%. Multisystem disease (Stage 2; n=19) and absence of response at the 6th week of therapy (n=5) were associated to significantly lower overall survival (p-value = 0.04 and 0.0001, respectively). All deaths occurred in patients with multisystem disease and organ dysfunction at diagnosis. Other potential prognostic factors were not significant. Reactivation episodes occurred in 75% of the patients with multisystem disease. Diabetes insipidus was the most common sequel (21.6%). CONCLUSION: The level of diagnostic accuracy was increased through immunohistochemistry. The overall survival rate was similar to international multicentric studies. Multisystem disease and absence of response at six weeks of treatment were the most important unfavorable prognostic factors. The frequency of reactivation for patients with multisystem disease was higher than described in the literature, probably because maintenance chemotherapy was used only in two cases.

RESUMEN

BACKGROUND: Polymorphisms in genes linked to the innate and adaptive immune response may be involved in inflammatory bowel disease pathogenesis. Our aim was to investigate associations among IL1B-511, IL1B-31, IL1RN, TNFA-307, TLR-2, TLR-4, IL2-330, NOD2 G908R, NOD2 L1007fsinsC polymorphisms and both Crohn's disease (CD) and ulcerative colitis (UC) in a Brazilian population. METHODS: We studied 43 patients with CD, 42 with UC, and 541 blood donors. Polymorphisms were evaluated by PCR, PCR-CTPP, or PCR-RFLP. Data were analyzed in multivariate models adjusting for confounding factors. RESULTS: IL1RN VNTR (P = 0.00, odds ratio [OR] = 2.43, 95% confidence interval [CI] = 1.50-3.90), as well as TNFA-307 polymorphic allele (P = 0.05, OR = 1.70, 95% CI = 1.00-2.94) were associated with UC. Both NOD2 mutations (G908R, P = 0.02, OR = 6.83, 95% CI = 1.62-25.45, and L1007fsinsC, P = 0.00, OR = 20.00, 95% CI = 3.21-124.69) were associated with CD. CONCLUSIONS: Our analyses showed positive associations between proinflammatory polymorphisms at IL1RN and TNFA-307 loci and UC, as well as polymorphisms in the NOD2 gene and CD. These results highlight the importance of different genetic profiles associated with CD and UC.

Asunto(s)

Colitis Ulcerosa/inmunología , Enfermedad de Crohn/inmunología , ADN/genética , Inmunidad Celular/inmunología , Proteína Adaptadora de Señalización NOD2/genética , Polimorfismo Genético , Adulto , Alelos , Brasil/epidemiología , Colitis Ulcerosa/epidemiología , Colitis Ulcerosa/genética , Enfermedad de Crohn/epidemiología , Enfermedad de Crohn/genética , Femenino , Estudios de Seguimiento , Genotipo , Humanos , Proteína Antagonista del Receptor de Interleucina 1/genética , Proteína Antagonista del Receptor de Interleucina 1/metabolismo , Desequilibrio de Ligamiento , Masculino , Proteína Adaptadora de Señalización NOD2/metabolismo , Reacción en Cadena de la Polimerasa , Prevalencia , Estudios Retrospectivos

RESUMEN

A esofagite eosinofílica (EE) é uma doença ainda pouco conhe»cida, cuja prevalência vem aumentando progressivamente, possi»velmente em decorrência de estar sendo mais diagnosticada. E uma condição inflamatória em que há grande infiltrado eosinofílico no epitélio esofágico. Seu quadro clínico inclui: disfagia, impactação de alimentos, dor retroestemal e náuseas/vômitos. Acomete pre»ferencialmente crianças e adultos jovens. Foi realizado estudo re-trospectivo em serviço de histopatologia em Belo Horizonte (MG), no período de janeiro de 2006 a fevereiro de 2007, visando à caracterização de aspectos histopatológicos do esôfago e à pro»posta de uma classificação, acrescido de uma revisão bibliográfica sobre o assunto. Foram identificadas 25 biópsias esofágicas endos»cópicas com contagens elevadas de eosinófilos. Dos 25 casos, 1 7 eram do sexo masculino (68%) e oito do feminino (32%). Os es»pécimes analisados apresentaram diferentes números de eosinófi»los por campo de grande aumento (eosinófilos/hpf) e foram clas»sificados em quatro diferentes graus: grau O - 0%, (N = O), até 14 eosinófilos/hpf; grau I - 48%, (N = 12), de 15 a 30 eosinófilos/ hpf; grau 11 - 28%, (N = 7), de 31 a 45 eosinófilos/hpf e grau 111 »24%, (N = 6), com 46 ou mais eosinófilos/hpf.Os achados en»doscópicos do esôfago também foram analisados em 20 pacien»tes, com os seguintes resultados: em 15% dos casos, (N = 3), de»tectaram-se grumos brancacentos; em 5% dos casos, (N = 1), encontraram-se estrias longitudinais; em 15% dos casos, (N = 3), foram detectados anéis concêntricos (feline aspect); em 25% dos casos, (N = 5), registrou-se espessamento de mucosa; em 45% dos casos, (N = 8), encontrou-se esofagite erosiva e em 10%, (N = 2), encontrou-se estenose parcial. Observamos que a EE é uma entidade clínico-patológica caracterizada pela presença de eosinó»filos intra-epiteliais com contagem acima de 15 eosinófilos / hpf. As queixas clínicas e os aspectos endoscópicos podem direcionar o diagnóstico...

Asunto(s)

Humanos , Masculino , Femenino , Eosinofilia , Endoscopía/clasificación , Endoscopía/tendencias , Esofagitis/clasificación , Biopsia con Aguja , Hallazgos Incidentales , Laminas , Estudios Retrospectivos , Signos y Síntomas

RESUMEN

OBJETIVO: verificar a acuidade do exame citológico do colo uterino para o diagnóstico do HPV, comparado à reação em cadeia da polimerase (PCR), em amostras de mulheres portadoras do HIV. MÉTODOS: foram incluídas 158 pacientes, sendo realizada uma primeira coleta de material da cérvice uterina com a espátula de Ayre para a PCR. A seguir, foi realizada outra coleta com espátula de Ayre e escova para a citologia oncótica. Foram revisadas 109 lâminas, tendo em vista que 49 foram destruídas, por terem ultrapassado dois anos de arquivo. RESULTADOS: a prevalência de HPV foi de 11 por cento no estudo citológico e 69,7 por cento na PCR. A idade do grupo variou de 20 a 61 anos, com mediana de 35 anos. A forma de contágio pelo HIV foi a heterossexual em 91,8 por cento dos casos e 79,1 por cento dos pacientes tiveram um a cinco parceiros sexuais em toda a vida. A queixa mais freqüente foi massa pélvica (5,1 por cento) e 75,3 por cento procuraram o serviço para consulta de rotina. A comparação de variáveis categóricas foi realizada através de tabelas de contingência sendo utilizado o teste do χ2 com correção de Yates para comparação de proporções. Quando uma das freqüências esperadas foi menor que cinco, foi utilizado o teste de Fisher. Na comparação de testes diagnósticos foram calculados: a sensibilidade, a especificidade e razões de verossimilhança. Das 76 pacientes com HPV detectado pela PCR, somente 12 foram confirmadas pela citologia (sensibilidade=15,8 por cento) que, por outro lado, não apresentou resultados falsos-positivos (especificidade=100 por cento). Comparando-se os dois resultados, encontraram-se valor preditivo positivo de 100 por cento e negativo de 33,3 por cento para a citologia, na predição da presença do HPV. Entre as 12 pacientes com citologia positiva para HPV, quatro (33,3 por cento) apresentaram neoplasias intra-epiteliais cervicais (OR=5,6; razão de verossimilhança positiva=infinidade positiva; razão de verossimilhança...

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PURPOSE: to verify the accuracy of uterine cervix cytology for HPV diagnosis, as compared to polymerase chain reaction (PCR) in samples of women with HIV. METHODS: 158 patients who had undergone a first collection of material from the uterine cervix with Ayre's spatula for PCR were included in the study. Then, another collection with Ayre's spatula and brush for oncotic cytology was performed. Only 109 slides were reviewed, as 49 of them had already been destructed for have being filed for over two years. RESULTS: the prevalence of HPV was 11 percent in the cytological exam and 69.7 percent in the PCR. Age varied from 20 to 61 years old, median 35 years. The HIV contagious route was heterosexual in 91.8 percent of the cases, and 79.1 percent of the patients had had from one to five sexual partners along their lives. The most frequent complaint was pelvic mass (5.1 percent), and 75.3 percent of the women had looked for the service for a routine medical appointment. The categorical variable comparison was done through contingency tables, using the χ2 test with Yates's correction to compare the ratios. The Fisher's test was used when one of the expected rates was lower than five. In the comparison of diagnostic tests, sensitivity, specificity and similarity ratios have been calculated. Among the 76 patients with HPV, detected by PCR, only 12 had the diagnosis confirmed by cytology (sensitivity=15.8 percent), which on the other hand did not present any false-positive results (specificity=100 percent). Concerning the HPV presence, the cytological prediction for positive results was 100 percent and 33.3 percent for negative, when both results were compared. Among the 12 patients with HPV positive cytology, four (33.3 percent) presented cervical intraepithelial neoplasia (OR=56; positive similarity ratio=positive infinity; negative similarity ratio=0.83). CONCLUSIONS: As the cytology specificity is quite high, it is possible to rely on...

Asunto(s)

Adulto , Femenino , Humanos , Persona de Mediana Edad , Adulto Joven , Cuello del Útero/patología , Cuello del Útero/virología , Infecciones por VIH/complicaciones , Reacción en Cadena de la Polimerasa , Infecciones por Papillomavirus/complicaciones , Infecciones por Papillomavirus/patología , Reproducibilidad de los Resultados , Adulto Joven

RESUMEN

OBJECTIVE: To evaluate the effects of treatment on liver histopathology of children and adolescents diagnosed with autoimmune hepatitis. PATIENTS AND METHODS: Histopathological evaluation of liver biopsies performed at diagnosis or early during treatment, compared with biopsies after immunosuppressive treatment of 20 children and adolescents diagnosed with autoimmune hepatitis who presented clinical and biochemical remission for at least 24 months. Liver histopathology was assessed by 2 pathologists. Agreement between their interpretations was analyzed with kappa statistics. RESULTS: The age at diagnosis of the 20 patients varied from 1.7 years to 11.6 years (median = 6.6 years); 18 were females. The mean duration of clinical and biochemical remission, up to performance of liver biopsy, was 4.1 years. The mean interval between the initial and posttreatment biopsies was 4.6 years (range 2-9.7 years). Assessing the necroinflammatory activity, a mean reduction by 6.3 (observer 1) and 7.3 (observer 2) in the grading score was observed (P = 0.00000). When staging was assessed, a mean reduction by 1.8 (observers 1 and 2) in the score was observed after treatment (P = 0.00008), and there was no progression toward cirrhosis. No regression of cirrhosis was observed. CONCLUSIONS: On histopathological evaluation, the immunosuppressive treatment improved the fibrosis scores, with an arrest in its progression and no development into cirrhosis. Fibrosis control is mainly associated with regression of necroinflammatory activity, which is the main treatment component in autoimmune hepatitis.

Asunto(s)

Hepatitis Autoinmune/tratamiento farmacológico , Hepatitis Autoinmune/patología , Inmunosupresores/uso terapéutico , Hígado/patología , Biopsia con Aguja , Niño , Preescolar , Femenino , Hepatitis Autoinmune/diagnóstico , Humanos , Lactante , Cirrosis Hepática/patología , Masculino

RESUMEN

PURPOSE: to verify the accuracy of uterine cervix cytology for HPV diagnosis, as compared to polymerase chain reaction (PCR) in samples of women with HIV. METHODS: 158 patients who had undergone a first collection of material from the uterine cervix with Ayre's spatula for PCR were included in the study. Then, another collection with Ayre's spatula and brush for oncotic cytology was performed. Only 109 slides were reviewed, as 49 of them had already been destructed for have being filed for over two years. RESULTS: the prevalence of HPV was 11% in the cytological exam and 69.7% in the PCR. Age varied from 20 to 61 years old, median 35 years. The HIV contagious route was heterosexual in 91.8% of the cases, and 79.1% of the patients had had from one to five sexual partners along their lives. The most frequent complaint was pelvic mass (5.1%), and 75.3% of the women had looked for the service for a routine medical appointment. The categorical variable comparison was done through contingency tables, using the chi2 test with Yates's correction to compare the ratios. The Fisher's test was used when one of the expected rates was lower than five. In the comparison of diagnostic tests, sensitivity, specificity and similarity ratios have been calculated. Among the 76 patients with HPV, detected by PCR, only 12 had the diagnosis confirmed by cytology (sensitivity=15.8%), which on the other hand did not present any false-positive results (specificity=100%). Concerning the HPV presence, the cytological prediction for positive results was 100% and 33.3% for negative, when both results were compared. Among the 12 patients with HPV positive cytology, four (33.3%) presented cervical intraepithelial neoplasia (OR=56; positive similarity ratio=positive infinity; negative similarity ratio=0.83). CONCLUSIONS: As the cytology specificity is quite high, it is possible to rely on the positive result, which means that a positive result will surely indicate the presence of HPV. The low sensitivity of cytology does not qualify it as a survey exam for HPV detection in this female group.

Asunto(s)

Cuello del Útero/patología , Cuello del Útero/virología , Infecciones por VIH/complicaciones , Infecciones por Papillomavirus/complicaciones , Infecciones por Papillomavirus/patología , Reacción en Cadena de la Polimerasa , Adulto , Femenino , Humanos , Persona de Mediana Edad , Reproducibilidad de los Resultados , Adulto Joven

RESUMEN

Introdução: O diagnóstico de esôfago de Barrett (EB), única lesão de risco reconhecida para o adenocarcinoma do esôfago distal, tem merecido crescente importância. O objetivo foi avaliar morfológica e histoquimicamente o esôfago distal e a junção esôfago-gástrica numa série consecutiva de pacientes com refluxo gastroesofágico (AGE). Método: Estudaram-se 255 pacientes com AGE submetidos consecutivamente à endoscopia com biópsias, que foram processadas rotineiramente para diagnóstico em lâminas coradas por HE e PAS-Azul de Alciano. Classificou-se a metaplasia intestinal (MI) em tipos completo e incompleto. A presença de MI e de "células azuis" e caliciformes isoladas foi topografada e correlacionada com características demográficas e endoscópicas dos pacientes. Resultados: Identificou-se MI em 63 casos (25%), 57% localizados no esôfago e 9,5% na cárdia; em 35% dos casos a topografia não pôde ser definida em bases puramente morfológicas. Diagnosticou-se MI de tipo incompleto em 56 casos e de tipo completo em sete, seis dos quais localizados na cárdia. EB foi diagnosticado em 57 pacientes, predominantemente homens (p=0,003) e significativamente mais velhos que aqueles sem EB (p=0,001). Células Azul de Alciano positivas não caliciformes ("celulas azuis") estavam presentes em 87% dos casos, sem relação com EB. Conclusões: O EB foi frequente na série estudada, caracterizando-se por MI de tipo incompleto, enquanto a MI da cárdia foi predominantemente de tipo completo. As "células azuis" são alterações indefinidas quanto ao seu papel na gênese do EB. A utilização de protocolos endoscópico-histológicos pode contribuir para a acuidade diagnóstica do EB.

Asunto(s)

Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Esófago de Barrett/diagnóstico , Intestinos/patología , Biopsia , Unión Esofagogástrica , Metaplasia , Reflujo Gastroesofágico

RESUMEN

OBJETIVO: avaliar a associação entre a contagem de linfócitos T CD4+ e a gravidade da neoplasia intra-epitelial cervical em pacientes HIV positivas. MÉTODOS: estudo transversal no qual foram incluídas 87 pacientes infectadas pelo HIV, confirmado por testes sorológicos prévios. Todas eram portadoras do HPV cervical, diagnosticado por meio da reação em cadeia da polimerase. Foram realizados anamnese, exame físico e colposcopia de todas em pacientes. A biópsia do colo uterino foi realizada quando indicada pelo exame colposcópico. Os resultados histopatológicos foram classificados com neoplasia intra-epitelial de baixo grau (NIC I) ou de alto grau (NIC II e II). A associação entre a contagem de linfócitos T CD4+ e a gravidade da lesão foi verificada por meio da comparação de médias utilizando a análise da variância (ANOVA). RESULTADOS: entre as 60 pacientes biopsiadas foram encontrados 24 casos (40,0 por cento) com NIC I, oito (13,3 por cento) NIC II, três (5 por cento) NIC III, 14 (23,3 por cento) pacientes somente com cervicite crônica e 11 (18,3 por cento) apresentando efeito citopático produzido pelo HPV, mas sem perda da polaridade celular. Isso equivale a 35 mulheres com lesão intra-epitelial de baixo grau (NIC I + HPV) (58,3 por cento) e 11 (18,3 por cento) com lesão intra-epitelial de alto grau (NIC II + NIC III). A associação entre a média da contagem de linfócitos T CD4+ e a gravidade da lesão intra-epitelial cervical não foi significativa (p=0,901). CONCLUSÕES: não houve associação entre a contagem de linfócitos T CD4+ e a gravidade da lesão intra-epitelial do colo uterino, diagnosticada pelo exame histopatológico.

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PURPOSE: to evaluate association between CD4+ cell count and cervical intraepithelial lesion severity in HIV-infected women. METHODS: cross-sectional study of 87 HIV-infected patients which were confirmed by previous serologic examinations. All had cervical HPV diagnosed by polymerase chain reaction (PCR). All patients underwent anamnesis, physical examinations and colposcopy. Cervix biopsy was performed when indicated by colposcopical examination. Histopathological results followed Richart's classification, adapted by Wright, and CD4+ cell count and cervical intraepithelial lesion severity association was analysed by comparison of means using analysis using analysis of variance (ANOVA). RESULTS: among 60 biopsied women 24 were found (40.0 percent) with CIN I, eight (13.3 percent) with CIN II, three (5 percent) with CIN III, 14 (23.3 percent) with chronic cervicitis and 11 with cytopathic effect of HPV, without cell polarity loss. This corresponds to 35 (58.3 percent) women with intraepithelial lesion of low grade (CIN I + HPV) and 11 (18.3 percent) with intraepithelial lesion of high grade (CIN II + CIN III). There was no significant association between CD4+ cell count mean and cervical intraepithelial lesion severity (p=0.901). CONCLUSIONS: there was no association between CD4+ cell count and cervical intraepithelial lesion severity diagnosed by histopathological examination.

Asunto(s)

Adolescente , Adulto , Persona de Mediana Edad , Humanos , Femenino , Síndrome de Inmunodeficiencia Adquirida , Displasia del Cuello del Útero , Sondas de ADN de HPV , Infecciones por VIH , Neoplasias del Cuello Uterino

RESUMEN

A gastroenterite eosinofílica (GE) é considerada uma doença pouco comum, com menos de 300 casos relatados na literatura. É caracterizada por infiltração eosinofílica das camadas da parede do tubo digestivo. A patogênese não é bem conhecida. Há algumas evidências da participação de fatores imunológicos ou alérgicos. Em geral, o prognóstico é favorável, embora a doença tenha caráter recorrente. Relata-se o caso de paciente, 21 anos, sexo masculino/ que apresentou quadro de dor abdominal, náusea, vômitos, emagrecimento e eliminação reduzida de flatos e fezes. Ao exame físico, foram observadas distensão abdominal, dor à palpação e ascite tensa. Os exames laboratoriais demonstraram eosinofilia no sangue periférico, variando de 15 a 60%. Exames parasitológicos de fezes seriados não mostraram ovos ou larvas. Ao estudo radiológico, identificaram-se espessamento da parede do intestino delgado e redução do lume. Infiltração eosinofílica da mucosa do cólon distal foi verificada pelo exame anatomopatológico. Com base nesses achados, o diagnóstico de GEfoi realizado e instituído o tratamento com prednisona, ocorrendo remissão da doença. Apesar de ser considerada doença rara e de causa ainda desconhecida, a GEdeve ser incluída no diagnóstico diferencial dos quadros de eosinofilia periférica com comprometimento do trato gastrintestinal (TGI).

Asunto(s)

Humanos , Masculino , Adulto , Ascitis/sangre , Gastroenteritis/tratamiento farmacológico , Síndrome Hipereosinofílico , Seudoobstrucción Intestinal , Biopsia , Colonoscopía , Cetotifen/uso terapéutico , Ciclofosfamida/uso terapéutico , Ciclosporina/uso terapéutico , Corticoesteroides/uso terapéutico , Examen Físico , Recurrencia , Signos y Síntomas , Tiabendazol/uso terapéutico

RESUMEN

BACKGROUND: Helicobacter species are associated with inflammatory bowel disease in rodents and in nonhuman primates. Therefore, we prospectively investigated the presence of Helicobacter species in the intestinal mucosa of patients with and without Crohn's disease by culture and polymerase chain reaction (PCR) assays. MATERIALS AND METHODS: Mucosal fragments were obtained from the ileum, different colon regions, and rectum of 43 patients with Crohn's disease and of 74 patients without inflammatory bowel disease. RESULTS: Helicobacter pylori strains, identified by 16S rRNA gene sequencing, were more frequently isolated and PCR-detected in the intestinal mucosa of patients with ulcerative colitis-like Crohn's disease than in intestinal mucosa of the control group. Otherwise, anti-H. pylori immunoglobulin G levels were significantly lower in fibrostenosing and fistulating Crohn's disease subgroups. No other Helicobacter species were found in the intestinal mucosa of the patients. CONCLUSIONS: Although our results suggest an association between the presence of H. pylori in the intestine and ulcerative colitis-like phenotype of Crohn's disease, H. pylori infection in the actual causality of Crohn's disease is still to be determined.

Asunto(s)

Enfermedad de Crohn/microbiología , Helicobacter pylori/aislamiento & purificación , Mucosa Intestinal/microbiología , Adolescente , Adulto , Anciano , Estudios de Casos y Controles , Enfermedad de Crohn/etiología , ADN Bacteriano/análisis , Femenino , Infecciones por Helicobacter/microbiología , Helicobacter pylori/genética , Humanos , Inmunoglobulina G/análisis , Masculino , Persona de Mediana Edad , Reacción en Cadena de la Polimerasa/métodos , ARN Ribosómico 16S/genética

RESUMEN

OBJECTIVE: To assess treatment withdrawal in children and adolescents with autoimmune hepatitis, with clinical and laboratory remission for a minimum period of 24 months, determining the relapse rate after treatment withdrawal. METHODS: This is a descriptive, retrospective and partially prospective study of 21 children and adolescents with type 1 autoimmune hepatitis treated at the Outpatient Division of Pediatric Hepatology, Teaching Hospital of Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Brazil, between January 1986 and December 2001. RESULTS: We assessed 54 patients and selected 21, of whom 19 were female subjects (90.5%), aged between 5.7 and 17.6 years (median = 13.8 years), with a mean follow-up of 5.1+/-2.4 years (median = 4.4 years) and an average clinical and laboratory remission of 4.1+/-1.5 years (median = 4.1 years). Out of the 21 patients studied, 10 (47.6%) manifested some inflammatory activity that prevented the discontinuation of treatment, which was withdrawn in 11 patients (52.4%). Out of these, six patients (54.5%) presented reactivation of the disease and five maintained clinical and laboratory remission with a mean follow-up of 4+/-1 years (median = 3.9 years). The time interval between discontinuation of treatment and reactivation of the disease ranged from 29 days to 40.3 months (median = 2.2 months). CONCLUSIONS: We observed a high relapse rate (54.5%) in this group of patients with autoimmune hepatitis, which was more frequent within the first 12 months after treatment withdrawal, in addition to a high number of patients that presented some degree of inflammatory activity despite the long period of clinical and laboratory remission.

Asunto(s)

Hepatitis Autoinmune/patología , Inmunosupresores/uso terapéutico , Hígado/patología , Privación de Tratamiento , Adolescente , Biopsia , Niño , Preescolar , Métodos Epidemiológicos , Femenino , Hepatitis Autoinmune/tratamiento farmacológico , Humanos , Lactante , Masculino , Recurrencia , Inducción de Remisión , Factores de Tiempo