966 resultados para ALVEOLAR ATTACHMENTS
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Numerous pulmonary schistosome egg granulomas were present in mice submitted to partial portal vein ligation (Warren's model). The granulomas were characterized by cellular aggregations formed within alveolar tissue. Main cellular types were macrophages (epithelioid cells), eosinophils, plasma cells and lymphocytes. These cells were supported by scanty fibrous stroma and exhibited close membrane contact points amongst themselves, but without forming specialized adhesion apparatus. When granulomas involved arterial structures, proliferation of cndothelial and smooth muscle cells occurred and fibrosis associated with angiogenesis became more evident. Granulomas formed around mature eggs in the pulmonary alveolar tissue presented approximately the same size and morphology regardless of the time of infection, the latter being 10, 18 and 25 weeks after cercarial exposure. This persistence of morphological appearance suggests that pulmonary granulomas do not undergo immunological modulation, as is the case with the granulomas in the liver and, to a lesser extent, in the intestines. Probably, besides general immunological factors, local (stromal) factors play an important role in schistosomal granuloma modulation.
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The authors studied 58 infants hospitalized for pneumonia in a semi-intensive care unit. Age ranged from 1 complete to 6 incomplete months. The infants were sent from another hospital in 20 cases and from home in a further 38. Pulmonary involvement, which was alveolar in 46 cases and interstitial in 12, was bilateral in 31 children. The investigation was carried out prospectively on the etiological agents associated with respiratory infection to look for evidence of aerobic bacteria (blood cultures), Chlamydia trachomatis and Cytomegalovirus (serology), and Pneumocystis carinii (direct microscopy of tracheal aspirated material). The following infectious agents were diagnosed in 21 children (36.2%): Aerobic bacteria (8), Chlamydia trachomatis (5), Pneumocystis carinii (3), Cytomegalovirus (3), Cytomegalovirus and Chlamydia trachomatis (1), Aerobic bacteria and Cytomegalovirus (1). Seven cases of infection by Chlamydia trachomatis and/or Cytomegalovirus were diagnosed out of the 12 cases with pulmonary interstitial involvement.
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Three cases of the juvenile form of paracoccidioidomycosis are reported. Emphasis has been given to the oral manifestations, particularly the periodontal involvement. The main periodontal findings were: generalized and progressive alveolar bone destruction leading to gingival recession with exposure of the tooth roots, and spontaneous tooth losses. The gingival mucosa was predominantly smooth, erithematous and slightly swollen. These aspects, although rare, may be the earliest signs of the disease and sometimes its only manifestation.
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Hantavirus pulmonary syndrome (HPS) has been recognized recently in Brazil, where 28 cases have been reported as of September 1999. We report here the clinical and laboratory findings of three cases whose diagnoses were confirmed serologically. All the patients were adults who presented a febrile illness with respiratory symptoms that progressed to respiratory failure that required artificial ventilation in two of them. Laboratory findings were most of the time consistent with those reported in the United States in patients infected with the Sin Nombre virus, and included elevated hematocrit and thrombocytopenia; presence of atypical lymphocytes was observed in one patient. The chest radiological findings observed in all the patients were bilateral, diffuse, reticulonodular infiltrates. Two patients died. Histopathological examination of the lungs of these patients revealed interstitial and alveolar edema, alveolar hemorrhage, and mild interstitial pneumonia characterized by infiltrate of immunoblasts and mononuclear cells. In the epidemiologic investigation of one of the cases, serologic (ELISA) tests were positive in 3 (25%) out of 12 individuals who shared the same environmental exposure. HPS should be included in the differential diagnosis of interstitial pneumonia progressing to acute respiratory failure.
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The respiratory viruses are recognized as the most frequent lower respiratory tract pathogens for infants and young children in developed countries but less is known for developing populations. The authors conducted a prospective study to evaluate the occurrence, clinical patterns, and seasonal trends of viral infections among hospitalized children with lower respiratory tract disease (Group A). The presence of respiratory viruses in children's nasopharyngeal was assessed at admission in a pediatric ward. Cell cultures and immunofluorescence assays were used for viral identification. Complementary tests included blood and pleural cultures conducted for bacterial investigation. Clinical data and radiological exams were recorded at admission and throughout the hospitalization period. To better evaluate the results, a non- respiratory group of patients (Group B) was also constituted for comparison. Starting in February 1995, during a period of 18 months, 414 children were included- 239 in Group A and 175 in Group B. In Group A, 111 children (46.4%) had 114 viruses detected while only 5 children (2.9%) presented viruses in Group B. Respiratory Syncytial Virus was detected in 100 children from Group A (41.8%), Adenovirus in 11 (4.6%), Influenza A virus in 2 (0.8%), and Parainfluenza virus in one child (0.4%). In Group A, aerobic bacteria were found in 14 cases (5.8%). Respiratory Syncytial Virus was associated to other viruses and/or bacteria in six cases. There were two seasonal trends for Respiratory Syncytial Virus cases, which peaked in May and June. All children affected by the virus were younger than 3 years of age, mostly less than one year old. Episodic diffuse bronchial commitment and/or focal alveolar condensation were the clinical patterns more often associated to Respiratory Syncytial Virus cases. All children from Group A survived. In conclusion, it was observed that Respiratory Syncytial Virus was the most frequent pathogen found in hospitalized children admitted for severe respiratory diseases. Affected children were predominantly infants and boys presenting bronchiolitis and focal pneumonias. Similarly to what occurs in other subtropical regions, the virus outbreaks peak in the fall and their occurrence extends to the winter, which parallels an increase in hospital admissions due to respiratory diseases.
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Eighteen mongrel dogs of unknown age and naturally infected with Leishmania (Leishmania) chagasi, were obtained from the City Hall of Belo Horizonte, Brazil. Four dogs were used as control. Lung samples were obtained and immediately fixed in formalin. The histopathological picture of all lung tissue sections was a chronic and diffuse interstitial pneumonitis. The thickened inter-alveolar septa were characterized by the cellular exudate (mostly macrophages, lymphocytes and plasmocytes) associated with collagen deposition. Morphometric analysis showed greater septal thickness in the infected animals than in controls. In fact, the morphometric study of collagen stained with ammoniac silver confirmed a larger deposition of collagen in the infected animals. The parasitologic method was carried out during the study of the lesions on the slides. However, we did not observe any correlation between the histopathologic and morphometric data and the clinical status of the animals. We conclude that the pulmonary lesions observed in all naturally infected dogs were correlated with the disease and that the morphometric method used was satisfactory for the analysis of septal thickness and of increased collagen deposition, confirming the presence of fibrosis.
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In order to determine the role of lysozyme, an antimicrobial peptide belonging to the innate immune system, against the dimorphic fungus Paracoccidioides brasiliensis, co-cultures of the MH-S murine alveolar macrophages cell line with P. brasiliensis conidia were done; assays to evaluate the effect of physiological and inflammatory concentrations of lysozyme directly on the fungus life cycle were also undertaken. We observed that TNF-α-activated macrophages significantly inhibited the conidia to yeast transition (p = 0.0043) and exerted an important fungicidal effect (p = 0.0044), killing 27% more fungal propagules in comparison with controls. Nonetheless, after adding a selective inhibitor of lysozyme, the fungicidal effect was reverted. When P. brasiliensis propagules were exposed directly to different concentrations of lysozyme, a dual effect was observed. Physiologic concentrations of the enzyme facilitated the conidia-to-yeast transition process (p < 0.05). On the contrary, inflammatory concentrations impaired the normal temperature-dependant fungal transition (p < 0.0001). When yeast cells were exposed to lysozyme, irrespective of concentration, the multiple-budding ability was badly impaired (p < 0.0001). In addition, ultra-structural changes such as subcellular degradation, fusion of lipid vacuoles, lamellar structures and interruption of the fibrilar layer were observed in lysozyme exposed conidia. These results suggest that lysozyme appears to exert a dual role as part of the anti-P. brasiliensis defense mechanisms.
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Introdução: Actualmente, a maioria dos casos pediátricos de infecção por VIH é devida a transmissão materna do vírus. Na ausência de medidas de profilaxia, verificam se taxas de transmissão vertical do VIH-1 entre 15-25% na Europa Ocidental e Estados Unidos, 65% dos casos no peri-parto, 23% in útero e 12% no período pós-natal durante a amamentação. Caso clínico: Criança de 9 anos, sexo feminino, que recorre à urgência por febre, anorexia e tumefacção cervical com 2 dias de evolução. Dos antecedentes pessoais há a destacar: gravidez não vigiada, parto eutócico de termo, aleitamento materno até aos 3 anos e atraso do desenvolvimento estaturo-ponderal. Antecedentes patológicos de parotidite bilateral aos 5 anos e múltiplas cáries dentárias. À observação apresentava-se febril, emagrecida (peso < P5 e estatura no P5), com tumefacção cervical e retroauricular direitas, e aumento de volume das glândulas parótidas. Sem hepatoesplenomegalia e sem adenopatias palpáveis nas restantes cadeias ganglionares periféricas. Analíticamente, VS de 90 mm/h, sem outras alterações relevantes. Ecografia cervical mostrou adenofleimão e alterações compatíveis com parotidite. Internada com a hipótese diagnóstica de adenofleimão cervical e medicada com penicilina e clindamicina endovenosas (ev). Realizou serologias para VIH, com positividade para VIH tipo 1, confirmado por Western Blot. Contagem de linfócitos T CD4+ de 240 células/mm3. Carga viral de 3,82 x 103 cópias de RNA/mL. Genótipo HLA-B*5701 negativo. Confirmada infecção VIH 1 materna por Western Blot. Diagnóstico prévio de infecção VIH no período neonatal ocultado pela mãe. Restantes serologias negativas, assim como a pesquisa de BK no suco gástrico e o estudo do lavado bronco-alveolar. Ao 17º dia de internamento foi realizada punção do adenofleimão e alterada a antibioticoterapia para flucloxacilina ev (7 dias de terapêutica). Pesquisa de micobactérias e fungos no pús drenado negativa. Durante o internamento manteve-se clinicamente estável, iniciando profilaxia para Pneumocystis jirovecii com cotrimoxazol, e terapêutica anti-retroviral (Lamivudina, Abacavir, Lopinavir/Ritonavir), com melhoria clínica, virulógica e imunológica. Conclusões: Este caso ilustra um exemplo de transmissão vertical do VIH-1 caracterizado por uma evolução crónica, cuja apresentação cursou com parotidite, um dos sinais indicadores de infecção VIH.
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Introdução: Os doentes com Imunodeficiência Combinada Grave (SCID) não diagnosticados evoluem inexoravelmente para a morte no primeiro ano de vida. Um elevado índice de suspeição é fundamental para o diagnóstico precoce, o factor mais importante para a sobrevida destas crianças. Objectivo: Apresentam-se três casos clínicos ilustrativos da importância da precocidade diagnóstica no prognóstico final. Casos clínicos: Caso clínico 1: Lactente do sexo masculino, com antecedentes de infecções respiratórias de repetição, internado aos sete meses na UCIP do HDE por pneumonia a Adenovírus com insuficiência respiratória. Necessitou de ventilação mecânica e de duas transfusões de concentrado eritrocitário na primeira semana de internamento. Teve exantema exuberante, interpretado como toxidermia. Evoluiu para doença pulmonar sequelar grave. Aos nove meses foi feito o diagnóstico de SCID hipomorfa com doença do enxerto contra o hospedeiro pós-transfusional, controlada com imunossupressão (ciclosporina e glucocorticoides). Não foi transplantado com células progenitoras hematopoiéticas por não reunir condições clínicas. Na sequência de uma intercorrência respiratória veio a falecer aos 14 meses. Caso clínico 2: Lactente do sexo masculino, internado aos 6 meses no HDE por pneumonia intersticial hipoxemiante. Isolado P. jiroveci no lavado bronco-alveolar e feito o diagnóstico presuntivo de BCGite disseminado em criança com SCID T-B+NK-. Após estabilização clínica e esplenectomia foi transplantado com células progenitoras hematopoiéticas de dador fenoidêntico não aparentado. Dada a BCGite disseminada necessitou de vários ciclos de infusão de células do dador para uma reconstituição imunitária lenta e progressiva. Seis meses pós-transplante está clinicamente bem, com quimerismo linfóide T e NK completo. Caso clínico 3: Lactente do sexo masculino, internado aos 17 dias de vida por infecção respiratória alta e bacteriémia a M. catarrhalis. Reinternado quinze dias depois por sépsis a MRSA e linfopénia. A avaliação efectuada permitiu o diagnóstico de SCID T-B+NK- por defeito na cadeia gamma comum. Transplantado com células progenitoras hematopoiéticas de dador genoidêntico aos 4 meses, sem condicionamento. Clinicamente bem, seis meses pós-transplante, com reconstituição imunitária satisfatória. Conclusão: Esta doença tem uma prevalência não negligenciável e apenas com elevado indice de suspeição se pode estabelecer um plano de tratamento eficaz.
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The use of minimally invasive surgery for the treatment of lung cancer has been growing worldwide. Between May 2008 and November 2012, we performed 24 videothoracoscopic anatomical lung resections in our department. This includes 22 lobectomies and 2 anatomic segmentectomies, which is known to be a more complex surgery, since it demands a finer dissection of sub-lobar structures. We report the clinical cases of two patients who underwent anatomic segmentectomies. The first one was a 63 year old woman, smoker and with a history of breast cancer 20 years earlier. An incidental 9 mm node was found in the lingula. The patient underwent an anatomic lingulectomy and the frozen section was suggestive of a primary lung cancer. Therefore, we proceeded to a full lymphadenectomy. The final pathology evaluation showed a typical carcinoid tumour (pT1aN0). The second patient was a 50 year old woman, a smoker and with a heavy family history of lung cancer. In a screening CT scan a 8 mm ground glass opacity was identified in the left lower lobe (segment VI). After a VATS wedge resection of the node the frozen section evaluation was compatible with adenocarcinoma. We then proceeded to an anatomic segmentectomy with lymphadenectomy. The definitive pathology evaluation confirmed that it was a pT1a N0 bronchioloalveolar adenocarcinoma. The patients now have 5 and 2 months of follow up respectivelly and neither of them has signs of recurrence and the surgical incision showed a good aesthetic result. Anatomic segmentectomy is the indicated surgery especially in patients with low grade tumours, in early stage lung cancers or in patients without pulmonary function for a lobar resection, and it can be done safely using VATS.
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Dissertação para obtenção do Grau de Mestre em Engenharia Mecânica
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Dissertação para obtenção do Grau de Mestre em Engenharia Biomédica
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Propylthiouracil (PTU) is known to induce antineutrophil cytoplasmatic antibody (ANCA) seropositivity; however, small vessel vasculitis (SVV) with pulmonary and renal involvement is rare. We present the case of an 81-year-old woman on PTU treatment due to toxic nodular goitre who developed alveolar hemorrhage and rapidly progressive glomerulonephritis. The authors highlight the importance of early recognising drug-induced pulmonary-renal syndrome (PRS) in order to avoid unnecessary tests, a delay in the diagnosis and evolution to end-stage kidney disease or life-threatening conditions.
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Em 23 pacientes com leptospirose apresentando comprometimento pulmonar, internados no Hospital Universitário Antônio Pedro da XJFF, Niterói, hemoptise e hemoptóicos foram observados em 21,7% e 30,4%, respectivajnente. Gasometria arterial revelou hipoxemia e hipocapnia na maioria dos casos. Radiografia de tórax em 15 pacientes mostrou comprometimento alveolar em 60%, comprometimento intersticial-reticular em 6%, padrão misto (alveolar e intersticial) em20%e ausência de alterações radiológicas em 14%. A necrópsiade 13 pacientes mostrou edema, congestão e hemorragia nos pulmões em 100% dos casos. A hemorragia foi focal em 46% e difusa em 54% dos casos. Houve formação de membrana hialina em 30% e trombos de fibrina em 46% dos pulmões estudados, o que estabelece o diagnóstico da coagulação intravascular disseminada e a ocorrência da síndrome de angústia respiratória na leptospirose.
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Dissertação para obtenção do Grau de Mestre em Engenharia da Soldadura