Haemorrhagic syndrome of Altamira

Detalhes bibliográficos
Autor(a) principal: Pinheiro, Francisco de Paula
Data de Publicação: 1974
Outros Autores: Bensabath, Gilberta, Costa Junior, Domingos, Maroja, Octavio M, Lins, Zéa Constante, Andrade, Amélia Homobono Paes de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Digital do Instituto Evandro Chagas (Patuá)
Texto Completo: https://patua.iec.gov.br/handle/iec/351
Resumo: Since January, 1972, a haemorrhagic mary syndrome has been observed among immigrants living in forested areas along the newly opened Transamazon Highway in Brazil. Most cases are found around Altamira. The illness is characterised by localised and disseminated cutaneous hremorrhages, which are associated with mucosal bleeding in 32 % of patients. Platelet-counts are reduced, and there is prolonged bleeding-time and poor clot retraction in about half of the cases. The illness was diagnosed as thrombocytopenic purpura. Familial clustering of cases was found, with more children being involved than adults. A few deaths have been attributed to the disease. The precise aetiology of this condition remains obscure. Drugs, alimentary factors, and various viral, rickettsial, and bacterial pathogens do not seem to be involved. Epidemiological and serological evidence suggests that the syndrome is associated with the black-fly, Simulium, and its bite. Case-lates in the Altamira region began to rise shortly after the appearance of large numbers of simulidre in the rainy season, and fell with the approach of the dry season and virtual disappearance af black-flies. Colonists in this area repon intense black-fly biting during the rainy season. The syndrome is not seen among natives of the region, most of whom live in the city of Altamira, where simulidz are much less common. Patients responded rapidly to steroid therapy, with platelet-counts returning to normal within a few days. The disorder has been named the hremorrhagic syndrome of Altamira.
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spelling Pinheiro, Francisco de PaulaBensabath, GilbertaCosta Junior, DomingosMaroja, Octavio MLins, Zéa ConstanteAndrade, Amélia Homobono Paes de2016-01-26T11:22:35Z2016-01-26T11:22:35Z1974PINHEIRO FILHO, Francisco de Paula et al. Haemorrhagic syndrome of Altamira. Lancet, n. 7859, p. 639-642, 1974.0140-6736https://patua.iec.gov.br/handle/iec/351Since January, 1972, a haemorrhagic mary syndrome has been observed among immigrants living in forested areas along the newly opened Transamazon Highway in Brazil. Most cases are found around Altamira. The illness is characterised by localised and disseminated cutaneous hremorrhages, which are associated with mucosal bleeding in 32 % of patients. Platelet-counts are reduced, and there is prolonged bleeding-time and poor clot retraction in about half of the cases. The illness was diagnosed as thrombocytopenic purpura. Familial clustering of cases was found, with more children being involved than adults. A few deaths have been attributed to the disease. The precise aetiology of this condition remains obscure. Drugs, alimentary factors, and various viral, rickettsial, and bacterial pathogens do not seem to be involved. Epidemiological and serological evidence suggests that the syndrome is associated with the black-fly, Simulium, and its bite. Case-lates in the Altamira region began to rise shortly after the appearance of large numbers of simulidre in the rainy season, and fell with the approach of the dry season and virtual disappearance af black-flies. Colonists in this area repon intense black-fly biting during the rainy season. The syndrome is not seen among natives of the region, most of whom live in the city of Altamira, where simulidz are much less common. Patients responded rapidly to steroid therapy, with platelet-counts returning to normal within a few days. The disorder has been named the hremorrhagic syndrome of Altamira.Ministério da Saúde. Fundação Instituo Oswaldo Cruz. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Fundação Instituo Oswaldo Cruz. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Fundação Instituo Oswaldo Cruz. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Fundação Instituo Oswaldo Cruz. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Fundação Instituo Oswaldo Cruz. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Fundação Instituo Oswaldo Cruz. Instituto Evandro Chagas. 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dc.title.pt_BR.fl_str_mv Haemorrhagic syndrome of Altamira
title Haemorrhagic syndrome of Altamira
spellingShingle Haemorrhagic syndrome of Altamira
Pinheiro, Francisco de Paula
Púrpura Trombocitopênica / diagnóstico
Púrpura Trombocitopênica / quimioterapia
Simuliidae / patogenicidade
Brasil (BR)
Altamira (PA)
title_short Haemorrhagic syndrome of Altamira
title_full Haemorrhagic syndrome of Altamira
title_fullStr Haemorrhagic syndrome of Altamira
title_full_unstemmed Haemorrhagic syndrome of Altamira
title_sort Haemorrhagic syndrome of Altamira
author Pinheiro, Francisco de Paula
author_facet Pinheiro, Francisco de Paula
Bensabath, Gilberta
Costa Junior, Domingos
Maroja, Octavio M
Lins, Zéa Constante
Andrade, Amélia Homobono Paes de
author_role author
author2 Bensabath, Gilberta
Costa Junior, Domingos
Maroja, Octavio M
Lins, Zéa Constante
Andrade, Amélia Homobono Paes de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Pinheiro, Francisco de Paula
Bensabath, Gilberta
Costa Junior, Domingos
Maroja, Octavio M
Lins, Zéa Constante
Andrade, Amélia Homobono Paes de
dc.subject.decsPrimary.pt_BR.fl_str_mv Púrpura Trombocitopênica / diagnóstico
Púrpura Trombocitopênica / quimioterapia
Simuliidae / patogenicidade
Brasil (BR)
Altamira (PA)
topic Púrpura Trombocitopênica / diagnóstico
Púrpura Trombocitopênica / quimioterapia
Simuliidae / patogenicidade
Brasil (BR)
Altamira (PA)
description Since January, 1972, a haemorrhagic mary syndrome has been observed among immigrants living in forested areas along the newly opened Transamazon Highway in Brazil. Most cases are found around Altamira. The illness is characterised by localised and disseminated cutaneous hremorrhages, which are associated with mucosal bleeding in 32 % of patients. Platelet-counts are reduced, and there is prolonged bleeding-time and poor clot retraction in about half of the cases. The illness was diagnosed as thrombocytopenic purpura. Familial clustering of cases was found, with more children being involved than adults. A few deaths have been attributed to the disease. The precise aetiology of this condition remains obscure. Drugs, alimentary factors, and various viral, rickettsial, and bacterial pathogens do not seem to be involved. Epidemiological and serological evidence suggests that the syndrome is associated with the black-fly, Simulium, and its bite. Case-lates in the Altamira region began to rise shortly after the appearance of large numbers of simulidre in the rainy season, and fell with the approach of the dry season and virtual disappearance af black-flies. Colonists in this area repon intense black-fly biting during the rainy season. The syndrome is not seen among natives of the region, most of whom live in the city of Altamira, where simulidz are much less common. Patients responded rapidly to steroid therapy, with platelet-counts returning to normal within a few days. The disorder has been named the hremorrhagic syndrome of Altamira.
publishDate 1974
dc.date.issued.fl_str_mv 1974
dc.date.accessioned.fl_str_mv 2016-01-26T11:22:35Z
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dc.identifier.citation.fl_str_mv PINHEIRO FILHO, Francisco de Paula et al. Haemorrhagic syndrome of Altamira. Lancet, n. 7859, p. 639-642, 1974.
dc.identifier.uri.fl_str_mv https://patua.iec.gov.br/handle/iec/351
dc.identifier.issn.-.fl_str_mv 0140-6736
identifier_str_mv PINHEIRO FILHO, Francisco de Paula et al. Haemorrhagic syndrome of Altamira. Lancet, n. 7859, p. 639-642, 1974.
0140-6736
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