Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease

Detalhes bibliográficos
Autor(a) principal: Romão,E.A.
Data de Publicação: 2006
Outros Autores: Moysés Neto,M., Teixeira,S.R., Muglia,V.F., Vieira-Neto,O.M., Dantas,M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Medical and Biological Research
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2006000400014
Resumo: The objective of the present study was to determine the frequency of the most common clinical features in patients with autosomal dominant polycystic kidney disease in a sample of the Brazilian population. The medical records of 92 patients with autosomal dominant polycystic kidney disease attended during the period from 1985 to 2003 were reviewed. The following data were recorded: age at diagnosis, gender, associated clinical manifestations, occurrence of stroke, age at loss of renal function (beginning of dialysis), and presence of a family history. The involvement of abdominal viscera was investigated by ultrasonography. Intracranial alterations were prospectively investigated by magnetic resonance angiography in 42 asymptomatic patients, and complemented with digital subtraction arteriography when indicated. Mean age at diagnosis was 35.1 ± 14.9 years, and mean serum creatinine at referral was 2.4 ± 2.8 mg/dL. The most frequent clinical manifestations during the disease were arterial hypertension (63.3%), lumbar pain (55.4%), an abdominal mass (47.8%), and urinary infection (35.8%). Loss of renal function occurred in 27 patients (mean age: 45.4 ± 9.5 years). The liver was the second organ most frequently affected (39.1%). Stroke occurred in 7.6% of the patients. Asymptomatic intracranial aneurysm was detected in 3 patients and arachnoid cysts in 3 other patients. In conclusion, the most common clinical features were lumbar pain, arterial hypertension, abdominal mass, and urinary infection, and the most serious complications were chronic renal failure and stroke. Both intracranial aneurysms and arachnoid cysts occurred in asymptomatic patients at a frequency of 7.14%.
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spelling Renal and extrarenal manifestations of autosomal dominant polycystic kidney diseaseAutosomal dominant polycystic kidney diseaseHepatic cystIntracranial aneurysmArachnoid cystEnd-stage renal diseaseThe objective of the present study was to determine the frequency of the most common clinical features in patients with autosomal dominant polycystic kidney disease in a sample of the Brazilian population. The medical records of 92 patients with autosomal dominant polycystic kidney disease attended during the period from 1985 to 2003 were reviewed. The following data were recorded: age at diagnosis, gender, associated clinical manifestations, occurrence of stroke, age at loss of renal function (beginning of dialysis), and presence of a family history. The involvement of abdominal viscera was investigated by ultrasonography. Intracranial alterations were prospectively investigated by magnetic resonance angiography in 42 asymptomatic patients, and complemented with digital subtraction arteriography when indicated. Mean age at diagnosis was 35.1 ± 14.9 years, and mean serum creatinine at referral was 2.4 ± 2.8 mg/dL. The most frequent clinical manifestations during the disease were arterial hypertension (63.3%), lumbar pain (55.4%), an abdominal mass (47.8%), and urinary infection (35.8%). Loss of renal function occurred in 27 patients (mean age: 45.4 ± 9.5 years). The liver was the second organ most frequently affected (39.1%). Stroke occurred in 7.6% of the patients. Asymptomatic intracranial aneurysm was detected in 3 patients and arachnoid cysts in 3 other patients. In conclusion, the most common clinical features were lumbar pain, arterial hypertension, abdominal mass, and urinary infection, and the most serious complications were chronic renal failure and stroke. Both intracranial aneurysms and arachnoid cysts occurred in asymptomatic patients at a frequency of 7.14%.Associação Brasileira de Divulgação Científica2006-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2006000400014Brazilian Journal of Medical and Biological Research v.39 n.4 2006reponame:Brazilian Journal of Medical and Biological Researchinstname:Associação Brasileira de Divulgação Científica (ABDC)instacron:ABDC10.1590/S0100-879X2006000400014info:eu-repo/semantics/openAccessRomão,E.A.Moysés Neto,M.Teixeira,S.R.Muglia,V.F.Vieira-Neto,O.M.Dantas,M.eng2006-04-03T00:00:00Zoai:scielo:S0100-879X2006000400014Revistahttps://www.bjournal.org/https://old.scielo.br/oai/scielo-oai.phpbjournal@terra.com.br||bjournal@terra.com.br1414-431X0100-879Xopendoar:2006-04-03T00:00Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)false
dc.title.none.fl_str_mv Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
title Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
spellingShingle Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
Romão,E.A.
Autosomal dominant polycystic kidney disease
Hepatic cyst
Intracranial aneurysm
Arachnoid cyst
End-stage renal disease
title_short Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
title_full Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
title_fullStr Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
title_full_unstemmed Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
title_sort Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease
author Romão,E.A.
author_facet Romão,E.A.
Moysés Neto,M.
Teixeira,S.R.
Muglia,V.F.
Vieira-Neto,O.M.
Dantas,M.
author_role author
author2 Moysés Neto,M.
Teixeira,S.R.
Muglia,V.F.
Vieira-Neto,O.M.
Dantas,M.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Romão,E.A.
Moysés Neto,M.
Teixeira,S.R.
Muglia,V.F.
Vieira-Neto,O.M.
Dantas,M.
dc.subject.por.fl_str_mv Autosomal dominant polycystic kidney disease
Hepatic cyst
Intracranial aneurysm
Arachnoid cyst
End-stage renal disease
topic Autosomal dominant polycystic kidney disease
Hepatic cyst
Intracranial aneurysm
Arachnoid cyst
End-stage renal disease
description The objective of the present study was to determine the frequency of the most common clinical features in patients with autosomal dominant polycystic kidney disease in a sample of the Brazilian population. The medical records of 92 patients with autosomal dominant polycystic kidney disease attended during the period from 1985 to 2003 were reviewed. The following data were recorded: age at diagnosis, gender, associated clinical manifestations, occurrence of stroke, age at loss of renal function (beginning of dialysis), and presence of a family history. The involvement of abdominal viscera was investigated by ultrasonography. Intracranial alterations were prospectively investigated by magnetic resonance angiography in 42 asymptomatic patients, and complemented with digital subtraction arteriography when indicated. Mean age at diagnosis was 35.1 ± 14.9 years, and mean serum creatinine at referral was 2.4 ± 2.8 mg/dL. The most frequent clinical manifestations during the disease were arterial hypertension (63.3%), lumbar pain (55.4%), an abdominal mass (47.8%), and urinary infection (35.8%). Loss of renal function occurred in 27 patients (mean age: 45.4 ± 9.5 years). The liver was the second organ most frequently affected (39.1%). Stroke occurred in 7.6% of the patients. Asymptomatic intracranial aneurysm was detected in 3 patients and arachnoid cysts in 3 other patients. In conclusion, the most common clinical features were lumbar pain, arterial hypertension, abdominal mass, and urinary infection, and the most serious complications were chronic renal failure and stroke. Both intracranial aneurysms and arachnoid cysts occurred in asymptomatic patients at a frequency of 7.14%.
publishDate 2006
dc.date.none.fl_str_mv 2006-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2006000400014
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 10.1590/S0100-879X2006000400014
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dc.publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
publisher.none.fl_str_mv Associação Brasileira de Divulgação Científica
dc.source.none.fl_str_mv Brazilian Journal of Medical and Biological Research v.39 n.4 2006
reponame:Brazilian Journal of Medical and Biological Research
instname:Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
instname_str Associação Brasileira de Divulgação Científica (ABDC)
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reponame_str Brazilian Journal of Medical and Biological Research
collection Brazilian Journal of Medical and Biological Research
repository.name.fl_str_mv Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)
repository.mail.fl_str_mv bjournal@terra.com.br||bjournal@terra.com.br
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