Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico

Familial hyperparathyroidism can be a part of a type 1 or 2 multiple endocrine neoplasia syndrome, can be associated to mandibular fibromas or can appear as an isolated disease. We report a family with 11 members affected by a primary hyperparathyroidism, all with a history of kidney stones and with...

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Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2001
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001001100011
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spelling oai:scielo:S0034-988720010011000112002-06-12Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico Hyperparathyroidism Multiple endocrine neoplasia syndrome Pedigree Familial hyperparathyroidism can be a part of a type 1 or 2 multiple endocrine neoplasia syndrome, can be associated to mandibular fibromas or can appear as an isolated disease. We report a family with 11 members affected by a primary hyperparathyroidism, all with a history of kidney stones and without evidences of other endocrine tumors. Not knowing the familial history of the disease, only one adenoma was resected in four cases and in all, the disease recidivated. Two were operated again, performing a total parathyroidectomy and heterologous autotransplantation of parathyroid tissue in the forearm. The presentation form of primary hyperparathyroidism in this family, is similar to other reported cases. It is more aggressive, is diagnosed at a lower age, has a higher incidence of recurrence and multiglandular involvement than the sporadic disease. (Rev Méd Chile 2001; 129: 1311-4)info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.129 n.11 20012001-11-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001001100011es10.4067/S0034-98872001001100011
institution Scielo Chile
collection Scielo Chile
language Spanish / Castilian
topic Hyperparathyroidism
Multiple endocrine neoplasia syndrome
Pedigree
spellingShingle Hyperparathyroidism
Multiple endocrine neoplasia syndrome
Pedigree
Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico
description Familial hyperparathyroidism can be a part of a type 1 or 2 multiple endocrine neoplasia syndrome, can be associated to mandibular fibromas or can appear as an isolated disease. We report a family with 11 members affected by a primary hyperparathyroidism, all with a history of kidney stones and without evidences of other endocrine tumors. Not knowing the familial history of the disease, only one adenoma was resected in four cases and in all, the disease recidivated. Two were operated again, performing a total parathyroidectomy and heterologous autotransplantation of parathyroid tissue in the forearm. The presentation form of primary hyperparathyroidism in this family, is similar to other reported cases. It is more aggressive, is diagnosed at a lower age, has a higher incidence of recurrence and multiglandular involvement than the sporadic disease. (Rev Méd Chile 2001; 129: 1311-4)
title Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico
title_short Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico
title_full Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico
title_fullStr Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico
title_full_unstemmed Hiperparatiroidismo primario, aislado y de carácter familiar: Caso clínico
title_sort hiperparatiroidismo primario, aislado y de carácter familiar: caso clínico
publisher Sociedad Médica de Santiago
publishDate 2001
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872001001100011
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