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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Sociedad Médica de Santiago
2001
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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 |
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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 |
_version_ |
1718436001237434368 |