Late diagnosis of an index case of SDH-related paraganglioma/pheochromocytoma syndrome.

نویسندگان

  • Myriam Sánchez-Pacheco Tardón
  • Sol Serrano Corredor
  • Ana Carrión
  • Montserrat Mauri
  • Ana Yuste
چکیده

9. Arem R, Garber AJ, Field JB. Sulfonamide-induced hypoglycemia in chronic renal failure. Arch Intern Med. 1983;143:827--9. 10. Hughes CA, Chik CL, Taylor GD. Cotrimoxazole-induced hypoglycemia in an HIV-infected patient. Can J Infect Dis. 2001;12:314--6. 11. Shattner A, Rimon E, Green L, Coslovsky R, Bentwich Z. Hypoglycaemia induced by co-trimoxazole in AIDS. BMJ. 1988;297: 740. Juan Caro , Inmaculada Navarro-Hidalgo, Miguel Civera, José T. Real, Juan F. Ascaso

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منابع مشابه

Late diagnosis of an index case of SDH-related paraganglioma/ pheochromocytoma syndrome

9. Arem R, Garber AJ, Field JB. Sulfonamide-induced hypoglycemia in chronic renal failure. Arch Intern Med. 1983;143:827--9. 10. Hughes CA, Chik CL, Taylor GD. Cotrimoxazole-induced hypoglycemia in an HIV-infected patient. Can J Infect Dis. 2001;12:314--6. 11. Shattner A, Rimon E, Green L, Coslovsky R, Bentwich Z. Hypoglycaemia induced by co-trimoxazole in AIDS. BMJ. 1988;297: 740. Juan Caro , ...

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Pheochromocytoma in a Twelve-Year-Old Girl with SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

A twelve-year-old girl presented with a history of several weeks of worsening headaches accompanied by flushing and diaphoresis. The discovery of markedly elevated blood pressure and tachycardia led the child's pediatrician to consider the diagnosis of a catecholamine-secreting tumor, and an abdominal CT scan confirmed the presence of a pheochromocytoma. The patient was found to have a mutation...

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Clinicoradiological manifestations of paraganglioma syndromes associated with succinyl dehydrogenase enzyme mutation

BACKGROUND: Paragangliomas are rare tumours derived from the autonomic nervous system that have increasingly been recognised to have a genetic predisposition. Mutations of the enzyme succinyl dehydrogenase (SDH) have proven to result in paraganglioma formation. There are four subunits (A through D) that form the enzyme complex and are associated with different genophenotypic expressions of dise...

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15 YEARS OF PARAGANGLIOMA: Genetics and mechanism of pheochromocytoma-paraganglioma syndromes characterized by germline SDHB and SDHD mutations.

Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine neoplasms that derive from small paraganglionic tissues which are located from skull base to the pelvic floor. Genetic predisposition plays an important role in development of PPGLs. Since the discovery of first mutations in the succinate dehydrogenase D (SDHD) gene, which encodes the smallest subunit of mitochondrial complex I...

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Intrapericardial paraganglioma associated with succinate dehydrogenase complex subunit C mutation syndrome.

BACKGROUND Paragangliomas are benign neoplasms of neuroendocrine origin. It is estimated that from 20% to 50% of these tumors are familial. Mutations in the succinate dehydrogenase (SDH) gene family have been found to be responsible for a significant percentage of familial paragangliomas. METHODS A 33-year-old man who was found to have 3 synchronous primary tumors including a catecholamine-se...

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عنوان ژورنال:
  • Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion

دوره 59 2  شماره 

صفحات  -

تاریخ انتشار 2012