Pheochromocytoma and Clear-Cell Renal Carcinoma in a Child with von Hippel-Lindau Disease: A Patient Report

Autor:	Rituerto B, Alonso F, Caimari M, Ferragut J, Herrera M, Gómez-Rivas B
Rok vydání:	1999
Předmět:	Adult Male Pathology medicine.medical_specialty von Hippel-Lindau Disease endocrine system diseases Ubiquitin-Protein Ligases Endocrinology Diabetes and Metabolism Adrenal Gland Neoplasms Pheochromocytoma Disease urologic and male genital diseases Ligases Catecholamines Endocrinology medicine Humans Von Hippel–Lindau disease Child Carcinoma Renal Cell neoplasms business.industry Tumor Suppressor Proteins Proteins medicine.disease Kidney Neoplasms female genital diseases and pregnancy complications nervous system Von Hippel-Lindau Tumor Suppressor Protein Hypertension Mutation Pediatrics Perinatology and Child Health Clear Cell Renal Carcinoma Female Cerebellar hemangioblastoma Presentation (obstetrics) Patient report business Renal carcinoma
Zdroj:	Journal of Pediatric Endocrinology and Metabolism. 12
ISSN:	2191-0251 0334-018X
DOI:	10.1515/jpem.1999.12.4.579
Popis:	A 6 year-old boy with von Hippel-Lindau (VHL) disease presented with hypertension due to bilateral pheochromocytomas. At age 13 he developed a renal carcinoma and bilateral paragangliomas. His mother had retinal angiomas, bilateral pheochromocytomas and a cerebellar hemangioblastoma. This unusual presentation illustrates the complexity and difficulties associated with the management of VHL disease.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd16d2d0d5a4cbad3f162d287f9df3eb https://doi.org/10.1515/jpem.1999.12.4.579 Zobrazit plný text záznamu