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Brown Tumor of the Humerus Associated with Secondary Hyperparathyroidism: A Case Report of Successful Treatment after Subtotal Parathyroidectomy / 대한내분비외과학회지
Korean Journal of Endocrine Surgery ; : 92-95, 2013.
Artigo em Coreano | WPRIM | ID: wpr-39200
ABSTRACT
Brown tumor is a bone disease that arises in the setting of increased osteoclastic activity and fibroblastic proliferation in the involved bone. It is well recognized as serious complication of hyperparathyroidism. Brown tumor is uncommon, and brown tumor with secondary hyperparathyroidism resulting from chronic renal failure has rarely been reported. We recently experienced a case of a 28-year-old Korean woman with chronic renal failure caused by chronic glomerulonephritis, on hemodialysis for nine years. She has been hospitalized with left shoulder pain for two years. Image studies showed multiple cystic masses, and both suspicious marked thinning and partial destruction of the cortex on the head of the left humerus. Histopathologic analysis of the mass lesion showed a fibrotic capsule, hemosiderin pigmentation, and giant cell, all characteristic of brown tumor. A subtotal parathyroidectomy was done without surgery of the bony lesion (brown tumor), with successful results. We report this case with a brief review of the literature.
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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Osteoclastos / Doenças Ósseas / Pigmentação / Células Gigantes / Paratireoidectomia / Diálise Renal / Dor de Ombro / Fibroblastos / Glomerulonefrite / Cabeça Limite: Adulto / Feminino / Humanos Idioma: Coreano Revista: Korean Journal of Endocrine Surgery Ano de publicação: 2013 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Osteoclastos / Doenças Ósseas / Pigmentação / Células Gigantes / Paratireoidectomia / Diálise Renal / Dor de Ombro / Fibroblastos / Glomerulonefrite / Cabeça Limite: Adulto / Feminino / Humanos Idioma: Coreano Revista: Korean Journal of Endocrine Surgery Ano de publicação: 2013 Tipo de documento: Artigo