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1.
Medicine (Baltimore) ; 95(20): e3683, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-27196476

RESUMO

Osteoporosis and osteoporotic fractures represent a substantial health burden, and predominantly affect the elderly. Younger generations may also develop these conditions because of various predisposing conditions, including primary hyperparathyroidism. However, little information is available regarding early skeletal manifestations of primary hyperparathyroidism.A 30-year-old Japanese male presented with pain in his left wrist, and was diagnosed with a distal radius fracture. During surgery, we noticed decreased bone strength of the fracture site. Further investigation found osteoporosis and primary hyperparathyroidism owing to a solitary parathyroid adenoma, which was resected without significant complications. History revealed that the patient suffered a metacarpal bone fracture of his right fifth bone 6 months earlier. Although serial x-rays at that time had shown rapidly developed cortical bone erosion around the fractured finger, the possibility of primary hyperparathyroidism was overlooked because of poor awareness of the condition, leading to a 6-month delay in the diagnosis of primary hyperparathyroidism.Clinicians should be aware that finger fractures may be an early skeletal manifestation of primary hyperparathyroidism that can help achieve a prompt diagnosis of the condition, especially when they occur in young adults in the absence of major trauma.


Assuntos
Adenoma/complicações , Hiperparatireoidismo Primário/etiologia , Ossos Metacarpais/lesões , Osteoporose/etiologia , Fraturas por Osteoporose/etiologia , Neoplasias das Paratireoides/complicações , Absorciometria de Fóton , Adenoma/diagnóstico por imagem , Adulto , Humanos , Masculino , Ossos Metacarpais/diagnóstico por imagem , Osteoporose/diagnóstico por imagem , Fraturas por Osteoporose/diagnóstico por imagem , Neoplasias das Paratireoides/diagnóstico por imagem , Cintilografia , Fraturas do Rádio/diagnóstico por imagem , Fraturas do Rádio/etiologia , Recidiva , Tomografia Computadorizada por Raios X
2.
J Pediatr Orthop B ; 25(1): 48-53, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26288374

RESUMO

Gorham's disease (GD) is a rare and intractable disease characterized by marked progression of osteolysis associated with lymphangioma and/or hemangioma. Here, we describe a case of GD of the proximal tibia occurring in a 10-year-old boy. Although we could not correctly diagnose it at first, we finally diagnosed him as having GD. Progression of osteolysis of the tibia stopped 3 months after the local administration of OK-432. Thereafter, the huge bone defect with varus and extension deformity was reconstructed successfully by distraction osteogenesis using the Ilizarov method. The present case suggests that local administration of OK-432, followed by distraction osteogenesis is a treatment option for GD.


Assuntos
Antineoplásicos/uso terapêutico , Osteogênese por Distração/métodos , Osteólise Essencial/terapia , Picibanil/uso terapêutico , Tíbia/cirurgia , Criança , Humanos , Masculino , Resultado do Tratamento
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