نتایج جستجو برای: parathyroid hyperplasia

تعداد نتایج: 49719  

Journal: :Journal of the American Society of Nephrology : JASN 2000
A Canalejo Y Almadén V Torregrosa J C Gomez-Villamandos B Ramos J M Campistol A J Felsenfeld M Rodríguez

Calcitriol treatment is used to reduce parathyroid hormone levels in azotemic patients with secondary hyperparathyroidism (HPT). Whether long-term calcitriol administration reduces parathyroid gland size in patients with severe secondary hyperparathyroidism is not clear. The aim of the study was to evaluate in vitro the effect of calcitriol on parathyroid cell proliferation and apoptosis in nor...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2003
Nobuo Nagano Sonoe Miyata Sachiko Obana Nami Kobayashi Megumi Abe Naoshi Fukushima Michihito Wada

BACKGROUND Secondary hyperparathyroidism characterized by hyperplasia of the parathyroid gland (PTG) is a consequence of chronic renal insufficiency (CRI). Dietary phosphate restriction and sevelamer hydrochloride, a calcium-free phosphate binder, suppress parathyroid hormone (PTH) secretion and PTG hyperplasia in experimental animals with CRI, independently of serum calcium and 1,25(OH)(2)D(3)...

Journal: :Arquivos de neuro-psiquiatria 2005
Alzira Alves Siqueira Carvalho Adriano Vieira Hougelle Simplício Satomi Fugygara Solyon Maia Carvalho Moacyr Pezati Rigueiro

We report a case of a 26-year-old man who presented a lower motor neuron syndrome due to hyperparathyroidism. Electromyography showed neurogenic features with normal nerve conduction studies. Hypercalcemia led to the discovery of a primary hyperparathyroidism with gland hyperplasia. Following parathyroid surgery there was recovery of the neurological symptoms.

2016
E.A. Soler Arias V.A. Castillo R.H. Trigo M.E. Caneda Aristarain

Human multiple endocrine neoplasia subtype 2A (MEN 2A) is characterized by medullary thyroid carcinoma, pheochromocytoma and parathyroid hyperplasia or adenoma in the same individual. In this report, a case of a female Rottweiler with medullary thyroid carcinoma, bilateral pheochromocytoma and parathyroid adenoma was described. Clinical manifestations of muscle weakness, polydipsia, polyuria, d...

2008
Noritaka Onoda Masafumi Fukagawa Yoshihiro Tominaga Masafumi Kitaoka Tadao Akizawa Fumihiko Koiwa Takatoshi Kakuta Kiyoshi Kurokawa

In 2000, the Japanese Society for Parathyroid Intervention issued the 'Guidelines for percutaneous ethanol injection therapy of the parathyroid glands in chronic dialysis patients'. Since then, the concept of 'selective PEIT' has been well accepted and the number of patients treated by this method in Japan has increased. Recently, it has been reported that the effect of PEIT differs depending o...

Journal: :Hormones 2002
Helen Thomopoulou

In 1920, F.A. entered Harvard Medical School, and graduated in 1924. He then worked as an intern at the Massachusetts General Hospital (M.G.H.) in the Department of Dr. J. Aub and W. Bauer where he was initiated into the field of the parathyroid glands and calcium metabolism. In 1927 and 1928, at Johns Hopkins Hospital in Baltimore, Albright together with Dr. R. Ellsworth studied and published ...

2012
You Lim Kim Young Woo Jang Jin Taek Kim Su Ah Sung Tae Seok Lee Won Mi Lee Hyo Jeong Kim

Multiple endocrine neoplasia type 1 (MEN1) syndrome includes varying combinations of endocrine and non-endocrine tumors. There are also a considerable number of atypical MEN1 syndrome. In this case, a 68-yr-old woman was referred to the Department of Endocrinology for hypercalcemia. Five years ago, she had diagnosed as primary hyperaldosteronism and now newly diagnosed as parathyroid hyperplasi...

Journal: :Head & neck 2015
Oliwia Anna Segiet Mariusz Deska Marek Michalski Jacek Gawrychowski Romuald Wojnicz

BACKGROUND Primary hyperparathyroidism (HPT) is one of the most common endocrine disorders, defined by hypersecretion of parathormone. Primary HPT can be caused by adenoma, hyperplasia, and carcinoma. A great amount of mechanisms contribute to the pathogenesis of this disease, such as genetic predispositions because of the germline-inactivating mutations in the multiple endocrine neoplasia type...

Journal: :The Journal of clinical endocrinology and metabolism 1992
S A Rivkees G el-Hajj-Fuleihan E M Brown J D Crawford

We report the development of severe tertiary hyperparathyroidism in three girls treated for familial hypophosphatemic rickets and characterize parathyroid function in vivo and in vitro. All patients had been previously treated with relatively large doses of inorganic phosphorus (125 mm/day) and ergocalciferol or calcitriol for several years and had radiographic evidence of long-standing hyperpa...

Journal: :The Keio journal of medicine 1971
S Furuya S Baba

Cysts which originated from embryonal remnants are often observed in the cervical region. Among these cysts, branchiogenic cleft cysts and thyroglossal cysts are most commonly encountered. Parathyroid cysts and cervical thymic cysts are known to be a rare entity. Reviewing the world literature of the latter two, only a few reports were noted. There is, in addition, some confusion in terminology...

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