نتایج جستجو برای: secreting neoplasia

تعداد نتایج: 45603  

Journal: :Endocrine-related cancer 2012
R van der Pas W W de Herder L J Hofland R A Feelders

Cushing's syndrome (CS) is a severe endocrine disorder characterized by chronic cortisol excess due to an ACTH-secreting pituitary adenoma, ectopic ACTH production, or a cortisol-producing adrenal neoplasia. Regardless of the underlying cause, untreated CS is associated with considerable morbidity and mortality. Surgery is the primary therapy for all causes of CS, but surgical failure and ineli...

2017
Jason C. Mills James R. Goldenring

The development of intestinal-type gastric cancer is preceded by loss of parietal cells (oxyntic atrophy) and the induction of metaplastic cell lineages in the gastric mucosa. For example, mouse models have shown that spasmolytic polypeptide-expressing metaplasia can develop following oxyntic atrophy through transdifferentiation of zymogen-secreting chief cells. Evolution of spasmolytic polypep...

Journal: :The Medical journal of Malaysia 2006
A G Rohana M K Norazmi M Norlaila

Pheochromocytoma is a rare catecholamine-secreting tumour typically arising within the adrenal medulla. It may occur sporadically or be associated as part of a tumour syndrome including Von Hippel Lindau (VHL), Multiple Endocrine Neoplasia (MEN) 2 and Neurofibromatosis Type 1. VHL is associated with multi-organ involvement of benign and malignant tumours characterized by the presence of retinal...

Journal: :Archives of Iranian medicine 2014
Shiva Borzouei Seyed Habib Allah Mousavi Bahar Mohammad Amin Fereydouni Seyed Ahmadreza Salimbahrami Mehrdad Taghipour

Multiple Endocrine Neoplasia type IIa (MEN IIa) is an autosomal dominant syndrome characterized by pheochromocytoma, medullary thyroid carcinoma and hyperparathyroidism. Pheochromocytoma occurs in approximately 50% of patients with MEN IIa. This tumor has the capacity to produce ACTH ectopically and manifests as the Cushing syndrome, although it is very rare. We report a 26-year-old woman patie...

2012
H.S. Lee J.H. Chang S.K. Ku

The regional distribution and quantitative frequency of pancreatic endocrine cells were demonstrated in the Korean golden frog (Rana plancyi chosenica Okada), which is known as a Korean endemic species, for the first time, by immunohistochemical methods using specific mammalian antisera to insulin, glucagon, somatostatin and human pancreatic polypeptide (PP). In the pancreas of the Korean golde...

Journal: :international journal of molecular and clinical microbiology 0
nafise sadat naghavi department of microbiology, falavarjan branch, islamic azad university, isfahan, iran.سازمان اصلی تایید شده: دانشگاه آزاد اسلامی فلاورجان (islamic azad university of felavarjan) b mazrouei young researchers and elite club , falavarjan branch , islamic azad university , isfahan , iran.سازمان اصلی تایید شده: دانشگاه آزاد اسلامی فلاورجان (islamic azad university of felavarjan) m shanehsazzadeh zistpartac research institute, isfahan, iran es naghavi amin hospital, isfahan university of medical sciencesسازمان اصلی تایید شده: دانشگاه علوم پزشکی اصفهان (isfahan university of medical sciences)

the rate of cervical cancer in asians is deferent, based on the risk factors affecting and the rate of papiloma virus infection among females. cervical cancer is one of the important cancers between iranian women. in the present study the rate of cervical neoplasia was detected in isfahan and some risk factors affecting the incidence of cervical cancer was analyzed. the human papiloma virus inf...

B Mazrouei ES Naghavi M Shanehsazzadeh Nafise sadat Naghavi,

The rate of cervical cancer in Asians is deferent, based on the risk factors affecting and the rate of papiloma virus infection among females. Cervical cancer is one of the important cancers between Iranian women. In the present study the rate of cervical neoplasia was detected in Isfahan and some risk factors affecting the incidence of cervical cancer was analyzed. The human papiloma virus inf...

Journal: :international journal of endocrinology and metabolism 0
santosh kumar gupta department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]; department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected] suhas singla department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected] nishikant a damle department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected] krishankant agarwal department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected] chandersekhar bal department of nuclear medicine, all india institute of medical sciences, india +91-1126593530, [email protected]

abstract men-i is a rare genetic disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary gland, and pancreatic islet cells. we present a case of men-i syndrome diagnosed using predominantly nuclear medicine imaging followed by radionuclide therapy, thus emphasizing the role of nuclear imaging in diagnosing and treating men-i.

Journal: :the journal of tehran university heart center 0
sinan sabit-kocabeyoğlu yüksek i̇htisas cardiovascular education and research hospital, ankara, turkey. arda özyüksel department of cardiovascular surgery, medipol university, istanbul, turkey. erdem çetin department of cardiovascular surgery, memorial hospital, diyarbakır, turkey.

carney syndrome (cs) is an autosomal dominant multiple neoplasia syndrome that includes cardiac, endocrine, cutaneous, and neural tumors. cardiac myxomas can be seen in the course of cs. a 46-year-old female patient was admitted to our clinic with palpitation, cough, and exertional dyspnea. physical examination revealed pigmented lesions, especially scattered in the neck, chest, and extremities...

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