نتایج جستجو برای: adrenal

تعداد نتایج: 54479  

Journal: :international journal of endocrinology and metabolism 0
gul bano farheen mir department of paediatrics, watford general hospital, uk nigel beharry department of radiology, st. george's health nhs trust, uk philip wilson department of cellular pathology, st. george's healthcare nhs trust, uk shirley hodgson clinical developmental sciences, st george’s university of london, uk stephen schey department of haematology, kings college london, se5 9rs, uk

a 64-year-old male presented with neurofibromatosis 1 and cushing’s syndrome. clinically he was over weight, depressed with extensive skin bruising and hypertension. his 24 hours urinary metanephrines, urinary 5hiaa, gut peptides and chromgranin levels were normal. his renal function and renal mri scan was also normal. his cortisol failed to suppress on overnight dexamethsone suppression test. ...

Adrenal lesions are commonly observed during 18F-FDG PET/CT studies. Although, most of these lesions are considered benign, an important consideration in oncologic patients is metastasis. Benign lesions, such as adenomas usually present with low 18F-FDG uptake, although overlap with malignant lesions exist and clear SUV cut-off for distinguishing adrenal adenomas has not b...

Journal: :international journal of endocrinology and metabolism 0
nasiroglu narin imga ankara numune education and research hospital, department of endocrinology, ankara, turkey; ankara numune education and research hospital, department of endocrinology, ankara, turkey. tel: +90-5056492934, fax: +90-3124263838 ozgul ucar elalmis ankara numune education and research hospital, department of cardiology, ankara, turkey mazhar muslum tuna ankara numune education and research hospital, department of endocrinology, ankara, turkey bercem aycıcek dogan ankara numune education and research hospital, department of endocrinology, ankara, turkey deniz sahin ankara numune education and research hospital, department of cardiology, ankara, turkey dilek berker ankara numune education and research hospital, department of endocrinology, ankara, turkey

conclusions in this study we showed that eft, measured by echocardiography is higher in subjects with ai when compared to healthy controls. epicardial fat thickness had the best independent correlation with ai in multiple logistic regression analysis. incidentaloma is also associated with increased left ventricular mass index and cimt. adrenal incidentaloma patients may show early cardiac chang...

Journal: :acta medica iranica 0
sedighe moradi institue of endocrinology and metabolism, iran university of medical sciences, tehran, iran. mohammadreza shafiepour rafsanjan university of medical sciences, rafsanjan, iran. alireza amirbaigloo institue of endocrinology and metabolism, iran university of medical sciences, tehran, iran.

normotensive hyperaldosteronism is a rare disorder. it is usually diagnosed with hypokalemia or an adrenal mass. our patient was a 27-year-old female presented with weakness. she had normal blood pressure, hypokalemia, high plasma aldosterone level and suppressed plasma renin activity. after the saline load, test aldosterone didn’t show suppression. adrenal computed tomography revealed a left a...

Didem Atici Emel Ünsür Ismail Dursun Mehmet Sait Doğan Ruhan Düşünsel Sibel Yel

Background: Adrenal hematoma is a very rare acquired cause of neonatal hypertension. In this study, we report a case of neonatal hypertension associated with adrenal hematoma. A male neonate was immediately transferred to our neonatal intensive care unit after delivery due to meconium aspiration. He needed to be on mechanical ventilation support. During his hospital stay, hospital records showe...

Journal: :گوارش 0
ahmad khodadad mehri najafi-sani fatemeh famouri v modaresi

allgrove syndrome also known as triple-a syndrome is an autosomal recessive disorder characterized by alacremia, achalasia and acth-resistant adrenal insufficiency. although this syndrome is rare, herein we report four cases with different clinical manifestations. they were referred to the gastrointestinal ward during a one year period with complaints of vomiting and dysphagia. the diagnosis of...

روحانی, فرزانه , گریگوریان, آرتین ,

    Background & Objective: Congenital Adrenal Hyperplasia(CAH) includes a group of inherited diseases which are caused by enzyme defects in the synthesis of cortisol from cholesterol. It manifests itself in different forms like ambiguous genitalia, adrenal crisis in infants, precocious puberty in children, hirsutism, oligomenorrhea and infertility in adults. Although CAH is one of the most com...

بهرامیان, بیتا , هورمزدی, مهشید ,

In this case report, we present a 40-year-old man with the history of flank pain and weight loss in recent months. A left adrenal mass was the sonographic finding supported by CT-Scan. After light microscopic and immunohistochemistry examination and based on “ pheochromocytoma of adrenal gland scaled score(PASS)” the diagnosis was “Histologic malignant pheochromocytoma”. ...

A. Bahoddini G.A. Dehghani M. Monsefi, S. Nazemi

Background: Noise pollution is considered as a stressful factor in every day’s life of the industrial world. The present study was designed to investigate the probable effects of different time exposure of noise stress on histomorphometric changes of adrenal gland, plasma cortisol and body weight of the rat. Methods: Sixty adult male Wistar rats were divided into two series of short time noise ...

حشمت مویری, ,

The development of testicular masses in male patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency has been recognized for many years. We present here the eighth and ninth reported patient with bilateral testicular tumors associated with 11 hydroxylase deficiency. They were two brothers aged 7.5 and 5 yr. who had bilateral testicular tumors and diagnosed because of signs...

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