نتایج جستجو برای: adrenal tumor

تعداد نتایج: 477659  

ژورنال: :thrita 0
mohammad mozafar department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran mohammad reza radpey department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran niki tadayon department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran khashyar atqiaee department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran saran lotfollahzadeh department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran mohammad reza sobhiyeh department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran; department of general and vascular surgery, shohadaye tajrish medical center, shahid beheshti university of medical sciences, tehran, ir iran. tel/fax: +98-2122721144

conclusions this study provided clinico-epidemiological data on patients with cbt, which could be useful for prompt diagnosis and appropriate work-up for patients and families with cbts. results overall, 48 patients with 51 cbts were included in the study. the cbts were bilateral in 3 (6.25%) cases. the cardinal presentations of these cervical masses were unanimous in all patients; 6 (12.5%) ha...

Journal: :acta medica iranica 0
m razzaghy-azar a nickavar

pheochromocytomas are cathecolamine producing tumor arising from chromaffin cells of adrenal medulla and extra adrenal tissues. this is a report of a boy presented with headache and hypertension. in radiologic exams, an adrenal mass detected in the left side, with no renal tissue on that side. it was reported an adrenal pheochromocytoma in histopathology. renal agenesis confirmed during surgery...

Journal: :acta medica iranica 0
iraj nazari department of vascular surgery, sina trauma and surgery research center, sina hospital, tehran university of medical sciences, tehran, iran. fatemeh aarabi moghaddam research center, school of medicine, tehran university of medical sciences, tehran, iran. mohammad mahdi zamani research center, school of medicine, tehran university of medical sciences, tehran, iran. javad salimi department of vascular surgery, sina trauma and surgery research center, sina hospital, tehran university of medical sciences, tehran, iran.

carotid body tumors (cbts) are rare, slow-growing tumors that should be considered in evaluating every lateral neck mass. this single center study was performed to define demographic features, clinical characteristics and remedies of iranian patients with cbt. a retrospective review of prospectively collected data was done on 45 patients with 50 cbts who have been referred to sina hospital, teh...

دولتی, ماندانا, مهرآزما, میترا,

    Background: Adrenal cortical carcinoma is a rare malignant tumor which presents mainly in late adulthood with an equal age distribution. The tumor is usually functionally active. Case report: The present study reports two 11-month-old female infants with abdominal mass and virilysm who underwent radical nephrectomy. The final diagnosis was adrenal cortical carcinoma with regional lymph node...

Journal: :iranian journal of pediatric hematology and oncology 0
zahra razavi associated professor, pediatric endocrinologist, pediatrics department, besat hospital, hamedan university of medical scسازمان های دیگر: assistant professor pathology department, besat hospital,,hamedan university of medical sciences, hamadan, iran alireza rastgoohaghi assistant professor pathology department, besat hospital,,hamedan university of medical sciences, hamadan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی همدان (hamadan university of medical sciences)

adrenocortical tumors (acts) are extremely rare in infants. pediatric acts are therapeutic and diagnostic challenge because histological criteria for distinguishing benign from malignant tumors seen in adults are not always reliable in children .the aim of this report was to present clinical features, hormonal profile, and histopathological characteristics of an infant with adrenal tumors. a 10...

Ali Hadipour, Elham Jafari, Hamid Pakmanesh, Najmeh sadat Fadaei

Adrenal myelolipoma is a rare benign tumor that is composed of hematopoietic cells and mature fat. Mostly, these nonfunctioning tumors are distinguished incidentally during autopsy or radiologic investigations. Here, we report a case of 46-year-old man presented with nonspecific abdominal pain for one year, who had right adrenal mass with fat density detected by radiologic investigation. Histop...

Journal: :nephro-urology monthly 0
bita geramizadeh department of pathology, shiraz university of medical sciences, shiraz, ir iran; transplant research center, shiraz university of medical sciences, shiraz, ir iran; department of pathology, medical school, shiraz university of medical sciences, shiraz, ir iran. tel/fax: +98-7136473238 shahrzad yazdanpanah department of pathology, shiraz university of medical sciences, shiraz, ir iran heshmatollah salahi department of surgery and transplant, shiraz university of medical sciences, shiraz, ir iran mahsa marzban transplant research center, shiraz university of medical sciences, shiraz, ir iran

conclusions in evaluation of adrenal masses cystic lymphangioma should be considered as a differential diagnosis. introduction adrenal cystic lymphangioma is a rare benign tumor, which is nearly always asymptomatic and incidentally discovered during routine imaging work-ups or investigating other pathologies. case report a 43-year-old female presented hypertension, which during routine work-up ...

Journal: :nephro-urology monthly 0
santosh kumar department of urology, post graduate institute of medical education and research, chandigarh, india; department of urology, post graduate institute of medical education and research, chandigarh, india. tel: +91-941737406, fax: +91-1722744401 kumar jayant department of urology, post graduate institute of medical education and research, chandigarh, india seema prasad department of urology, post graduate institute of medical education and research, chandigarh, india swati agrawal department of obstetrics and gynaecology, post graduate institute of medical education and research, chandigarh, india kalpesh mahesh parmar department of urology, post graduate institute of medical education and research, chandigarh, india rajesh roat department of urology, post graduate institute of medical education and research, chandigarh, india

introduction adrenal myelolipoma is a rare benign neoplasm, which contains mature adipose tissue and variable amounts of haematopoietic elements. most lesions are small and asymptomatic, discovered incidentally during autopsy or imaging studies performed for other reasons. case presentation here we reported a series of two cases of giant myelolipomas of the adrenal gland; first one the largest ...

Bazrafshan, Behnaz, Fazel, Abdolreza, Hashempour, Mohammad Reza, Jouybari, Leila, Rostami, Masoomeh, Sanagoo, Akram, Sarmadi, Payam, Shirangi, Seyed Payam,

Abstract Adrenal gland cysts are rare indications of adrenal diseases, which are commonly asymptomatic. In radiological studies, these cysts, known as incidentalomas, are often detected by coincidence accounting for 6% of the population. Adrenal incidentalomas are commonly detected, and autonomous cortisol hypersecretion is the most prevalent abnormality associated with these masses. Since thi...

Journal: :iranian journal of radiology 0
bushra johari department of biomedical imaging, university malaya of research imaging center, faculty of medicine, university malaya, kuala lumpur, malaysia; faculty of medicine, university teknologi mara, jalan hospital, sungai buloh selangor, malaysia; faculty of medicine, mara university of technology, jalan hospital, sungai buloh selangor, malaysia. tel: +6012-3729495 yang faridah abdul aziz department of biomedical imaging, university malaya of research imaging center, faculty of medicine, university malaya, kuala lumpur, malaysia sivakumar krishnasamy department of surgery, university of malaya medical center, kuala lumpur, malaysia lai meng looi department of pathology, university of malaya medical center, kuala lumpur, malaysia shahrul amry hashim department of surgery, university of malaya medical center, kuala lumpur, malaysia raja amin raja mokhtar department of surgery, university of malaya medical center, kuala lumpur, malaysia

the presence of tumor thrombus in the right atrium is frequently the result of direct intraluminal extension of infra-diaphragmatic malignancy into the inferior vena cava (ivc) or supradiaphragmatic carcinoma into the superior vena cava (svc). right atrial tumor thrombus with extension into both svc and ivc has not been reported in the literature. we present a patient who presented with symptom...

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