نتایج جستجو برای: adrenal mass

تعداد نتایج: 527921  

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”. ...

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...

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: :journal of nursing and midwifery sciences 0
behnaz bazrafshan medical cellular and molecular research center, golestan university of medical sciences, gorgan, iran payam sarmadi family medicine department, faculty of medicine, isfahan university of medical sciences, isfahan, iran mohammad reza hashempour students research committee, department of surgery, 5-azar teaching hospital, golestan university of medical sciences, gorgan, iran masoomeh rostami department of parasitology and mycology, school of medicine, golestan university of medical sciences, gorgan, iran abdolreza fazel department of surgery, 5-azar teaching hospital, golestan university of medical sciences, gorgan, iran akram sanagoo nursing research center, department of nursing, golestan university of medical sciences, gorgan, iran

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 this...

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...

Jin Lin Ling Zhang Lu Ding Ping Li, Ping-Ping Qiu Wei-Wu Liu Xue-Mei He Yan-Kun Sha Yan-Wei Sha Yue-Qiang Song

21-hydroxylase deficiency (21-OHD) caused congenital adrenal hyperplasia (CAH) is a group of autosomal recessive genetic disorders resulting from mutations in genes involved with cortisol (CO) synthesis in the adrenal glands. Testicular adrenal rest tumors (TARTs) are rarely the presenting symptoms of CAH. Here, we describe a case of simple virilizing CAH with TARTs, in a 15-year-old boy. The p...

Journal: :Case Reports 2011

Journal: :international journal of fertility and sterility 0
yan-kun sha yan-wei sha lu ding wei-wu liu yue-qiang song jin lin

21-hydroxylase deficiency (21-ohd) caused congenital adrenal hyperplasia (cah) is a group of autosomal recessive genetic disorders resulting from mutations in genes involved with cortisol (co) synthesis in the adrenal glands. testicular adrenal rest tumors (tarts) are rarely the presenting symptoms of cah. here, we describe a case of simple virilizing cah with tarts, in a 15-year-old boy. the p...

Journal: :Indian Journal of Endocrinology and Metabolism 2012

Journal: :The Journal of the Association of Physicians of India 2006
M Kulkarni Shashank R Joshi

A 65 yrs old male patient and a known case of carcinoma of prostate with finding of a small adrenal mass on CT scan. MRI is done to rule out metastasis of adrenal. On in-phase and out phase imaging (Figs. 1,2) showing a significant loss of signals within the mass on out of phase imaging suggestive of lipid rich adrenal adenoma. The signal intensity drops below signals of spleen. Fig. 1 : In pha...

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