نتایج جستجو برای: adrenal adenoma

تعداد نتایج: 74473  

2016
Mehmet Fatih EKİCİ Murat SEYİT

Isolated adrenal gland adenoma hematomas are rare . We reported a case who was 45 yeras-old admitted to Emergency Service after a traffic accident and had an adrenal gland adenoma hematomas.

Journal: :American Journal of Surgical Pathology 2013

Journal: :World Journal of Surgical Oncology 2007
Izhar N Bagwan Gary Cook Satvinder Mudan Andrew Wotherspoon

BACKGROUND The most common tumours of the adrenal gland are adenoma, pheochromocytoma, adrenocortical carcinoma, and metastases. Although the imaging features of these tumours are established, the imaging characteristics of uncommon adrenal masses are less well known. In patients with extradrenal tumour, incidental discovery of an adrenal mass necessitates excluding the possibility of metastati...

2016
Samay Sappal Jay Sulek Steven C. Smith Lance J. Hampton

BACKGROUND We present an intrarenal adrenocortical adenoma discovered incidentally after robot-assisted partial nephrectomy and total adrenalectomy for a suspicious renal mass. Current literature describes the rare occurrence of an adrenocortical adenoma arising from a renal-adrenal fusion. This case represents an uncommon, benign pathology that should be considered in the differential diagnosi...

Journal: :AJR. American journal of roentgenology 1982
H S Glazer P J Weyman S S Sagel R G Levitt B L McClennan

Sixteen adrenal masses were identified with computed tomography (CT) in patients who had no clinical or biochemical evidence of adrenal pathology. In five patients, an adrenalectomy was performed, disclosing either an adenoma or nodular hyperplasia. Autopsy disclosed a cortical adenoma in one patient who died from unrelated causes. In the remaining 10 patients, follow-up scans 4--16 months late...

Journal: :European journal of endocrinology 2005
Ernesto De Menis Federico Roncaroli Vladimiro Calvari Valerio Chiarini Paolo Pauletto Giovanna Camerino Nadia Cremonini

OBJECTIVE Mutations in the DAX-1 gene result in X-linked congenital adrenal hypoplasia. The classic clinical presentation is primary adrenal insufficiency in early life and hypogonadotropic hypogonadism at the time of expected puberty, but recent data have expanded the phenotypic spectrum of DAX-1 mutations. We report the occurrence of an ACTH-secreting adenoma in a patient with X-linked congen...

Journal: :QJM : monthly journal of the Association of Physicians 1981
R Harper C G Ferrett J A McKnight E M McIlrath C F Russell B Sheridan A B Atkinson

In primary hyperaldosteronism, it is important to distinguish between unilateral and bilateral disease, as management strategies differ. In the period 1983-95, we identified 34 patients with primary hyperaldosteronism. Following further investigations, a diagnosis of aldosterone-secreting adenoma was made in 17 patients, and surgery was performed. Computed tomography clearly localized an appare...

Journal: :Internal medicine 2009
Takeshi Nigawara Satoru Sakihara Kazunori Kageyama Ken Terui Shinobu Takayasu Shingo Hatakeyama Chikara Ohyama Hironobu Sasano Toshihiro Suda

A 68-year-old woman was referred for characterization of a left adrenal incidentaloma. Endocrinological examinations indicated subclinical Cushing's syndrome, whereas the large volume (10 cm in diameter) and heterogeneous configuration of the tumor raised a strong suspicion of adrenal carcinoma. Hence, left adrenalectomy was performed. Histopathologically, this lesion was a thick hyaline-walled...

2014
Brian R Untch Jinru Shia Robert J Downey Jorge A Carrasquillo David M Panicek Vivian E Strong

OBJECTIVE We report a case of an adrenal collision tumor composed of a small cell lung carcinoma metastasis and a benign adrenal adenoma identified preoperatively on FDG-PET, CT and MRI and confirmed pathologically. METHODS The patient's history, preoperative imaging characteristics, postoperative course, and histopathology are described. A review of the literature addressing adrenal collisio...

Journal: :Endocrine Abstracts 2016

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