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Adrenal Mass

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3661. Diagnosis of abdominal masses with percutaneous biopsy guided by ultrasound. (PubMed)

in a spring loaded firing device (Biopty gun) that was advanced under simultaneous ultrasound scanning, permitting precise localisation of the target organ.Results of histological examination of tissue specimens.Biopsy failed in four patients. Adequate histological specimens were obtained in 104 patients with masses in the liver (31), pancreas (37), kidney (10), and adrenal glands (six) and in 20 undiagnosed abdominal and retroperitoneal masses. Follow up was until death or confirmation of the diagnosis (...) Diagnosis of abdominal masses with percutaneous biopsy guided by ultrasound. To assess the accuracy and safety of percutaneous biopsy of abdominal masses guided by ultrasound.Prospective study.Combined gastroenterology service, Scarborough Hospital.108 Consecutive patients identified as having a discrete mass on diagnostic ultrasound examination of the abdomen.A sample of tissue was obtained with an aseptic technique under local anaesthesia: an 18 steel wire gauge needle (Tru-Cut) was mounted

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1990 BMJ : British Medical Journal

3662. 34-year-old woman with hypotension, respiratory failure, fever, and an abdominal mass. (PubMed)

34-year-old woman with hypotension, respiratory failure, fever, and an abdominal mass. 8342266 1993 08 31 2018 11 13 0093-0415 158 5 1993 May The Western journal of medicine West. J. Med. 34-year-old woman with hypotension, respiratory failure, fever, and an abdominal mass. 499-505 Lee P C PC Department of Medicine, Stanford University Medical Center, CA 94305. Gocke C D CD Harris E D ED Jr Pillsbury H E HE Bergin C J CJ Vosti K L KL Melmon K L KL Clinkingbeard C C eng Case Reports Clinical (...) Conference Journal Article United States West J Med 0410504 0093-0415 AIM IM Adrenal Gland Neoplasms diagnosis Adult Diagnosis, Differential Female Humans Pheochromocytoma diagnosis 1993 5 1 2001 3 28 10 1 1993 5 1 0 0 ppublish 8342266 PMC1022132 N Engl J Med. 1979 Sep 27;301(13):682-6 481462 Am J Surg Pathol. 1980 Apr;4(2):121-6 6103678 N Engl J Med. 1984 Nov 15;311(20):1298-303 6149463 Hum Pathol. 1985 Jun;16(6):580-9 3997135 Radiology. 1987 Oct;165(1):89-93 3628794 N Engl J Med. 1988 Jul 21;319(3):136

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1993 Western Journal of Medicine

3663. Adrenal mass evaluation in patients with lung carcinoma: a cost-effectiveness analysis

Adrenal mass evaluation in patients with lung carcinoma: a cost-effectiveness analysis Adrenal mass evaluation in patients with lung carcinoma: a cost-effectiveness analysis Adrenal mass evaluation in patients with lung carcinoma: a cost-effectiveness analysis Remer E M, Obuchowski N, Ellis J D, Rice T W, Adelstein D J, Baker M E Record Status This is a critical abstract of an economic evaluation that meets the criteria for inclusion on NHS EED. Each abstract contains a brief summary (...) of the methods, the results and conclusions followed by a detailed critical assessment on the reliability of the study and the conclusions drawn. Health technology Strategies for adrenal mass evaluation in patients with lung carcinoma. The following strategies were evaluated: (1) CT (0 H) followed by MR imaging followed by CT biopsy; (2) CT (10 H) followed by MR imaging followed by CT biopsy; (3) CT (0 H) followed by CT biopsy; (4) CT (10 H) followed by CT biopsy; (5) MR imaging followed by CT (0 H) followed

2000 NHS Economic Evaluation Database.

3664. Management of clinically inapparent adrenal mass

Management of clinically inapparent adrenal mass Management of clinically inapparent adrenal mass Management of clinically inapparent adrenal mass Lau J, Balk E, Rothberg M, Ioannidis J P A, DeVine D, Chew P, Kupelnik B, Miller K Record Status This is a bibliographic record of a published health technology assessment from a member of INAHTA. No evaluation of the quality of this assessment has been made for the HTA database. Citation Lau J, Balk E, Rothberg M, Ioannidis J P A, DeVine D, Chew P (...) , Kupelnik B, Miller K. Management of clinically inapparent adrenal mass. Rockville: Agency for Healthcare Research and Quality (AHRQ). Evidence Report/Technology Assessment No. 56. 2002 Authors' objectives This report aims to assess the available evidence on the management of clinically inapparent adrenal mass. The widespread use of computed tomography (CT), magnetic resonance imaging (MRI), and ultrasound imaging (US) has resulted in the incidental discovery of asymptomatic adrenal masses (also

2002 Health Technology Assessment (HTA) Database.

3665. Role of protein kinase C in the regulation of histamine and bradykinin stimulated inositol polyphosphate turnover in adrenal chromaffin cells. (PubMed)

Role of protein kinase C in the regulation of histamine and bradykinin stimulated inositol polyphosphate turnover in adrenal chromaffin cells. 1. The possibility that bradykinin- or histamine-stimulated inositol polyphosphate accumulation may be regulated by protein kinase C (PKC) in bovine adrenal chromaffin cells has been addressed. 2. Initial experiments confirmed that the phorbol ester 12-O-tetradecanoyl-phorbol 13-acetate (TPA) dramatically inhibited agonist-stimulated [3H]-inositol (...) phosphate accumulations in [3H]-inositol prelabelled cells. In contrast, the PKC inhibitor, Ro 31-8220, did not affect this response. 3. Histamine (100 microM) or bradykinin (100 nM) evoked rapid increases in inositol 1,4,5-trisphosphate (Ins(1,4,5)P3) and inositol 1,3,4,5-tetrakisphosphate (Ins(1,3,4,5)P4) mass accumulations (maximal accumulations within 10 s and 30 s, respectively) which declined towards basal values over a 10 min incubation period. TPA (1 microM) significantly attenuated the peak Ins

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1992 British journal of pharmacology

3666. Gap junction-mediated cell-to-cell communication in bovine and human adrenal cells. A process whereby cells increase their responsiveness to physiological corticotropin concentrations. (PubMed)

Gap junction-mediated cell-to-cell communication in bovine and human adrenal cells. A process whereby cells increase their responsiveness to physiological corticotropin concentrations. We have studied the role of gap junction-mediated intercellular communication on the steroidogenic response of bovine (BAC) and human (HAC) adrenal fasciculo-reticularis cells in culture to corticotropin (ACTH). Indirect immunofluorescence analyses showed that intact human and bovine adreno-cortical tissue (...) as well as HAC and BAC in culture expressed the gap junction protein connexin43 (also termed alpha 1 connexin). Both HAC and BAC were functionally coupled through gap junctions as demonstrated by microinjection of a low molecular mass fluorescent probe, Lucifer yellow. The cell-to-cell transfer of the probe was blocked by 18 alpha-glycyrrhetinic acid (GA), an inhibitor of gap junction-mediated intercellular communication. GA markedly decreased the steroidogenic response (cortisol production) of both

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1995 Journal of Clinical Investigation

3667. Short-term estradiol treatment enhances pituitary-adrenal axis and sympathetic responses to psychosocial stress in healthy young men. (PubMed)

Short-term estradiol treatment enhances pituitary-adrenal axis and sympathetic responses to psychosocial stress in healthy young men. Evidence from animal studies and clinical observations suggest that the activity of the pituitary-adrenal axis is under significant influence of sex steroids. The present study investigated how a short term elevation of estradiol levels affects ACTH, cortisol, norepinephrine, and heart rate responses to mental stress in healthy men. In a double blind study, 16 (...) men received a patch delivering 0.1 mg estradiol/day transdermally, and age- and body mass index-matched control subjects received a placebo patch. Twenty-four to 48 h later, they were exposed to a brief psychosocial stressor (free speech and mental arithmetic in front of an audience). In response to the psychosocial stressor, ACTH, cortisol, norepinephrine, and heart rate were increased in both experimental groups (all P < 0.0001). However, the estradiol-treated subjects showed exaggerated peak

1996 The Journal of clinical endocrinology and metabolism

3668. Oral dehydroepiandrosterone for adrenal androgen replacement: pharmacokinetics and peripheral conversion to androgens and estrogens in young healthy females after dexamethasone suppression. (PubMed)

mass index 22.5 +/- 1.8 kg/m2) with transient suppression of adrenal androgen secretion because of dexamethasone (dex) administration (4 x 0.5 mg/day for 4 days). Diurnal blood sampling was performed during the early follicular phase of four subsequent menstrual cycles (study period 1: baseline; study periods 2-4: dex + placebo, dex + 50 mg DHEA or dex + 100 mg DHEA in a randomized cross-over design). Dex induced not only a significant suppression of serum cortisol (to 8% of baseline) but also (...) Oral dehydroepiandrosterone for adrenal androgen replacement: pharmacokinetics and peripheral conversion to androgens and estrogens in young healthy females after dexamethasone suppression. Women with adrenal insufficiency suffer from chronic dehydroepiandrosterone (sulfate) [DHEA(S)] deficiency. To define a suitable dose for DHEA replacement, we studied the pharmacokinetics and biotransformation of orally administered DHEA in nine healthy female volunteers (mean age 23.3 +/- 4.1 yr, mean body

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1998 The Journal of clinical endocrinology and metabolism

3669. Growth hormone (GH) responses to GH-releasing hormone alone or combined with arginine in patients with adrenal incidentaloma: evidence for enhanced somatostatinergic tone. (PubMed)

, as a slight degree of cortisol excess may frequently be observed in such patients who do not present with any clear Cushingoid sign. In the present study, 10 patients (3 men and 7 women, aged 48-63 yr) with an adrenal mass discovered serendipitously underwent, on separate occasions, a GHRH injection alone or combined with an infusion of the functional somatostatin antagonist, arginine. Thirteen age-matched healthy volunteers served as controls. Briefly, arginine (30 g) was infused from -30 to 0 min (...) a unilateral uptake of the tracer on the side of the mass with suppression of the contralateral normal adrenal gland. As a group, the patients displayed greater UFC excretion and lower ACTH concentrations than the controls. GH release after GHRH treatment was blunted in patients bearing adrenal incidentaloma compared with controls (GH peak, 5.7 +/- 5.2 vs. 18.0 +/- 7.0 microg/L; P < 0.0001), whereas GHRH plus arginine was able to elicit a comparable response in the 2 groups (GH peak, 33.5 +/- 20.3 vs. 33.7

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2000 The Journal of clinical endocrinology and metabolism

3670. Interactions between the stimulated hypothalamic-pituitary-adrenal axis and leptin in humans. (PubMed)

Interactions between the stimulated hypothalamic-pituitary-adrenal axis and leptin in humans. Leptin, produced by adipocytes, has homeostatic effects on body fat mass through inhibition of appetite and stimulation of the sympathetic nervous system. Several studies have reported that high-dose exogenous glucocorticoids increase circulating leptin concentrations in humans. Conversely, leptin has inhibitory effects on the hypothalamic-pituitary-adrenal (HPA) axis, both at the hypothalamic (...) and adrenal levels. We hypothesized that acute hypercortisolism, in the physiological range, may not alter leptin secretion. Four stimuli of the HPA axis were administered to eight healthy male volunteers in a placebo-controlled study. On separate afternoons, in a randomised order, fasting subjects received i.v. injections of saline, naloxone (125 microg/kg); vasopressin (0.0143 IU/kg); naloxone and vasopressin in combination; or insulin (0.15 U/kg; a dose sufficient to induce hypoglycaemia). Plasma

2000 Journal of neuroendocrinology

3671. Dehydroepiandrosterone replacement in women with adrenal insufficiency: effects on body composition, serum leptin, bone turnover, and exercise capacity. (PubMed)

Dehydroepiandrosterone replacement in women with adrenal insufficiency: effects on body composition, serum leptin, bone turnover, and exercise capacity. Studies in animals and humans using supraphysiological doses of dehydroepiandrosterone (DHEA) reported significant changes in body composition and carbohydrate metabolism. To investigate the metabolic action of a physiological DHEA replacement dose, we studied 24 women with adrenal insufficiency (AI; mean +/- SD age, 42.3 +/- 9.3 yr; duration (...) of disease, 9.2 +/- 8.4 yr; body mass index, 23.4 +/- 4.0 kg/m(2)) in a double blind, placebo-controlled, randomized, cross-over design. They received 50 mg DHEA/day and placebo orally for 4 months each, with a 1 -month washout period. Measurements included fasting serum glucose, insulin, leptin, bone markers, anthropometric parameters determined by bioimpedance analysis, and exercise capacity as assessed by an incremental cycling test. DHEA did not induce any change in body mass index (placebo vs. DHEA

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2001 The Journal of clinical endocrinology and metabolism

3672. Mineralocorticoid receptor blockade by canrenoate increases both spontaneous and stimulated adrenal function in humans. (PubMed)

Mineralocorticoid receptor blockade by canrenoate increases both spontaneous and stimulated adrenal function in humans. Animal studies indicate that mineralocorticoid receptors (MR) in the hippocampus play a major role in the glucocorticoid feedback control of the hypothalamo-pituitary-adrenal (HPA) axis. Specifically, MR mediate the proactive feedback of glucocorticoids in the maintenance of basal HPA activity. The stimulatory effect of intracerebroventricular and intrahippocampal MR blockade (...) on the HPA axis in animals has been clearly shown, whereas the effect of systemic administration of mineralocorticoid antagonists in humans is still contradictory. To clarify this point, in seven normal young women (aged 25-32 yr; body mass index, 19.0-23.0 kg/m(2)) we studied the effects of canrenoate (CAN; 200 mg as iv bolus at 2000 h, followed by 200 mg infused in 500 mL saline over 4 h up to 2400 h) or placebo (saline, 1.0 mL as iv bolus at 2000 h, followed by 500 mL over 4 h up to 2400 h

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2001 The Journal of clinical endocrinology and metabolism

3673. Three Drug Combination Therapy Versus Conventional Treatment of Children With Congenital Adrenal Hyperplasia

the patient's adult height, body mass index, and bone density. ... Condition or disease Intervention/treatment Phase Congenital Adrenal Hyperplasia (CAH) Drug: Flutamide Drug: Letrozole Drug: Hydrocortisone Phase 2 Detailed Description: To test the hypothesis that the regimen of flutamide (an antiandrogen), testolactone or letrozole (an inhibitor of androgen-to-estrogen conversion), and reduced hydrocortisone dose can normalize the growth and adult stature of children with congenital adrenal (...) Three Drug Combination Therapy Versus Conventional Treatment of Children With Congenital Adrenal Hyperplasia Three Drug Combination Therapy Versus Conventional Treatment of Children With Congenital Adrenal Hyperplasia - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies

1999 Clinical Trials

3674. The stimulatory effect of canrenoate, a mineralocorticoid antagonist, on the activity of the hypothalamus-pituitary-adrenal axis is abolished by alprazolam, a benzodiazepine, in humans. (PubMed)

The stimulatory effect of canrenoate, a mineralocorticoid antagonist, on the activity of the hypothalamus-pituitary-adrenal axis is abolished by alprazolam, a benzodiazepine, in humans. Mineralocorticoid receptors (MR) in the hippocampus play a major role in the control of the hypothalamus-pituitary-adrenal (HPA) axis, mediating the proactive feedback of glucocorticoids in the maintenance of basal activity. Intracerebroventricular and intrahippocampal MR blockade stimulates HPA axis in animals (...) of glucocorticoid feedback by metyrapone. We studied the effect of alprazolam (0.02 mg/kg, orally) on the effect of canrenoate (CAN), an MR antagonist (200 mg as an iv bolus, followed by 200 mg infused in 250 ml saline) or placebo on ACTH, cortisol, and dehydroepiandrosterone (DHEA) secretion in six normal young women (aged 25-32 yr; body mass index, 19-23 kg/m(2)). During placebo, ACTH, cortisol, and DHEA secretion showed a progressive decrease (baseline vs. nadir, mean +/- SEM, from 1830-2400 h, 2.6 +/- 0.3

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2002 The Journal of clinical endocrinology and metabolism

3675. Androgen-secreting adrenal adenomas. (PubMed)

Androgen-secreting adrenal adenomas. The androgen source in women with hirsutism and signs of virilism may be the ovary or adrenal gland.Three patients with androgen excess are reported. Two had hyperandrogenemia and Cushing syndrome with an adrenal mass greater than 5.5 cm; the third had a small adrenal adenoma secreting only testosterone and responsive to human chorionic gonadotropin. In all cases, the pathologic report from surgery and the long-term resolution of symptoms confirmed (...) the benign nature of the tumors.Basal and dynamic hormonal tests cannot precisely differentiate ovarian from adrenal tumors. Adrenal adenomas must be considered as a cause of hyperandrogenic syndrome.

2002 Obstetrics and Gynecology

3676. Patients with subclinical Cushing's syndrome due to adrenal adenoma have increased cardiovascular risk. (PubMed)

Patients with subclinical Cushing's syndrome due to adrenal adenoma have increased cardiovascular risk. Subclinical Cushing's syndrome (SCS) is increasingly being reported in incidentally discovered adrenal adenomas; its hallmark is mild autonomous cortisol hyperproduction without specific clinical signs of cortisol excess. Increased prevalence of hypertension, obesity, and impaired glucose tolerance have been described in SCS, but there is no specific study of the risk factors (...) for cardiovascular diseases. In this cross-sectional study we assessed the cardiovascular profile in 28 consecutive SCS patients (19 women and 9 men; aged 56 +/- 10.6 yr) compared with 100 controls matched for age, gender, and body mass index. Systolic (P < 0.001) and diastolic (P < 0.005) blood pressures were higher in patients, as were fasting glucose, insulin, total cholesterol, triglycerides (all P < 0.001), and fibrinogen (P < 0.05). Moreover, the insulin resistance index was increased in patients

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2002 Journal of Clinical Endocrinology and Metabolism

3677. Bone involvement in eugonadal male patients with adrenal incidentaloma and subclinical hypercortisolism. (PubMed)

Bone involvement in eugonadal male patients with adrenal incidentaloma and subclinical hypercortisolism. Adrenal incidentalomas (AI) are not associated, by definition, with clinically evident syndromes; however, some AI patients may show biochemical indexes of subclinical hypercortisolism (SH). Previous data on female AI patients indicated that SH may lead to bone loss, at least at spine. No data are available on bone involvement in samples of only AI male patients. We measured bone metabolism (...) , in order for the most appropriate management to be individually tailored, bone mass evaluation is strongly indicated in AI male patients with SH, irrespective of their gonadal status.

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2002 Journal of Clinical Endocrinology and Metabolism

3678. Adrenal cortical carcinoma. Epidemiology and treatment with mitotane and a review of the literature. (PubMed)

Adrenal cortical carcinoma. Epidemiology and treatment with mitotane and a review of the literature. Adrenal cortical carcinoma is rare; the authors have treated only eight patients with the disease at Good Samaritan Regional Medical Center since 1974. No exhaustive collection of cases of this cancer has been done since 1952.The authors retrospectively reviewed the medical records of their eight patients with adrenal cortical carcinoma. They also searched the English literature from 1952 (...) to 1992 for reports of patients with the disease. They treated each report as a series if two or more previously unreported patients were reported. They paid special attention to patients for whom stage of disease was noted at diagnosis, treatment with mitotane (o,p'-DDD) was used, and the outcome was reported.Five were male and three were female patients. Five had nonfunctional tumors. None were pediatric. The authors found 1891 cases in the English literature. Adrenal cortical carcinomas are more

1993 Cancer

3679. Alteration of the adrenal antioxidant defense system during aging in rats. (PubMed)

to tissue; non enzymatic antioxidants such as vitamin C, E, and glutathione; and tissue antioxidant enzyme (Mn and CuZn superoxide dismutases, catalase, and glutathione peroxidase) activity and expression (mRNA, protein mass, and location). Some measurements were made also on rats maintained on vitamin E-deficient diets. The data show that adrenals from young animals are especially well protected against oxidative events; i.e., these adrenals show the least endogenous lipid peroxidation and the highest (...) Alteration of the adrenal antioxidant defense system during aging in rats. The goal of this study was to determine to what extent aging affects the antioxidant defense system of the rat adrenal and to evaluate the impact of any change in this system on the recognized age-related decline in steroidogenic capacity of adrenocortical cells. The studies were conducted on young (2-5 mo) and aging (12-27 mo) Sprague-Dawley rats and involved procedures measuring steroidogenesis; oxidative damage

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1995 Journal of Clinical Investigation

3680. Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia. (PubMed)

Endocrinology and auxology of sibships with non-classical congenital adrenal hyperplasia. The symptoms, auxological characteristics, and stimulated 17-hydroxyprogesterone (17-OHP) concentrations in a group of patients with non-classical 21-hydroxylase deficiency (NCCAH) were compared with those of their siblings. Ten index cases consisting of nine females and one male patient aged 3-33 years and 16 siblings were studied. In the sibling group five subjects were slightly virilised (...) and body mass index Z scores of the affected patients as a total group or when divided according to skeletal maturity were not significantly different from either the normal mean or from their unaffected siblings. Virilised siblings of patients with NCCAH should have stimulated 17-OHP levels measured to exclude the disease. Patients with NCCAH do not appear to be at risk of short adult stature despite increased bone age in childhood.

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1996 Archives of Disease in Childhood

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