Results 11 to 20 of about 6,492 (176)

Cushing's Syndrome [PDF]

open access: yesMedicine, 2005
Abstract Harvey Cushing described the first case of Cushing’s syndrome with a severe phenotype in 1912. Since that time, investigation and management of Cushing’s syndrome has remained a significant clinical challenge and patients suspected of this diagnosis warrant referral to major centres.
openaire   +2 more sources

ACTH-dependent Cushing's Syndrome: Diagnostic Pitfalls in Concomitant Non-secreting Pituitary Adenomas

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2016
Objectives: To describe the possible pitfalls in correctly interpreting clinical, radiological and biochemical findings in ACTH-dependent Cushing's syndrome.
Pietro Lucotti   +4 more
doaj   +1 more source

Subclinical Cushing's Syndrome [PDF]

open access: yesPituitary, 2004
Clinically inapparent adrenal masses, or adrenal incidentalomas, are discovered inadvertently in the course of workup or treatment of unrelated disorders. Cortical adenoma is the most frequent type of adrenal incidentaloma accounting for approximately 50% of cases in surgical series and even greater shares in medical series.
TERZOLO, Massimo   +3 more
openaire   +8 more sources

A challenging case of Cushing’s disease complicated with multiple thrombotic phenomena following trans-sphenoidal surgery; a case report

open access: yesBMC Endocrine Disorders, 2021
Background Cushing’s syndrome occurs due to overproduction of cortisol from adrenal glands. Endogenous hypercortisolemia can occur secondary to adrenocorticotropic hormone (ACTH) dependent as well as independent causes.
Piyumi Sachindra Alwis Wijewickrama   +4 more
doaj   +1 more source

Cushing’s syndrome caused by ACTH precursors secreted from a pancreatic yolk sac tumor in an adult—a case report and literature review

open access: yesFrontiers in Medicine, 2023
Here, we report the first adult case of pancreatic yolk sac tumor with ectopic adrenocorticotropic hormone (ACTH) syndrome. The patient was a 27-year-old woman presenting with abdominal distension, Cushingoid features, and hyperpigmentation.
Johnny Yau Cheung Chang   +12 more
doaj   +1 more source

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

Diagnosis and Treatment of Hypophyseal Cushing’s Syndrome

open access: yesMìžnarodnij Endokrinologìčnij Žurnal, 2014
The paper deals with the questions on etiology, pathogenesis and diagnosis of hypophyseal Cushing’s syndrome. There are described the clinical picture of Cushing’s syndrome as well as the conditions associated with hypercorticoidism in the absence of ...
M.L. Kirilyuk
doaj   +1 more source

Spontaneous bone infarction of the distal femur in a patient with Cushing's disease: a case report

open access: yesBone Reports, 2021
Avascular necrosis of the femoral head is a well-known complication of treatment with high dosage glucocorticoids and has been described in a few patients with Cushing's syndrome.
Pepijn van Houten   +4 more
doaj   +1 more source

Cushing’s Syndrome and Hypothalamic–Pituitary–Adrenal Axis Hyperactivity in Chronic Central Serous Chorioretinopathy

open access: yesFrontiers in Endocrinology, 2018
ObjectiveCentral serous chorioretinopathy (CSC), a specific form of macular degeneration, has been reported as presenting manifestation of Cushing’s syndrome.
Femke M. van Haalen   +8 more
doaj   +1 more source

Cushing's syndrome as a paraneoplastic feature of renal cell carcinoma: A case report

open access: yesUrology Case Reports, 2023
Cushing's syndrome has been believed to be a paraneoplastic syndrome of renal cell carcinomas. However, there appears to be a dearth of compelling evidence to substantiate this notion.
Asaad Moradi   +4 more
doaj   +1 more source

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