Results 81 to 90 of about 5,534 (205)

Functioning ganglioneuroma of the adrenal gland - case report and review of literature

open access: yesIndian Journal of Urology, 2001
A ganglioneuroma of adrenal gland in a 34-year-old female presenting as adrenal incidentaloma is described. The significance of this finding is discussed, and litera-ture in English is reviewed to highlight the importance of hormonal evaluation of an ...
Anand Kumar Mishra   +7 more
doaj  

Adrenal Myelolipoma- A Rare Case Report [PDF]

open access: yesAl Ameen Journal of Medical Sciences, 2009
Adrenal myelolipoma (AML) is a rare benign tumour composed of mature adipose tissue and hematopoietic tissue. Very few cases have been reported. Most of these patients are asymptomatic.
Vijayalaxmi V. Suranagi   +4 more
doaj  

A rare presentation of right adrenal angiomyolipoma with accelerated hypertension: A case report

open access: yesArchives of Clinical and Experimental Surgery, 2018
Right adrenal angiomyolipoma with accelerated hypertension is usually an incidentaloma and infrequent finding, and only adrenal angiomyolipomas are reported but not with tumor-associated accelerated hypertension.
Hari Hasan Chunchu   +4 more
doaj   +1 more source

Rare Association Between Neurofibromatosis Type 1 and Adrenocortical Carcinoma

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
Axial slice CT abdomen pelvis with portal venous contrast, revealing a well circumscribed 22 × 20 × 22 mm left adrenocortical adenocarcinoma (ACC) in a patient with neurofibromatosis type 1 (NF1). ABSTRACT Although rare, adrenocortical carcinoma (ACC) should be considered in individuals with neurofibromatosis type 1 (NF1) presenting with adrenal ...
Zachary Pluim   +6 more
wiley   +1 more source

A Hidden Culprit: Aldosteronoma as a Rare Cause of Refractory Hypertension in Autosomal‐Dominant Polycystic Kidney Disease

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Hypertension is common in autosomal‐dominant polycystic kidney disease (ADPKD) but may occasionally reflect a secondary etiology. We report a 71‐year‐old man with ADPKD and end‐stage renal disease who developed persistent, refractory hypertension following renal transplantation despite multidrug therapy and bilateral native nephrectomy ...
Matthew Wainstein   +7 more
wiley   +1 more source

Adrenal incidentalomas

open access: yesBritish Journal of Surgery, 2022
Eleni, Hadjikyriacou, Richard, Egan
openaire   +2 more sources

A Pheochromocytoma Case Diagnosed As Adrenal Incidentaloma [PDF]

open access: yes, 2017
There are two problems that needs to be addressed in cases of an adrenal incidentaloma. The first is to decide whether the adrenal mass is benign or malignant, and the second is to determine whether the mass is hormonally active or not.
Orhan, Diclehan   +15 more
core   +1 more source

Optic Nerve Incidentaloma

open access: yes, 2017
Retinal astrocytic hamartomas are rare, benign tumors of glial origin. These lesions are often associated with systemic syndromes, including tuberous sclerosis complex and neurofibromatosis type 1, but also may be encountered in otherwise healthy ...
Eric J. Sigler   +2 more
core   +1 more source

Incidentaloma adrenal : estudio descriptivo de una serie

open access: yes, 2021
El incidentaloma adrenal es aquella masa suprarrenal hallada casualmente al realizar una prueba de imagen por otro motivo. El estudio debe determinar su benignidad y funcionalidad. La controversia radica en el seguimiento.
Universitat Autònoma de Barcelona. Facultat de Medicina   +2 more
core  

WFUMB position paper on the management incidental findings:Adrenal incidentaloma

open access: yes, 2020
Focal lesions of the adrenal glands are incidentally detected in approximately 5% of cases by modern imaging techniques. Fewer than 5% of these adrenal incidentalomas are malignant and approximately 10% have endocrine activity.
Dong, Yi   +5 more
core   +1 more source

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