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Co-Existing Ectopic Cortisol-Producing Adenoma and Retroperitoneal Schwannoma, a Rare Case Report.
Diabetes Metab Syndr Obes
November 2024
Third Military Medical University (Army Medical University), Chongqing, People's Republic of China.
Background: Ectopic cortisol-producing adrenocortical adenoma (ECPA) is extremely rare, with only a few cases reported. Retroperitoneal schwannoma is also uncommon, accounting for only 0.7-5% of all schwannomas.
View Article and Find Full Text PDFExtra-adrenal adrenocortical cancer associated with multiple endocrine neoplasia type 1.
Endocrinol Diabetes Metab Case Rep
October 2024
Department of Endocrinology, Beaumont Hospital, Dublin, Ireland.
Summary: Adrenocortical carcinoma (ACC) is a rare malignant tumour arising from the adrenal cortex, with an estimated annual incidence of one to two patients per million. Ectopic ACCs are extremely rare. The majority of ACCs are sporadic; however, ACC has been linked with genetic disease processes, including multiple endocrine neoplasia type-1 (MEN-1).
View Article and Find Full Text PDFEctopic adrenocortical adenoma in the abdominal wall linked to the head of the pancreas: A case report.
Int J Surg Case Rep
December 2024
Faculty of Medicine, Tishreen University, Latakia, Syria.
Article Synopsis
Challenging Diagnostic Workup of a 22-year-old Patient With Primary Pigmented Nodular Adrenocortical Disease.
JCEM Case Rep
October 2024
Diagnostic and Research Institute of Pathology, Medical University of Graz, 8010 Graz, Austria.
Article Synopsis
- Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of ACTH-independent Cushing syndrome (CS) that complicates diagnosis due to its similarities with other conditions.* -
- A 22-year-old female exhibited classic symptoms like weight gain and moon facies, but imaging tests showed normal adrenal glands, making it difficult to find the source of cortisol overproduction.* -
- Ultimately, adrenal vein sampling confirmed cortisol came from the adrenal glands, leading to successful treatment through bilateral adrenalectomy and a diagnosis of PPNAD linked to a genetic mutation associated with the Carney complex.*
A puzzling malignant adrenal tumor.
Ann Endocrinol (Paris)
December 2024
Department of Endocrinology, Santo António Local Health Unit, Largo Professor Abel Salazar, 4099-001 Porto, Portugal.
A previously healthy 49-year-old male presented with abdominal pain, constitutional syndrome, paroxysmal palpitations and diaphoresis. Full-body CT scan showed a large malignant adrenal mass with abdominal lymph node and pulmonary metastasis. Biochemical studies revealed hypersecretion of catecholamines, cortisol, sexual steroids and steroid precursors; ACTH was not suppressed, and chromogranin A was negative.
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