Adrenocorticotropic hormone-secreting adrenal pheochromocytoma : a case report

A 55-year-old woman with transient faintness was referred to our hospital. Laboratory studies showed high levels of plasma catecholamines, cortisol, adrenocorticotropic hormone (ACTH) and urinary vanyl mandelic acid (VMA). Abdominal computed tomography (CT) showed a right adrenal tumor measuring 4.5...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Hinyokika kiyo. Acta urologica Japonica. - 1962. - 50(2004), 10 vom: 29. Okt., Seite 691-4
1. Verfasser: Tanikawa, Go (VerfasserIn)
Weitere Verfasser: Ueda, Tomohiro, Nakamura, Yoshihiro, Hosomi, Masahiro, Kirohara, Hisakazu
Format: Aufsatz
Sprache:Japanese
Veröffentlicht: 2004
Zugriff auf das übergeordnete Werk:Hinyokika kiyo. Acta urologica Japonica
Schlagworte:Case Reports Journal Article Review Adrenocorticotropic Hormone 9002-60-2
Beschreibung
Zusammenfassung:A 55-year-old woman with transient faintness was referred to our hospital. Laboratory studies showed high levels of plasma catecholamines, cortisol, adrenocorticotropic hormone (ACTH) and urinary vanyl mandelic acid (VMA). Abdominal computed tomography (CT) showed a right adrenal tumor measuring 4.5 cm diameter that was enhanced heterogeneously by contrast medium. Brain CT and chest CT did not detect any other tumors. Under the clinical diagnosis of ectopic ACTH secreting adrenal pheochromocytoma, we performed right adrenalectomy. Pathological findings showed pheochromocytoma, and tumor cells were heterogeneously stained by anti-ACTH antibody
Beschreibung:Date Completed 07.01.2005
Date Revised 01.12.2018
published: Print
Citation Status MEDLINE
ISSN:0018-1994