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...
Veröffentlicht in: | Hinyokika kiyo. Acta urologica Japonica. - 1962. - 50(2004), 10 vom: 29. Okt., Seite 691-4 |
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Weitere Verfasser: | , , , |
Format: | Aufsatz |
Sprache: | Japanese |
Veröffentlicht: |
2004
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Zugriff auf das übergeordnete Werk: | Hinyokika kiyo. Acta urologica Japonica |
Schlagworte: | Case Reports Journal Article Review Adrenocorticotropic Hormone 9002-60-2 |
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 |
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Beschreibung: | Date Completed 07.01.2005 Date Revised 01.12.2018 published: Print Citation Status MEDLINE |
ISSN: | 0018-1994 |