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Submitted: 06 June 2007 Modified: 31 July 2017
HERDIN Record #: PCHRD060507120650

Adrenal incidentaloma in a 50 year old male: A case report.

Bernadette R. Asuncion,
Laarnie N. Cale,
Leonisa Sagun,

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Adrenocortical carcinoma (ACC) is a rare neoplasm, usually considered to be one of the most morbid and lethal human tumors due to delayed diagnosis and presence of significant micrometastasis. Incidentalomas detected by diagnostic imaging techniques imposes a great challenge to modern medicine nowadays with regards to proper approach to management. We report a case of a right adrenal mass detected incidentally in an asymptomatic 50 year old Filipino male by ultrasound of abdomen. A CT scan guided fine needle aspiration biopsy was done and adrenal neoplasm was entertained. Vimentin immunoreactivity was noted. Hormonal evaluation was unremarkable. Right adrenalectomy was done and the histopathologic findings revealed features of ACC. Patient expired after a year with recurrence and metastasis despite of chemotherapy and radiotherapy.

Publication Type
Journal
Publication Sub Type
Case report
Title
Philippine Heart Center Journal
Frequency
Annual
Publication Date
January-December 2005
Volume
11
Page(s)
49-52

Objectives

The objective of this paper is to present a case of adrenocortical carcinoma (ACC) in a 50 year old Filipino male as incidentaloma and diagnosed through CT scan-guided FNAB, confirmed by immunostain and histopathologic examination with impact on patient management.

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