Case Reports

Adult Adrenocortical Carcinoma Mass with Extension into the Inferior Vena Cava and Cushingoid Features: a Rare Case with the Review of Literature

Abstract

Adrenocortical carcinomas (ACC) is an uncommon disease that accounts for only 0.02% of all cancers. Herein, this study evaluates a case of adult ACC with extension into the inferior vena cava and Cushingoid features. A 67-year-old lady was admitted to the surgery service for surgical resection of adrenal mass which was found on hypertension work-up. On physical examination, she was fat, cushingoid and had ecchymoses on her skin. The patient was hypokalemic at the time of admission. Spiral CT with contrast of the abdomen and pelvis was done and showed solid mass measuring 10x11 cm, upper to the right kidney and posterior to IVC (inferior vena cava) with anterior displacement of IVC. Microscopic diagnosis was adrenocortical carcinoma with vascular invasion and necrosis (20% of surface area) in this case. In conclusion, the hypertension can be the most common complaints in ACC patients and probably, the existence of both hypertension and hypokalemia in a case can increase suspicion of ACC that it needs to future studies with focus on these complaints.

Weissferdt A, Phan A, Suster S, Moran CA. Adrenocortical carcinoma: a comprehensive immunohistochemical study of 40 cases. Appl Immunohistochem Mol Morphol. 2014;22:24-30.

Ruotolo G, Ambrosio MR, Caroleo PR, Bonacci E, Condito AM, Merante A, et al. Adrenal incidentaloma: a case of carcinoma. Clin Interv Aging. 2010;5:31-5.

Peppa M, Pikounis V, Papaxoinis G, Macheras A, Economopoulos T, Raptis SA, et al. Adrenocortical carcinoma secreting cortisol, androgens and aldosterone: a case report. Cases J. 2009;2:8951.

Paiboon C. Adrenocortical Carcinoma: A Case Report. Thai Cancer J.2015;36:1-6.

Allolio B, Fassnacht M. Clinical review: Adrenocortical carcinoma: clinical update. J Clin Endocrinol Metab. 2006;91:2027–2037.

Else T, Kim AC, Sabolch A, Raymond VM, Kandathil A, Caoili EM, et al. Adrenalcortical carcinoma. Endocrine Rev. 2014;35:282–326.

Fulawka L, Patrzalek D, Halon A. Adrenal cortical carcinoma with extension into the inferior vena cava--case report and literature review. Diagn Pathol. 2014;9:51.

Aghamohammadzadeh N, Faraji A, Bozorgi F, Faraji I, Moghadaszadeh M. Primary hyperaldostronisim as initial presentation of adrenal cortical carcinoma with liver metastasis: a case report. Int J Hematol Oncol Stem Cell Res. 2013;7:38-42.

Pommier RF, Brennan MF. An eleven-year experience with adrenocortical carcinoma. Surgery. 1992;112:963–71.

Aparna C, Renuka IV, Saila Bala G, Annapurna P. Adrenocortical carcinoma: Report of two cases. Indian J Endocrinol Metab. 2011;15:217-9.

Nakanoma T, Ueno M, Nonaka S, Tsukamoto T, Deguchi N. [Left adrenocortical cancer with inferior vena cava tumor thrombus--a case report]. Nihon Hinyokika Gakkai Zasshi. 2001;92:34-7.

Wang Y, Zhou F, Pan H, Jin B. Adrenal cortical carcinoma with tumor thrombus extension into the right atrium: A case report. Oncol Lett. 2016;11:3987-3991.

Kashiwagi S, Amano R, Onoda N, Noda S, Hirata K, Asano Y, et al. Nonfunctional adrenocortical carcinoma initially presenting as retroperitoneal hemorrhage. BMC Surg. 2015;15:46.

Almarzouq A, Asfar S, Hussain S, Al-Hunayan A, Aldousari S. Giant nonfunctioning adrenocortical carcinoma: a case report and review of the literature. BMC Res Notes. 2014;7:769.

Naffaa ME, Ilivitzki A, Braun E. Adrenocortical carcinoma presenting as bilateral pitting leg oedema. BMJ Case Rep. 2014;2014.

Ni H, Htet A. Adrenal cortical carcinoma masquerading as pheochromocytoma: a case report. Ecancermedicalscience. 2012;6:277.

Carlson AL, Marney AM, Anderson SR, Gilbert MP. Bilateral adrenal incidentalomas: a case report and review of diagnostic challenges. Case Rep Endocrinol. 2013;2013:953052.

Lele SM, Mittal BV, Vora IM, Kulkarni HS. Nonfunctioning adrenocortical carcinoma. J Postgrad Med. 1992;38:145-7.

Chung JO, Cho DH, Lee JH, Kwon DD, Chung DJ, Chung MY. Spontaneous rupture of a functioning adrenocortical carcinoma. Yonsei Med J. 2010;51:974-7.

Stamoulis JS, Antonopoulou Z, Safioleas M. Haemorrhagic shock from the spontaneous rupture of an adrenal cortical carcinoma. A case report. Acta Chir Belg. 2004;104:226-8.

Vilchis-Cárdenas Marco A, López-Verdugo José F, Aragón-Tovar Anel R, Torres-Medina Eduardo, Saldaña-Guajardo Mario J, García-Rodríguez Miguel A, et al. Adrenocortical carcinoma: a case report and literature review. Rev Mex Urol. 2011;71:47-56.

Choi JH, So YR, Hwang YC, Jeong IK, Ahn KJ, Chung HY, et al. [A Case of Adrenocortical Carcinoma Secreting Cortisol, Androgen and Aldosterone]. Endocrinol Metab. 2011;26:239-242.

Mezhir JJ, Song J, Piano G, Testa G, Raman J, Al-Ahmadie HA, et al. Adrenocortical carcinoma invading the inferior vena cava: case report and literature review. Endocr Pract. 2008;14:721-5.

Annamaria P, Silvia P, Bernardo C, Alessandro de L, Antonino M, Antonio B, et al. Adrenocortical carcinoma with inferior vena cava, left renal vein and right atrium tumor thrombus extension. Int J Surg Case Rep. 2015;15:137-9.

Files
IssueVol 9 No 1 (2017) QRcode
SectionCase Reports
Keywords
Adrenocortical carcinoma Cushingoid Inferior vena cava

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Ramezani M, Kavousi F, Amirian F, Sadeghi M. Adult Adrenocortical Carcinoma Mass with Extension into the Inferior Vena Cava and Cushingoid Features: a Rare Case with the Review of Literature. Basic Clin Cancer Res. 2017;9(1):40-45.