Diagnostic and therapeutic management of patients with adrenal incidentaloma

Routine and frequent use of computerized tomography (CT) angiography in vascular disease detection has led to frequent suprarenal gland abnormal findings that could, if undiagnosed, significantly complicate the course of the future treatment. The term adrenal incidentaloma refers to adrenal lesion discovered serendipitously during an imaging investigation. Adrenal incidentalomas do not constitute a single pathological entity. Major concerns are risks of malignancy and autonomous hormone secretion. The majority of all adrenal incidentalomas (approximately 79%) are nonfunctioning benign lesions. Among functioning lesions subclinical cortisol excess is most frequently found. All patients with adrenal incidentaloma should undergo clinical, biochemical, and imaging evaluation for malignancy and hormone production. In this review, we discuss the current issues in diagnostic and therapeutic management of patients with adrenal incidentaloma. Follow-up of patients with adrenal incidentalomas involves the assessment of growth and development of hormonal function. After this review analysis several useful protocols could be designed to help vascular surgeons to adequately treat patients with concomitant vascular disease and adrenal incidentaloma.

[1]  P. Chaffanjon,et al.  Is Adrenal Venous Sampling Mandatory before Surgical Decision in Case of Primary Hyperaldosteronism? , 2014, World Journal of Surgery.

[2]  S. Vujović,et al.  Nondiabetic patients with either subclinical Cushing's or nonfunctional adrenal incidentalomas have lower insulin sensitivity than healthy controls: clinical implications. , 2013, Metabolism: clinical and experimental.

[3]  L. Brunt,et al.  Evaluation and management of adrenal incidentaloma , 2012, Journal of surgical oncology.

[4]  S. Nakanishi,et al.  Influence of Adrenal Subclinical Hypercortisolism on Hypertension in Patients with Adrenal Incidentaloma , 2012, Experimental and Clinical Endocrinology & Diabetes (Barth).

[5]  D. Aron,et al.  Adrenal incidentalomas. , 2012, Best practice & research. Clinical endocrinology & metabolism.

[6]  G. Arnaldi,et al.  Adrenal incidentaloma. , 2012, Best practice & research. Clinical endocrinology & metabolism.

[7]  S. Tsagarakis,et al.  Endocrine incidentalomas—challenges imposed by incidentally discovered lesions , 2011, Nature Reviews Endocrinology.

[8]  A. Grossman,et al.  The clinical significance of adrenal incidentalomas , 2011, European journal of clinical investigation.

[9]  A. Pontecorvi,et al.  The size of adrenal incidentalomas correlates with insulin resistance. Is there a cause‐effect relationship? , 2011, Clinical endocrinology.

[10]  L. Nieman,et al.  Approach to the patient with an adrenal incidentaloma. , 2010, The Journal of clinical endocrinology and metabolism.

[11]  Elliot K Fishman,et al.  Adrenal mass imaging with multidetector CT: pathologic conditions, pearls, and pitfalls. , 2009, Radiographics : a review publication of the Radiological Society of North America, Inc.

[12]  H. Unalp,et al.  Cardiovascular Risk in Patients with Nonfunctional Adrenal Incidentaloma: Myth or Reality? , 2009, World Journal of Surgery.

[13]  A. Comlekçi,et al.  Carotid intima media thickness is increased and associated with morning cortisol in subjects with non-functioning adrenal incidentaloma , 2009, Endocrine.

[14]  A. Tischler,et al.  Pheochromocytoma: recommendations for clinical practice from the First International Symposium , 2007, Nature Clinical Practice Endocrinology &Metabolism.

[15]  Martin Fassnacht,et al.  Adrenocortical Carcinoma: Clinical Update , 2006 .

[16]  M. Fassnacht,et al.  Adrenocortical carcinoma -- improving patient care by establishing new structures. , 2006, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

[17]  G. Reimondo,et al.  Subclinical Cushing's syndrome in adrenal incidentalomas. , 2005, Endocrinology and metabolism clinics of North America.

[18]  I. Gill,et al.  Comparison of CT findings in symptomatic and incidentally discovered pheochromocytomas. , 2005, AJR. American journal of roentgenology.

[19]  B. Ambrosi,et al.  Midnight serum cortisol as a marker of increased cardiovascular risk in patients with a clinically inapparent adrenal adenoma. , 2005, European journal of endocrinology.

[20]  E. Balk,et al.  The clinically inapparent adrenal mass: update in diagnosis and management. , 2004, Endocrine reviews.

[21]  M. Stowasser,et al.  Primary aldosteronism—careful investigation is essential and rewarding , 2004, Molecular and Cellular Endocrinology.

[22]  G. Braunstein,et al.  Management of the Clinically Inapparent Adrenal Mass (Incidentaloma) , 2003, Annals of Internal Medicine.

[23]  H. Sasano,et al.  Analysis of cortisol secretion in hormonally inactive adrenocortical incidentalomas: study of in vitro steroid secretion and immunohistochemical localization of steroidogenic enzymes. , 2001, Endocrine journal.

[24]  J. Moley,et al.  Adrenal locidentaloma , 2001, World Journal of Surgery.

[25]  D. Mitchell,et al.  Distinction between benign and malignant adrenal masses: value of T1-weighted chemical-shift MR imaging. , 1995, AJR. American journal of roentgenology.

[26]  G. Griffing A-I-D-S: the new endocrine epidemic. , 1994, The Journal of clinical endocrinology and metabolism.