Warning: fopen(/home/virtual/enm-kes/journal/upload/ip_log/ip_log_2024-04.txt): failed to open stream: Permission denied in /home/virtual/lib/view_data.php on line 88 Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 89 Radiographic Characteristics of Adrenal Masses in Oncologic Patients
Skip Navigation
Skip to contents

Endocrinol Metab : Endocrinology and Metabolism

clarivate
OPEN ACCESS
SEARCH
Search

Articles

Page Path
HOME > Endocrinol Metab > Volume 31(1); 2016 > Article
Original Article
Clinical Study Radiographic Characteristics of Adrenal Masses in Oncologic Patients
Ji Hyun Lee1, Eun Ky Kim1, A Ram Hong1, Eun Roh1, Jae Hyun Bae1, Jung Hee Kim1, Chan Soo Shin1, Seong Yeon Kim1, Sang Wan Kim1,2orcid
Endocrinology and Metabolism 2016;31(1):147-152.
DOI: https://doi.org/10.3803/EnM.2016.31.1.147
Published online: March 16, 2016

1Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

2Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul National University College of Medicine, Seoul, Korea.

Corresponding author: Sang Wan Kim. Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul National University College of Medicine, 20 Boramae-ro 5-gil, Dongjak-gu, Seoul 07061, Korea. Tel: +82-2-870-2223, Fax: +82-2-870-3863, swkimmd@snu.ac.kr
• Received: August 31, 2015   • Revised: September 30, 2015   • Accepted: October 15, 2015

Copyright © 2016 Korean Endocrine Society

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

  • 4,411 Views
  • 36 Download
  • 9 Web of Science
  • 8 Crossref
  • 13 Scopus
  • Background
    We aimed to assess the usefulness of pre-contrast Hounsfield unit (HU) and mass size on computed tomography to differentiate adrenal mass found incidentally in oncologic patients.
  • Methods
    From 2000 to 2012, 131 oncologic patients with adrenal incidentaloma were reviewed retrospectively. Receiver operating characteristic (ROC) curves were applied to determine the optimal cut-off value of the mean HU and size for detecting adrenal metastasis.
  • Results
    The median age was 18 years, and 80 patients were male. The initial mass size was 18 mm, and 71 (54.2%) of these were on the left side. A bilateral adrenal mass was found in 11 patients (8.4%). Biochemically functional masses were observed in 9.2% of patients. Thirty-six out of 119 patients with nonfunctional masses underwent adrenalectomy, which revealed metastasis in 13. The primary cancers were lung cancer (n=4), renal cell carcinoma (n=2), lymphoma (n=2), hepatocellular carcinoma (n=2), breast cancer (n=1), and others (n=2). The area under the curve for the size and HU for clinically suspicious metastasis were 0.839 (95% confidence interval [CI], 0.761 to 0.900; P<0.001) and 0.959 (95% CI, 0.898 to 0.988; P<0.001), respectively. The cut-off value to distinguish between metastasis and benign masses were 22 mm for size and 20 for HU.
  • Conclusion
    ROC curve results suggest that pre-contrast HU >20 can be used as a diagnostic reference to suggest metastasis in oncologic patients with adrenal masses.
In any patient with a history of cancer, the discovery of adrenal mass requires appropriate diagnostic approaches. Previous studies showed that most of the adrenal incidentalomas (AIs) are benign; however, 2.5% of these cases were metastases to the adrenal gland from another cancers [1]. Most of these results have been suggested in the studies of non-oncologic patients. Furthermore, incidence of incidental metastases was reported to be very low, since these studies excluded patients with known malignancy. Clinical implication of adrenal masses detected in oncologic patients should be distinct from non-oncologic patients. The adrenal gland is a relatively frequent site for metastases in patients with known extra-adrenal cancer. As many as 30% to 40% of lung cancers and 20% to 30% of breast cancers have adrenal metastases [23]. When adrenal masses are detected in cancer patients, it is critical to differentiate between benign adrenal adenoma and metastasis for treatment planning and prediction of prognosis. Patients with adrenal metastases are typically asymptomatic, and the incidence of Addison's disease in a clinical setting is very low. Therefore, imaging diagnosis is crucial for the evaluation of adrenal mass in patients with extra-adrenal cancer. Most cases of AI are often detected on abdominal computed tomography (CT), which is normally performed for reasons other than adrenal diseases. For AI in non-oncologic patients, the tumor size, washout of contrast dye, and noncontrast CT attenuation values expressed in Hounsfield units (HU) are used for distinguishing between benign and malignant adrenal masses [145]. For these patients, common radiographic features of malignant adrenal masses on the CT include a tumor size greater than 4 cm, irregular borders, heterogeneous enhancement, and lesions that demonstrate <40% of the relative percentage washout (RPW) or <60% of the absolute percentage washout (APW) [567].
In previous studies, a cut-off value <10 HU of an adrenal mass increased the likelihood of adenoma sensitivity, and specificity by 71% and 98%, respectively [8]. There are few studies on the radiographic features of AI in patients with extra-adrenal cancer.
In this study, we assessed the usefulness of pre-contrast HU and size of the tumor on CT to differentiate between a benign and malignant adrenal tumor in patients with extra-adrenal cancer.
Institutional Review Board of Seoul National University Hospital approved this retrospective study (#1506-047-679). This study was conducted with AI patients who had been diagnosed previously or concurrently with cancer at the age 18 years or older. Subjects who had clinical symptoms of adrenal disease were excluded.
A total of 156 subjects underwent radiographic and endocrinologic evaluation at our hospital from January 2000 to December 2012. Data were collected from the medical records of patients included the patient's age, sex, presence of distant metastasis, and pathologic reports of adrenal mass after adrenalectomy or fine needle aspiration biopsies. The size, location, and characteristics of all adrenal masses were examined on CT, and the CT findings were based on reports of our radiologists. The pre-contrast HU measurement was obtained in 82.4% of adrenal masses. A circular region of interest was placed over the adrenal mass, and the mean attenuation value was recorded. The longest diameter of the adrenal mass was measured on an image showing the maximal cross-sectional area.
Functional studies were performed included a 24-hour urinary metanephrine, catecholamine, and serum cortisol test, as well as a 24-hour urinary cortisol and overnight 1 mg dexamethasone suppression test (DST). If hypertension was present, the plasma aldosterone concentration and plasma renin activity were measured. Pheochromocytoma was defined as AI with elevated urinary metanephrine and catecholamine levels compared to the reference. A plasma aldosterone/renin ratio of ≥20 was highly suggestive of primary aldosteronism. The saline load test was performed for diagnosis in four out of six patients. The subjects were diagnosed with subclinical Cushing syndrome if the post-overnight DST 8:00 AM serum cortisol level remained above 5 mcg/dL. Subjects with functional tumors, tumors >4 cm, and lesions suspected of being malignant on imaging underwent adrenalectomy, or this technique was performed concurrently with their surgery for primary cancer.
All the masses were categorized as clinically suspicious benign tumors or metastases. To distinguish between benign and malignant tumors, pathologic diagnosis, CT findings, oncologists' opinion, uptake value on [18F]-fluorodeoxyglucose (FDG) positron emission tomography-CT, and reports of magnetic resonance imaging were also included. A lesion was considered malignant if it showed a significant increase or decrease in size over a short period of time. If there was no change in the size for at least 12 months or longer without any cancer treatment, it was defined as clinically suspicious benign tumor. Sixteen subjects were excluded because they had not undergone either a pathological examination or a follow-up CT imaging for at least 12 months. Nine out of 140 subjects with distant metastasis were categorized as indeterminate to differentiate between benign and metastasis. Finally, this study included 131 subjects, and 26 masses were categorized as clinically suspicious metastasis, out of which increased FDG uptake was observed in 20 masses.
Statistical analyses were performed with SPSS version 21.0 (IBM Co., Armonk, NY, USA). The variables were expressed as median and in the interquartile range or as numbers with a percentage. The groups were compared using the Mann-Whitney U test for continuous variables. Receiver operating characteristic (ROC) curve analysis was used to suggest the reference for the size and mean HU for malignant adrenal masses. We compared the area under the curve (AUC) of HU, size, and combination of the HU and size through the pairwise comparison of ROC curves using statistical software, Medcalc (Medcalc, Ostend, Belgium). Statistical significance was indicated as P<0.05 for all tests.
Clinical characteristics of the subjects
A total of 131 oncologic patients with incidentally discovered adrenal masses were included in this study (Fig. 1). The clinical characteristics of the patients are shown in Table 1.
Hormonal evaluation
Twelve or 9.2% of the patients had functioning masses. There were four pheochromocytomas, six cases of primary hyperaldosteronism, and two with subclinical Cushing syndrome. Out of 119 patients (90.8%) with nonfunctioning tumors, 33 underwent adrenalectomy and three had ultrasound-guided biopsy.
Pathologic evaluation
The reason for pathologic diagnosis were tumor size >4 cm (n=6), possible malignancy (n=11), and concurrent operation for primary cancer (n=19, lung lobectomy in one subject, hepatectomy in one, gastrectomy in four, colorectomy in two, and nephrectomy in 11).
Of the above 36 patients, 13 (38.2%) had pathologically proven adrenal metastasis. One patient with diffuse large B-cell lymphoma had bilateral adrenal masses, and histological examination was conducted through ultrasound guided biopsy. A total of six metastases (46.2%) were synchronous with primary cancer.
The primary site of cancers of pathologically proven metastasis were lung cancer (n=3), renal cell carcinoma (n=2), lymphoma (n=2), hepatocellular carcinoma (n=2), breast cancer (n=1), gastric cancer (n=1), rectal cancer (n=1), and neuroblastoma (n=1).
Differentiation between benign and metastatic adrenal masses
Fig. 2 shows a scattergram of the HU and size comparison between clinically suspicious metastasis and benign adenoma. When comparing patients with 13 metastatic lesions and those with 23 benign ones, the median ages of the two groups were comparable (56.0 vs. 60.0, P=0.649). Benign masses ranged in diameter from 8.0 to 45.0 mm (median, 20.0), and the mass size was also significantly different (P=0.02) from those of metastases, which varied from 15.0 to 68.0 mm (median size, 29.0) (Fig. 2A). The HU for benign adrenal masses ranged from –15 to 25 HU (median, 13) and were significantly lower (P<0.001) than those of malignant masses (median, 32 HU; range, 21 to 40) (Fig. 2B). Among 56 subjects who had adrenal mass with HU over 10, 21 (37.5%) performed adrenal CT to differentiate lipid-poor adrenal adenoma from non-adenomatous lesion. There were 15 clinically suspicious benign and six malignant lesions. All 15 clinically suspicious benign lesions demonstrated rapid washout defined as APW of >60% and RPW >40% (Fig. 3). Of the 131 subjects, 119 with nonfunctioning masses were followed up for a period of 3 to 131 months. During the follow-up period, none of the subjects developed functional tumors.
The optimal cut-off value of the tumor size for clinically suspicious metastasis was 22.0 mm (sensitivity 73.1%, specificity 78.5%) and the cut-off value of HU was 20.0 (sensitivity 95.0%, specificity 83.3%) under the ROC curve analysis (Fig. 4). The AUC value for the size and HU were 0.839 (95% confidence interval [CI], 0.761 to 0.900; P<0.001) and 0.955 (95% CI, 0.894 to 0.987; P<0.001), respectively. Increasing the size to 40 mm was associated with higher specificity (98.9%) but lower sensitivity (26.9%). Decreasing the threshold to 10 HU yielded a higher sensitivity (100%) but lower specificity (56.4%).
We confirmed that the AUC for HU (0.959) of the clinically suspicious metastasis was significantly higher than that for the size (0.839) using pairwise comparison of ROC curves (95% CI, 0.005 to 0.196; P=0.038). Moreover, the combination of size and HU showed the largest AUC (AUC, 0.971; 95% CI, 0.932 to 1.000; P<0.001). The AUC was significantly increased in the combination group (0.971) compared with size (0.839) alone (95% CI, 0.022 to 0.204; P=0.015); however, the difference of AUC between combination groups (0.971) and HU (0.939) was not significant (95% CI, –0.0003 to 0.0253; P=0.06).
This results of the retrospective study suggested that the pre-contrast HU and size of the adrenal mass on CT were useful to differentiate benign and metastatic lesions in 131 patients with extra-adrenal cancer. The ROC curve analysis showed the cut-off points for pre-contrast HU and size of the adrenal mass were 20 and 22 mm, respectively.
Previous studies have shown that a threshold value of <10 HU on the pre-contrast CT scans was employed to differentiate benign lesions from indeterminate lesions [91011]. Lipid-rich adenomas demonstrated low attenuation <10 HU due to the presence of intracellular lipids. Non-adenomatous lesions have higher attenuation values since they have a relatively lipid-poor cytoplasm. Non-calcified, non-hemorrhagic adrenal masses with attenuation values >43 HU were proposed to be malignant [12]. Considering these results were from on non-cancer patients, the cut-off value of 20 HU calculated in this study is a relevant threshold value for cancer patients.
In the present study, diameter greater than 22 mm was associated with metastatic adrenal lesions in cancer patients. Lesions larger than 4 cm in diameter are suggested as a surrogate for primary adrenal malignancy [13]; however, the size of metastatic lesions varies and can be bilateral. In fact, only four out of 13 patients with pathologically confirmed tumors showed lesions >4 cm in the present study. Even when metastatic adrenal lesions were clinically defined, the ROC curve analysis showed a cut-off value of 22 mm. These results suggest that the size of adrenal mass >2 cm detected in patients with an extra-adrenal cancer may be suspected for metastasis. However, the use of the size threshold alone has poor specificity regarding the high threshold (size <1.5 cm, specificity 45.2%, sensitivity, 88.5%) and poor sensitivity regarding the specificity (size >4 cm, specificity 98.9%, sensitivity 26.9%). The ROC curve for HU is located to the left of the tumor size, thereby suggesting a larger AUC and a better discriminatory ability. Therefore, HU was considered a better indicator to differentiate between metastasis and adenoma than the mass size, in accordance with previous studies [1114]. Furthermore, combination of HU and size might be more useful than size alone for screening of AI in oncologic patients. In this study, the lung was the most common primary malignant site, followed by the kidney, liver, and lymph node. These results are in close agreement with those of previous reports, including a study of 464 patients with adrenal metastases over a 30-year period [1516]. These indicate that the patient population in this study was not so distinct from other studies. However, this study has limitations, such as lack of contrast washout data in some cases and retrospective design of patients in a single center.
In conclusion, according to us, a pre-contrast value >20 HU on CT may be more useful than the mass size to differentiate metastasis from benign lesions detected incidentally in patients with extra-adrenal cancer.

CONFLICTS OF INTEREST: No potential conflict of interest relevant to this article was reported.

  • 1. Mansmann G, Lau J, Balk E, Rothberg M, Miyachi Y, Bornstein SR. The clinically inapparent adrenal mass: update in diagnosis and management. Endocr Rev 2004;25:309–340. ArticlePubMedPDF
  • 2. Gittens PR Jr, Solish AF, Trabulsi EJ. Surgical management of metastatic disease to the adrenal gland. Semin Oncol 2008;35:172–176. ArticlePubMed
  • 3. Lumb G, Mackenzie DH. The incidence of metastases in adrenal glands and ovaries removed for carcinoma of the breast. Cancer 1959;12:521–526. ArticlePubMed
  • 4. Young WF Jr. Clinical practice. The incidentally discovered adrenal mass. N Engl J Med 2007;356:601–610. ArticlePubMed
  • 5. Kapoor A, Morris T, Rebello R. Guidelines for the management of the incidentally discovered adrenal mass. Can Urol Assoc J 2011;5:241–247. ArticlePubMedPMC
  • 6. Caoili EM, Korobkin M, Francis IR, Cohan RH, Platt JF, Dunnick NR, et al. Adrenal masses: characterization with combined unenhanced and delayed enhanced CT. Radiology 2002;222:629–633. ArticlePubMed
  • 7. Johnson PT, Horton KM, Fishman EK. Adrenal mass imaging with multidetector CT: pathologic conditions, pearls, and pitfalls. Radiographics 2009;29:1333–1351. ArticlePubMed
  • 8. Anagnostis P, Karagiannis A, Tziomalos K, Kakafika AI, Athyros VG, Mikhailidis DP. Adrenal incidentaloma: a diagnostic challenge. Hormones (Athens) 2009;8:163–184. ArticlePubMed
  • 9. Sahdev A, Reznek RH. The indeterminate adrenal mass in patients with cancer. Cancer Imaging 2007;7(Spec No A):S100–S109. ArticlePubMedPMC
  • 10. Boland GW, Lee MJ, Gazelle GS, Halpern EF, McNicholas MM, Mueller PR. Characterization of adrenal masses using unenhanced CT: an analysis of the CT literature. AJR Am J Roentgenol 1998;171:201–204. ArticlePubMed
  • 11. Hamrahian AH, Ioachimescu AG, Remer EM, Motta-Ramirez G, Bogabathina H, Levin HS, et al. Clinical utility of noncontrast computed tomography attenuation value (hounsfield units) to differentiate adrenal adenomas/hyperplasias from nonadenomas: Cleveland Clinic experience. J Clin Endocrinol Metab 2005;90:871–877. ArticlePubMedPDF
  • 12. Blake MA, Kalra MK, Sweeney AT, Lucey BC, Maher MM, Sahani DV, et al. Distinguishing benign from malignant adrenal masses: multi-detector row CT protocol with 10-minute delay. Radiology 2006;238:578–585. ArticlePubMed
  • 13. Grumbach MM, Biller BM, Braunstein GD, Campbell KK, Carney JA, Godley PA, et al. Management of the clinically inapparent adrenal mass ("incidentaloma"). Ann Intern Med 2003;138:424–429. ArticlePubMed
  • 14. Gopan T, Remer E, Hamrahian AH. Evaluating and managing adrenal incidentalomas. Cleve Clin J Med 2006;73:561–568. ArticlePubMed
  • 15. Lam KY, Lo CY. Metastatic tumours of the adrenal glands: a 30-year experience in a teaching hospital. Clin Endocrinol (Oxf) 2002;56:95–101. ArticlePubMed
  • 16. Xu B, Gao J, Cui L, Wang H, Guan Z, Yao S, et al. Characterization of adrenal metastatic cancer using FDG PET/CT. Neoplasma 2012;59:92–99. ArticlePubMed
Fig. 1

Flow chart of follow-up for cancer patients with adrenal incidentaloma (AI). PET-CT, positron emission tomography-computed tomography; MRI, magnetic resonance imaging; FNA, fine needle aspiration.

enm-31-147-g001.jpg
Fig. 2

(A) Adrenal size and (B) Hounsfield unit (HU) for clinically suspicious benign (b) and metastasis (m).

enm-31-147-g002.jpg
Fig. 3

(A) Absolute percentage washout (APW) and (B) relative percentage washout (RPW) in case adrenal mass with Hounsfield unit over 10. b, clinically suspicious benign; m, clinically suspicious metastasis.

enm-31-147-g003.jpg
Fig. 4

Receiver operating characteristic curve for adrenal mass defined as clinically suspicious metastasis. HU, Hounsfield unit; PPV, positive predictive value; NPV, negative predictive value; AUC, area under the curve; CI, confidence interval.

enm-31-147-g004.jpg
Table 1

Clinical Characteristics of Cancer Patients with AI (n=131)

enm-31-147-i001.jpg
Characteristic Value
Sex, male:female 80:51
Age, yr 57 (51–66)
Tumor size, widest diameter in mm 18 (13–25)
Follow-up duration, yr 2.8 (1.6–5.0)
Non-contrast, Hounsfield unit 15 (3–24)
Location of the tumor
 Left 71 (54.2)
 Right 49 (37.4)
 Both 11 (8.4)
Distant metastasis 29 (21.8)
Clinically suspicious metastasis 26/131 (19.8)
Pathologically proven metastasis 13/47 (27.7)

Values are presented as median (interquartile range) or number (%).

Figure & Data

References

    Citations

    Citations to this article as recorded by  
    • Risk of malignancy in adrenal tumors in patients with a history of cancer
      Radosław Samsel, Karolina Nowak, Lucyna Papierska, Edyta Karpeta, Katarzyna Roszkowska-Purska, Wacław Smiertka, Tomasz Ostrowski, Eryk Chrapowicki, Alan Grabowski, Dorota Leszczyńska, Andrzej Cichocki
      Frontiers in Oncology.2023;[Epub]     CrossRef
    • Adrenal Tumors Found During Staging and Surveillance for Colorectal Cancer: Benign Incidentalomas or Metastatic Disease?
      Mio Yanagisawa, Dania G. Malik, Thomas W. Loehfelm, Ghaneh Fananapazir, Michael T. Corwin, Michael J. Campbell
      World Journal of Surgery.2020; 44(7): 2282.     CrossRef
    • Predictive factors for adrenal metastasis in extra‐adrenal malignancy patients with solitary adrenal mass
      Kyeong‐Hyeon Byeon, Yun‐Sok Ha, Seock‐Hwan Choi, Bum Soo Kim, Hyun Tae Kim, Eun Sang Yoo, Tae Gyun Kwon, Jun Nyung Lee, Tae‐Hwan Kim
      Journal of Surgical Oncology.2018; 118(8): 1271.     CrossRef
    • Combining Washout and Noncontrast Data From Adrenal Protocol CT
      Chaan S. Ng, Emre Altinmakas, Wei Wei, Payel Ghosh, Xiao Li, Elizabeth G. Grubbs, Nancy A. Perrier, Victor G. Prieto, Jeffrey E. Lee, Brian P. Hobbs
      Academic Radiology.2018; 25(7): 861.     CrossRef
    • Evaluation of quantitative parameters for distinguishing pheochromocytoma from other adrenal tumors
      Youichi Ohno, Masakatsu Sone, Daisuke Taura, Toshinari Yamasaki, Katsutoshi Kojima, Kyoko Honda-Kohmo, Yorihide Fukuda, Koji Matsuo, Toshihito Fujii, Akihiro Yasoda, Osamu Ogawa, Nobuya Inagaki
      Hypertension Research.2018; 41(3): 165.     CrossRef
    • Articles inEndocrinology and Metabolismin 2016
      Won-Young Lee
      Endocrinology and Metabolism.2017; 32(1): 62.     CrossRef
    • The Diverse Clinical Presentations of Adrenal Lymphoma
      Awais Masood, Anna Tumyan, Daniel R. Nussenzveig, Dara N. Wakefield, Diana Barb, Hans K. Ghayee, Naim M. Maalouf
      AACE Clinical Case Reports.2017; 3(4): 307.     CrossRef
    • Optimal follow-up strategies for adrenal incidentalomas: reappraisal of the 2016 ESE-ENSAT guidelines in real clinical practice
      A Ram Hong, Jung Hee Kim, Kyeong Seon Park, Kyong Young Kim, Ji Hyun Lee, Sung Hye Kong, Seo Young Lee, Chan Soo Shin, Sang Wan Kim, Seong Yeon Kim
      European Journal of Endocrinology.2017; 177(6): 475.     CrossRef

    • PubReader PubReader
    • Cite
      CITE
      export Copy
      Close
    • XML DownloadXML Download
    Figure

    Endocrinol Metab : Endocrinology and Metabolism