Cited by 56Adrenal and Paraganglionic TumorsPituitary Gland Disorders and TreatmentsNeuroendocrine Tumor Research Advances

Incidentally Discovered Adrenal Tumors: A Lesson from Observation of 1444 Patients

Kasperlik-Załuska, A., Otto, M., Cichocki, A., Rosłonowska, E., Słowińska-Srzednicka, J., Jeske, W., Papierska, L., Zgliczyński, W.·2008·Hormone and Metabolic Research

Abstract

This study was aimed at summarizing our experience in the management of 1,444 patients with incidentally found adrenal tumors observed at a single endocrinological centre. Hormonal determinations were performed in all patients at the beginning of the observation period to detect subclinical adrenal hyperfunction. The imaging phenotype on CT and MRI was analyzed for defining the malignant potential of the tumors. Based on the results of these examinations we diagnosed among our cohort probably benign masses in 87%, malignant tumors in 10% (adrenal carcinoma - 9%), and metastases in 3%. Subclinical hyperfunction was diagnosed in 8%; the most frequent was the pre-Cushing's syndrome. A subgroup of 480 patients (33%) was submitted to surgery because of oncological or endocrinological indications. The patients not qualified for surgery were carefully controlled by imaging and hormonal examinations. Malignancy is the most serious risk in the group of patients with incidentally discovered adrenal tumors.

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Crossref · 10.1055/s-2008-1073167

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  • Previous imaging studies have reported that AIs are more common in females; however, this has not been observed in autopsy studies.

    “Previous imaging studies have reported that AIs are more common in females (66,71,73); however, this has not been observed in autopsy studies (11,85).”

    From Adrenal incidentaloma (2020) · cites this paper as [71]

  • All studies consistently report a higher incidence of ACC if the adrenal mass is greater than 4 cm in size.

    “However, it should be noted that all studies consistently report a higher incidence of ACC if the adrenal mass is greater than 4 cm in size (39,49,63,66,71).”

    From Adrenal incidentaloma (2020) · cites this paper as [71]

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Authors
Kasperlik-Załuska, A., Otto, M., Cichocki, A., Rosłonowska, E., Słowińska-Srzednicka, J., Jeske, W., Papierska, L., & Zgliczyński, W.
Venue
Hormone and Metabolic Research
Published
2008-05
Volume
40
Issue
5
Pages
338-341
ISSN
  • 0018-5043 (ISSN-L)
  • 1439-4286
OpenAlex
W1989982630
Cited by
56
References
0
Citations by year
2026: 1 · 2025: 2 · 2024: 2 · 2023: 2 · 2022: 5 · 2021: 1 · 2020: 2 · 2018: 3 · 2017: 3 · 2016: 1 · 2015: 7 · 2014: 2 · 2013: 5 · 2012: 5
FWCI
5.27
Type
journal article
Language
en
Open access
closed
Locations
  • Hormone and Metabolic Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
  • Health Sciences › Medicine › Epidemiology › Neuroendocrine Tumor Research Advances
Keywords
incidental adrenal tumor, adrenal incidentaloma, adrenocortical carcinoma, adrenal metastasis, CT and MRI imaging features, surgical management, long-term follow-up
MeSH terms
Adolescent, Adrenal Gland Neoplasms, Adult, Aged, Aged, 80 and over, Child, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neoplasms, Retrospective Studies, Tomography, X-Ray Computed

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