A case of adrenocortical adenoma harboring venous thrombus mimicking adrenal malignancy
Author:
Affiliation:
1. Department of Endocrinology, Diabetes and Metabolism, Kitasato University School of Medicine, Sagamihara, Kanagawa 252-0374, Japan
2. Department of Pathology, Tohoku University School of Medicine, Sendai, Miyagi 980-8575, Japan
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.jstage.jst.go.jp/article/endocrj/68/7/68_EJ20-0667/_pdf
Reference27 articles.
1. 1 Kim J, Bae KH, Choi YK, Jeong H, Je D, et al. (2013) Clinical characteristics for 348 patients with adrenal incidentaloma. Endocrinol Metab (Seoul) 28: 20–25.
2. 2 Pasternak JD, Seib CD, Seiser N, Tyrell JB, Liu C, et al. (2015) Differences between bilateral adrenal incidentalomas and unilateral lesions. JAMA Surg 150: 974–978.
3. 3 Koch CA, Pacak K, Chrousos GP (2002) The molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors. J Clin Endocrinol Metab 87: 5367–5384.
4. 4 Majnik J, Patocs A, Balogh K, Toth M, Gergics P, et al. (2006) Overrepresentation of the N363S variant of the glucocorticoid receptor gene in patients with bilateral adrenal incidentalomas. J Clin Endocrinol Metab 91: 2796–2799.
5. 5 Patocs A, Toth M, Barta C, Sasvari-Szekely M, Varge I, et al. (2002) Hormonal evaluation and mutation screening for steroid 21-hydroxylase deficiency in patients with unilateral and bilateral adrenal incidentalomas. Eur J Endocrinol 147: 349–355.
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