Adrenal cytomegaly with elevated serum androgen levels in a patient with Beckwith-Wiedemann syndrome
Author:
Affiliation:
1. Department of Pediatrics, Nihon University School of Medicine, Tokyo, Japan
2. Department of Pediatric Surgery, Nihon University School of Medicine, Tokyo, Japan
3. Department of Pathology, Nihon University School of Medicine, Tokyo, Japan
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.jstage.jst.go.jp/article/endocrj/69/8/69_EJ21-0261/_pdf
Reference23 articles.
1. 1 MacFarland SP, Mostoufi-Moab S, Zelley K, Mattei PA, States LJ, et al. (2017) Management of adrenal masses in patients with Beckwith-Wiedemann syndrome. Pediatr Blood Cancer 64: 10.1002/pbc.26432.
2. 2 Rump P, Zeegers MP, van Essen AJ (2005) Tumor risk in Beckwith-Wiedemann syndrome: a review and meta-analysis. Am J Med Genet A 136: 95–104.
3. 3 Allolio B, Fassnacht M (2006) Clinical review: adrenocortical carcinoma: clinical update. J Clin Endocrinol Metab 91: 2027–2037.
4. 4 Mendonca BB, Lucon AM, Menezes CA, Saldanha LB, Latronico AC, et al. (1995) Clinical, hormonal and pathological findings in a comparative study of adrenocortical neoplasms in childhood and adulthood. J Urol 154: 2004–2009.
5. 5 Noguchi S, Masumoto K, Taguchi T, Takahashi Y, Tsuneyoshi M, et al. (2003) Adrenal cytomegaly: two cases detected by prenatal diagnosis. Asian J Surg 26: 234–236.
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