Carney Complex Complicated with Primary Pigmented Nodular Adrenocortical Disease without Cushing's Syndrome Recurrence for Five Years after Unilateral Adrenalectomy
Author:
Affiliation:
1. Endocrinology and Diabetes Center, Yokohama Rosai Hospital, Japan
2. Division of Endocrinology and Metabolism, Kanto Central Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/61/2/61_7418-21/_pdf
Reference19 articles.
1. 1. Kirschner LS, Carney JA, Pack SD, et al. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet 26: 88-92, 2000.
2. 2. Stratakis CA, Carney JA, Lin JP, et al. Carney complex, a familial multiple neoplasia and lentiginosis syndrome: analysis of 11 kindreds and linkage to the short arm of chromosome 2. J Clin Invest 97: 699-705, 1996.
3. 3. Stratakis CA, Kirschner LS, Carney JA. Clinical and molecular features of the carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab 86: 4041-4046, 2001.
4. 4. Powell AC, Stratakis CA, Patronas NJ, et al. Operative management of Cushing syndrome secondary to micronodular adrenal hyperplasia. Surgery 143: 750-758, 2008.
5. 5. Ritzel K, Beuschlein F, Mickisch A, et al. Outcome of bilateral adrenalectomy in Cushing's syndrome: a systematic review. J Clin Endocrinol Metab 98: 3939-3948, 2013.
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1. From cortisol-producing adrenal adenoma to atrial myxoma, through nivolumab-induced hypophysitis: a complicated case report of Carney Complex;Endocrine;2024-09-01
2. The clinical characteristics and pathogenic variants of primary pigmented nodular adrenocortical disease in 210 patients: a systematic review;Frontiers in Endocrinology;2024-06-26
3. Carney complex- why thorough medical history taking is so important - report of three cases and review of the literature;Endocrine;2022-10-18
4. Phenotypic Variability in a Family with Carney Complex Accompanied by a Novel Mutation Involving <i>PRKAR1A</i>;The Tohoku Journal of Experimental Medicine;2022
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