Vol 71, No 3 (2020)
Clinical vignette
Published online: 2020-03-26

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Corticotropinoma as the underlying cause of intermittent Cushing’s syndrome in a patient previously diagnosed with primary pigmented nodular adrenocortical disease

Agnieszka Łebek-Szatańska1, Maria Stelmachowska-Banaś1, Grzegorz Zieliński2, Andrzej Styk2, Karolina M. Nowak1, Lucyna Papierska1
Pubmed: 32293705
Endokrynol Pol 2020;71(3):273-274.

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References

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  2. Kiefer FW, Winhofer Y, Iacovazzo D, et al. mutation causing pituitary-dependent Cushing disease in a patient with Carney complex. Eur J Endocrinol. 2017; 177(2): K7–KK12.
  3. Hernández-Ramírez LC, Tatsi C, Lodish MB, et al. Corticotropinoma as a Component of Carney Complex. J Endocr Soc. 2017; 1(7): 918–925.
  4. Sarlis NJ, Chrousos GP, Doppman JL, et al. Primary pigmented nodular adrenocortical disease: reevaluation of a patient with carney complex 27 years after unilateral adrenalectomy. J Clin Endocrinol Metab. 1997; 82(4): 1274–1278.