ACTH ectopic syndrome caused by corticomedullary mixed tumor | Zendy

Evgeniya Marova | Zendy; Н С Кузнецов | Zendy; Liudmila Rozhinskaya | Zendy; О. В. Ремизов | Zendy; Н В Латкина | Zendy; Olga V. Tikhonova | Zendy; Lyubov Efimovna Kats | Zendy; Iya Aleksandrovna Voronkova | Zendy; А. М. Лапшина | Zendy; Г. С. Колесникова | Zendy

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ACTH ectopic syndrome caused by corticomedullary mixed tumor

Author(s) -

Evgeniya Marova,

Н С Кузнецов,

Liudmila Rozhinskaya,

О. В. Ремизов,

Н В Латкина,

Olga V. Tikhonova,

Lyubov Efimovna Kats,

Iya Aleksandrovna Voronkova,

А. М. Лапшина,

Г. С. Колесникова

Publication year - 2016

Publication title -

problems of endocrinology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.124

H-Index - 5

eISSN - 2308-1430

pISSN - 0375-9660

DOI - 10.14341/probl201662150-54

Subject(s) - medicine , pathology , pheochromocytoma , endocrinology

We report the case of a 61 year old woman with a typical clinical picture of ACTH dependent Cushing’s syndrome. Diagnostic tests confirmed ACTH dependent Cushing’s syndrome, which is caused by corticomedullary mixed tumor. ACTH-secreting pheochromocytoma are rarely described in accessible literature, there is no one case report about ACTH-secreting corticomedullary mixed tumor. Due to the rarity of the disease, we believe it appropriate to share our experience and consider all variants of interaction in hypothalamic-pituitary-adrenal axis, which could lead to morphology and clinical changes uncovered in this case.

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