Turner syndrome and Cushing disease - the coexistence with overlapping complications: case report and literature review.
ACTH-Secreting Pituitary Adenoma
/ complications
Adenoma
/ complications
Adult
Diabetes Mellitus, Type 2
/ drug therapy
Estrogen Replacement Therapy
Female
Humans
Myocardial Infarction
/ etiology
Osteoporosis
/ diagnostic imaging
Osteoporotic Fractures
/ etiology
Pituitary ACTH Hypersecretion
/ complications
Turner Syndrome
/ complications
Cushing disease
Turner syndrome
body composition
cardiovascular complications
trabecular bone score
Journal
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
ISSN: 1473-0766
Titre abrégé: Gynecol Endocrinol
Pays: England
ID NLM: 8807913
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
pubmed:
28
6
2019
medline:
11
4
2020
entrez:
28
6
2019
Statut:
ppublish
Résumé
We present an unusual case of Turner syndrome (TS) and Cushing disease (CD) in a young woman, admitted to our department seven years after a successful surgical removal of ACTH-secreting pituitary tumor. To our knowledge, this is the first ever report of these two disorders coexisting. Our patient was diagnosed with TS at the age of 16 due to primary amenorrhea and short stature. Hormone replacement therapy with estrogen was initiated, but she did not receive growth hormone therapy. At the age of 28, she developed clinical and biochemical abnormalities consistent with hypercortisolism, but the definitive diagnosis of CD was established nine years later when she was admitted to our department. Appropriate treatment was applied, however, the patient developed serious complications: a myocardial infarction, diabetes and osteoporosis. Surgical treatment appeared to improve some, but not all of the symptoms, indicating a significant contribution of concomitant TS to the severity of adverse cardiovascular and bone turnover outcomes in a subject with a genetic susceptibility to these complications. Thus, multidisciplinary evaluation in such patients is strongly indicated, particularly if more predisposing conditions are present.
Identifiants
pubmed: 31242778
doi: 10.1080/09513590.2019.1631281
doi:
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM