Cushing syndrome as a failed cardiac screen in a patient with McCune-Albright syndrome: a case report

被引:1
|
作者
Foster, Christy [1 ]
Al Zubeidi, Hiba [2 ]
Diaz-Thomas, Alicia [2 ]
机构
[1] Univ Alabama Birmingham, Dept Pediat, Div Endocrinol, 1601 4th Ave South, Birmingham, AL 35233 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Pediat, Div Endocrinol, Memphis, TN 38163 USA
关键词
Cushing syndrome; Cardiac hypertrophy; McCune-Albright syndrome; CONGENITAL HEART-DISEASE; STIMULATORY G-PROTEIN; ACTIVATING MUTATIONS; ENDOCRINE;
D O I
10.1186/s13256-022-03533-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background McCune-Albright syndrome is a complex disorder encompassing multiple endocrinopathies. These manifestations are secondary to a mutation in the stimulatory G-protein alpha subunit. Cushing syndrome is due to autonomous secretory function of the adrenal gland and is present in 7.1% of patients with McCune-Albright syndrome. Cardiac newborn screenings assist in the identification of critical congenital heart disease. These screenings have become part of routine postnatal care nationwide. Case report A 6-week-old Caucasian male presented to a cardiologist at the University of Tennessee Health Science Center with left ventricular hypertrophy and poor feeding after a failed cardiac newborn screen. He had been previously seen at 2 weeks by a cardiologist on follow-up for abnormal critical congenital heart disease screening. Electrocardiogram and echocardiographic studies identified hypertrophic cardiomyopathy. Other examination findings revealed multiple characteristic cafe-au-lait lesions along with hypotonia and rounded facies. Given his cardiac disease, he was admitted to the hospital, where an evaluation was done for Cushing syndrome, showing elevated cortisol by immunoassay of 38 mu g/dL (1.7-14.0 mu g/dL, Vitros 5600) after a dexamethasone suppression test and urinary cortisol elevated to 35 mu g/dL/24 hours (reference range 3-9 mu g/dL/24 hours) (Esoterix; Calabasas, CA). He was started on metyrapone therapy to block synthesis of cortisol. His cortisol improved and was suppressed less than 2 mu g/dL. His hypertension and clinical features of Cushing syndrome improved. Conclusions This case demonstrates a unique presentation of Cushing syndrome in a young infant. This is the first case to our knowledge showing significant left ventricular hypertrophy resulting from Cushing syndrome identified following a failure on a critical congenital heart disease screen. It highlights the importance of considering of McCune-Albright syndrome in patients with Cushing syndrome, especially if other clinical features are present. Medical therapy can be used to treat Cushing syndrome and can result in improvement in the cardiovascular pathology.
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页数:5
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