Case Report
Copyright ©The Author(s) 2018.
World J Clin Cases. Nov 26, 2018; 6(14): 800-806
Published online Nov 26, 2018. doi: 10.12998/wjcc.v6.i14.800
Table 1 Clinical features of Carney complex and some similar genetic syndromes
Clinical featuresEstimated incidence[7-13]
Carney complexLentigines70%-80%
Blue nevi40%
Cutaneous myxomasLess than 50%
Primary pigmented nodular adrenocortical disease25%-45%
Asymptomatic growth hormone hypersecretion66%
Large cell calcifying Sertoli cell tumors75% of male patients
Thyroid nodules75%
Cardiac myxomas30%-72%
Psammomatous melanotic schwannomas18%
Benign breast tumor14% of female patients
Osteochondromyxomas< 1%
Peutz-Jeghers syndromeMucocutaneous pigmentationMore than 95%
Hamartomatous polypsMost of the patients
McCune-Albright syndromePeripheral precocious puberty50% in females at 4 yr in de Sanctis C’s research
Irregular café-au-lait skin pigmentationAlmost all the patients in de Sanctis C’s research
Fibrous dysplasia of bone50% at 8 yr of age in de Sanctis C’s research