hrp0098p3-2 | Adrenals and HPA Axis | ESPE2024

A case of suspected Pigmented primary nodular adrenocortical disease with a Tanner stage inconsistent with testosterone levels

Tanimoto Eri , Nakamura Chizuko , Ishimaru Masanori , Fukui Sadahiro , Miyagi Hajime , Ujita Nagisa , Doi Hibiki , Igarashi Mizuho , Kashima Takemoto , Yoneda Akhiro , Matsubara Keiko , Shima Hirohito , Kannno Jyunko , Yoshii Keisuke , Naiki Yasuhiro , Horikawa Reiko

Background: Adrenal tumour in childhood is relatively rare, and its clinical features are variable depending on hormonal profiles. Pigmented primary nodular adrenocortical disease (PPNAD) and adrenal carcinoma may present with clinical signs of precocious puberty due to increased adrenal androgen secretion in addition to glucocorticoids. [Case] 12-year-old boy. Obesity and short stature were noted on school health check-up a year ago. The endocrinological work...