ESPE Abstracts (2021) 94 P2-343

ESPE2021 ePoster Category 2 Multisystem endocrine disorders (13 abstracts)

Autoimmune polyendocrine syndrome type 2 and precocious puberty: a rare association

Imane Assarrar 1,2 , Najoua Messaoudi 1,2 , Siham Benouda 1,2 , Siham Rouf 1,2 & Hanane Latrech 1,2


1Department of Diabetology-Endocrinology and Nutrition, Mohammed VI University Hospital Center, Oujda, Morocco; 2Medical School, Mohamed the First University, Oujda, Morocco


Introduction: Precocious puberty is a common problem affecting up to 29 per 100,000 girls per year. It is defined as the development of secondary sexual features, at a younger age than the accepted lower limits for age of onset of puberty, namely 8 years in girls and 9.5years in boys. We report the case of a precocious puberty in an 8-year-old and 11months girl with diabetes mellitus type 1 and autoimmune hypothyroidism followed-up in the department of Endocrinology-Diabetology-Nutrition of Mohammed-VI University Hospital Center, Oujda, in the eastern of Morocco.

Case report: An 8-year-old and 11months girl was admitted for the first time to our department for unbalanced diabetes type 1 that was discovered at the age of 5years, for which she was put on basal bolus insulin regimen. The physical examination at admission revealed a breast development stage III according to Tanner staging and a development of pubic hair stage II. The age of onset of secondary sexual characteristics was around 8years; unfortunately the parents were not alarmed and didn’t consult earlier. The young girl had an advanced height at +1SD (standard deviation) with a bone age of 8years and 6months. The patient underwent gonadotropin-releasing hormone (GnRH) stimulation test that revealed a peak luteinizing hormone (LH) concentration at 6,47 mUI/ml. Pituitary magnetic resonance imaging (MRI) was normal. Therefore, the diagnosis of idiopathic central precocious puberty was confirmed. Nonetheless, since the patient had a normal growth velocity and a comforting bone age, GnRH agonists were not used. Furthermore, the screening for autimmune diseases in the patient revealed positive thyroid peroxidase antibodies (TPO antibodies) at 38,47UI/ml (normal range < 34 UI/ml). The young patient developed hypothyroidism 2months later and was put on substitutive hormone therapy. During a regular follow-up of one year, the patient had a sustained normal growth velocity.

Discussion-conclusion: A review of literature of puberty in girls with diabetes type 1 concluded that the age of onset of puberty in young girls with diabetes mellitus type 1 seem to be within normal limits, however some patient experience pubertal delay due to poor glycemic control [1]. Our patient presented with a precocious puberty, this association with autoimmune polyendocrine syndrome type 2 has never been described before. Further investigations are necessary in order to comprehend the particularities of this unusual association.

[1] Codner E, Cassorla F. Puberty and ovarian function in girls with type 1 diabetes mellitus. Horm Res. janv 2009;71(1): 12 21.

Volume 94

59th Annual ESPE (ESPE 2021 Online)

Online,
22 Sep 2021 - 26 Sep 2021

European Society for Paediatric Endocrinology 

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