Acromegaly in preadolescence: A case report of a 9-year-old boy with acromegaly

Author:

Mbadugha Tobechi1,Ogiwara Toshihiro1,Nagm Alhusain1,Hasegawa Takatoshi1,Kamiya Keisuke1,Matsumoto Yuki2,Kobayashi Mikiko2,Hongo Kazuhiro1

Affiliation:

1. Departments of Neurosurgery, Shinshu University, School of Medicine, Asahi, Matsumoto, Nagano, Japan.

2. Departments of Pathology, Shinshu University, School of Medicine, Asahi, Matsumoto, Nagano, Japan.

Abstract

Background: Acromegaly has been reported in adolescents and young adults, but it is unusual in preadolescence. Diagnosis and management pose different challenges in this age group. Here, we present a rare case of acromegaly in preadolescence. Case Description: A 9-year-old boy presented with acromegalic features and MRI revealed a pituitary tumor. He was diagnosed as having growth hormone secreting pituitary adenoma based on the multidisciplinary assessment, and underwent gross total tumor resection through an endoscopic endonasal approach (EEA) with subsequent normalization of the hormonal parameters. Conclusions: Advances in EEA have made safe removal and cure possible even in children. However, long- term follow-up is needed in such younger patients with multidisciplinary management by neurosurgeons, endocrinologists, pediatricians, and ENT surgeons.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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