When a Patient’s Relative Becomes the Patient: An Incidental Diagnosis of Acromegaly

Bangladesh Journal of Endocrinology and Metabolism 2026 Open access

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Authors: Kabiru Bello Sada, Aisha Mohemmed, Kabiru Mande Mohammed, Umar Abdullahi, Mohammad Kaura Abubakar, Y. A. Sikiru
DOI: 10.4103/bjem.bjem_40_25
Cited by: 0
References: 8

Abstract

A bstract Acromegaly is a rare endocrine disorder caused by excessive secretion of growth hormone and insulin-like growth factor-1, most commonly due to a pituitary adenoma. The condition develops insidiously and is often diagnosed late after years of progressive somatic and metabolic changes. This case report presents an unusual case of a middle-aged man incidentally diagnosed with acromegaly while accompanying his mother to the clinic for a routine medical checkup. The case report highlights the clinical features, diagnostic approach, management, and prognosis of this uncommon condition.

Fields of Study & Subjects

Pituitary Gland Disorders and Treatments Growth Hormone and Insulin-like Growth Factors Neuroendocrine Tumor Research Advances

Publication details

Journal / source
Bangladesh Journal of Endocrinology and Metabolism
Volume
5
Issue
2
Pages
210–212
Publication date
10 March 2026
Language
EN