JPSIM Journal of Pakistan Society of Internal Medicine J Pak Soc Intern Med 2709-8729 2710-0804 Pakistan Society of Internal Medicine 10.70302/jpsim.v4i2.2331 jpsim.v4i2.2331 Case Report Rare Case of Parathyroid Adenoma Diagnosed in 18 Year Old Young Male Patient Banaras Faizan faizanbanaras958@gmail.com * Raza Ali Saifuddin Ali Qaiser Ali Abdul Khan Dilawer Allied Ayub Teaching Hospital Abbottabad, KPK *Correspondence: Faizan Banaras (faizanbanaras958@gmail.com) 02 06 2023 2023 4 2 149 151 02 02 2023 02 04 2023 Copyright © 2023 The Author(s) 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Multiple endocrine neoplasia type 1 (MEN1, wermer's syndrome) is an uncommon autosomal dominant hereditary syndrome characterized by neoplasia of the parathyroid gland, pituitary gland, and pancreas. The parathyroid adenomas are usually not perceptible or conspicuous from much clinical point of view.All the signs and symptoms are mainly because by disturbed serum calcium levels. Calcium has a crucial role in controlling most body functions. The major features of hypercalcemia are renal stones, abdominal groans, bone pain, psychic moans, and fatigue overtones. Parathyroid adenoma has magnificent outcomes by surgical intervention.

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