Case Report

Rare Case of Parathyroid Adenoma Diagnosed in 18 Year Old YoungMale Patient

Faizan Banaras
Allied Ayub Teaching Hospital Abbottabad, KPK
Ali Raza
Allied Ayub Teaching Hospital Abbottabad, KPK
Saifuddin Saifuddin
Allied Ayub Teaching Hospital Abbottabad, KPK
Qaiser Ali
Allied Ayub Teaching Hospital Abbottabad, KPK
Abdul Ali
Allied Ayub Teaching Hospital Abbottabad, KPK
Dilawer Khan
Allied Ayub Teaching Hospital Abbottabad, KPK

✉ Correspondence: Faizan Banaras Email: faizanbanaras958@gmail.com

DOI https://doi.org/10.70302/jpsim.v4i2.2331
Volume: 4, Issue 2 Pages: 149–151 Published: 02 Jun 2023
Received: 02 Feb 2023 Accepted: 02 Apr 2023 Published Online: 02 Jun 2023

Abstract

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.

Keywords
Parathyroid Adenoma Diagnosis Endocrine Neoplasia.

How to Cite This Article

Banaras F, Raza A, Saifuddin S, Ali Q, Ali A, Khan D. Rare Case of Parathyroid Adenoma Diagnosed in 18 Year Old YoungMale Patient. J Pak Soc Intern Med. 2023;4(2):149–151. doi:10.70302/jpsim.v4i2.2331

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Conflict of Interest

All authors declare no competing interests.

Disclosed in accordance with ICMJE and COPE guidelines.

Funding

No specific funding was received for this research.

Funder information follows the Crossref Funder Registry standard.

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Reference list indexed for Google Scholar and ResearchGate. DOI links resolve via doi.org.

CC BY CC BY 4.0 This article is published under the Creative Commons Attribution 4.0 International License. May be shared and adapted with attribution. © 2023 Journal of Pakistan Society of Internal Medicine.
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