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Author ORCID Identifier

https://orcid.org/0009-0003-7570-4723

Corresponding Author

TANDURE VARSHA

[email protected]

Abstract

Primary hyperparathyroidism is an endocrine disorder characterized by excessive secretion of parathyroid hormone, most commonly due to a solitary parathyroid adenoma, resulting in hypercalcemia and multisystem involvement [1]. Although many patients are diagnosed incidentally, delayed recognition may lead to severe renal, skeletal, gastrointestinal, and cardiovascular complications.

We report the case of a 44-year-old male who presented with sepsis and acute kidney injury, later found to have hypercalcemia with nephrocalcinosis, chronic calcific pancreatitis, skeletal deformities, and markedly elevated parathyroid hormone levels. Imaging localized a parathyroid adenoma, and the patient underwent successful parathyroidectomy with significant biochemical and clinical improvement.

This case emphasizes the importance of early consideration of primary hyperparathyroidism in patients presenting with unexplained multisystem disease and highlights the reversibility of several complications following timely surgical intervention.

Publication Date

2026

Publisher

JSS Academy of Higher Education & Research

Conflict of Interest

The authors declare no conflict of interest

Keywords

Primary hyperparathyroidism; Parathyroid adenoma; Hypercalcemia; Nephrocalcinosis; Chronic calcific pancreatitis

Word Count

1314

Creative Commons License

Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.

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