# The unexpected diagnosis of karyomegalic interstitial nephritis in a presumed case of Mesoamerican Nephropathy: a case report

**Authors:** Lawrence Kwon, Jennifer Griffiths, Lanny T. DiFranza

PMC · DOI: 10.3389/fmed.2025.1465783 · Frontiers in Medicine · 2025-03-05

## TL;DR

A farmer in Guatemala was diagnosed with a rare kidney disease instead of a more common one, highlighting the need for thorough evaluations in kidney disease cases.

## Contribution

This case report highlights the importance of considering Karyomegalic Interstitial Nephritis in regions where Mesoamerican Nephropathy is prevalent.

## Key findings

- A kidney biopsy confirmed Karyomegalic Interstitial Nephritis in a patient initially suspected of having Mesoamerican Nephropathy.
- The case emphasizes the need for comprehensive diagnostic evaluation in atypical kidney disease presentations.
- KIN was identified as a distinct condition separate from CKDu in this patient.

## Abstract

Chronic kidney disease of unknown etiology (CKDu) is a form of chronic kidney disease commonly found in certain rural populations globally. This condition is characterized by chronic tubulointerstitial nephropathy, yet it lacks specific signature lesions and is believed to have a multifactorial etiology, often associated with environmental toxins. Karyomegalic Interstitial Nephritis (KIN), although a rare form of chronic interstitial nephropathy leading to end-stage kidney disease, is not classified under CKDu.

In this case report, we explore the diagnostic journey of a 40-year-old male farmer from Guatemala. He presented with headache, fever, and facial pain, but laboratory tests revealed significant kidney impairment and liver dysfunction. The pivotal point in his diagnostic workup was a kidney biopsy, which showed severe chronic tubulointerstitial scarring and enlarged, hyperchromatic nuclei in the tubular epithelial cells, confirming KIN. This diagnosis marked a departure from the initial suspicion of Mesoamerican Nephropathy (MEN).

This case underscores the critical need for a comprehensive evaluation in atypical presentations of chronic kidney disease, particularly emphasizing the importance of being vigilant for KIN in areas where MEN is commonly diagnosed.

## Linked entities

- **Diseases:** chronic kidney disease (MONDO:0005300), Karyomegalic Interstitial Nephritis (MONDO:0013898)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** headache (MESH:D006261), Chronic kidney disease (MESH:D051436), fever (MESH:D005334), facial pain (MESH:D005157), interstitial nephropathy (MESH:D007674), liver dysfunction (MESH:D017093), KIN (OMIM:614817), MEN (MESH:D000092702), end-stage kidney disease (MESH:D007676)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11920115/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC11920115/full.md

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Source: https://tomesphere.com/paper/PMC11920115