# Pseudohyperkalemia as a New Insight Into the Causes of Hyperkalemia Associated With Atopic Dermatitis

**Authors:** Atsuhiro Yae, Junji Azuma, Eri Kijima, Takehisa Yamamoto, Yasuhiro Hasegawa

PMC · DOI: 10.7759/cureus.79943 · Cureus · 2025-03-03

## TL;DR

A case of pseudohyperkalemia in a child with severe atopic dermatitis is reported, showing that high serum potassium levels were not real and resolved with treatment.

## Contribution

This is the first documented case linking pseudohyperkalemia to atopic dermatitis.

## Key findings

- A 9-month-old girl with severe AD had pseudohyperkalemia due to thrombocytosis.
- Whole-blood potassium levels were normal despite high serum potassium.
- Pseudohyperkalemia resolved after AD treatment and platelet count decreased.

## Abstract

Pseudohyperkalemia is defined as a falsely elevated serum potassium level caused by the release of potassium from blood cells during the clotting process, which occurs in vitro. Although hyperkalemia, a potentially life-threatening condition, has been associated with severe atopic dermatitis (AD) through mechanisms such as the 'aldosterone paradox,' pseudohyperkalemia has not been documented in AD. We present a case of pseudohyperkalemia in a nine-month-old girl with thrombocytosis associated with severe AD. Despite a serum potassium level of 7.3 mEq/L, the whole-blood potassium measured using a blood gas analyzer was 4.8 mEq/L. Therefore, we diagnosed the case as pseudohyperkalemia and decided not to treat the serum hyperkalemia. Following treatment with topical steroids and a Janus kinase inhibitor, the pseudohyperkalemia resolved as the skin condition improved and the platelet count decreased.

## Linked entities

- **Diseases:** atopic dermatitis (MONDO:0004980)

## Full-text entities

- **Diseases:** Pseudohyperkalemia (MESH:C563785), AD (MESH:D003876), Hyperkalemia (MESH:D006947), thrombocytosis (MESH:D013922)
- **Chemicals:** steroids (MESH:D013256), potassium (MESH:D011188), aldosterone (MESH:D000450)

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC11966362/full.md

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Source: https://tomesphere.com/paper/PMC11966362