Evidence map›Paper›PMID 42504276›Full record

ArticleJCEM case reports2026

A challenging diagnosis of pediatric (cyclic) Cushing disease: the decisive role of hair cortisol.

Lizanne Berkenbosch, Saartje Straetemans

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Lizanne BerkenboschPediatric Endocrinology, MosaKids Children's Hospital, MUMC+, 6229 HX Maastricht, The Netherlands.ORCID https://orcid.org/0009-0004-1694-2833
Saartje StraetemansPediatric Endocrinology, MosaKids Children's Hospital, MUMC+, 6229 HX Maastricht, The Netherlands.ORCID https://orcid.org/0000-0001-7857-3608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cushing disease is a rare and often difficult diagnosis. Therefore, a significant delay between the onset of symptoms and the final diagnosis frequently occurs. We present a previously healthy 12-year-old boy in whom hypercortisolism was suspected based on clinical symptoms: abrupt excessive weight gain despite adequate exercise and dietary interventions in combination with growth arrest. The results of conventional biochemical diagnostics for Cushing disease were contradicting and could not confirm the diagnosis. Because of a persistent clinical suspicion after a wait-and-see period, cortisol levels in the boy's 11 cm long hair were analyzed. The very high hair cortisol levels supported the clinically suspected Cushing disease. Magnetic resonance imaging of the pituitary showed evidence of an adenoma, which was confirmed postoperatively as an adrenocorticotropic hormone producing adenoma. This confirmed the diagnosis of Cushing disease, with most likely a cyclical course, 1.5 years after the initial presentation. This case adds to the scarce literature on pediatric cyclic Cushing disease and emphasizes the added value of hair cortisol.

Indexed as

childCushing diseasehair cortisol

Identifiers

PMID42504276
PMCPMC13402041

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.