Evidence map›Paper›PMID 41048684›Full record

ArticleAACE endocrinology and diabetes

Cushing Disease Mimicking Ectopic Adrenocorticotropic Hormone-Secreting Disease.

David Louis Fisher, Merav Fraenkel, Lior Baraf

Abstract readCase Reports
In one paragraph

Article in AACE endocrinology and diabetes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

3 authors.

David Louis FisherEndocrinology Department, Soroka University Medical Center, Beer Sheva, Israel.
Merav FraenkelEndocrinology Department, Soroka University Medical Center, Beer Sheva, Israel.
Lior BarafEndocrinology Department, Soroka University Medical Center, Beer Sheva, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objective: We present the case of a patient whose initial biochemical results suggested an ectopic adrenocorticotropic hormone (ACTH)-secreting tumor, with markedly increased serum ACTH levels, increased 24-hour urinary free cortisol levels, and hypokalemia. Although these features are more commonly associated with ectopic ACTH secretion, the patient was ultimately diagnosed with Cushing disease. Case Report: A 46-year-old man presented with recurrent headaches and progressive skin darkening. He had hypertension and a body mass index of 28.4 kg/m Discussion: Higher urinary and plasma cortisol levels are typical of ectopic ACTH-secreting tumors and likely cause hypokalemia and hypertension, which are encountered more frequently in patients with ectopic ACTH-secreting tumors. In the absence of a pituitary mass 1 cm or more in size, further testing to differentiate Cushing disease from an ectopic source is required. Conclusion: Highly increased serum ACTH and cortisol levels, hypokalemia, and hypertension occur more frequently in patients with ectopic ACTH-secreting tumors. However, we show that they may occur in Cushing disease, and therefore, it would be wrong to assume a diagnosis of an ectopic ACTH-secreting tumor based on these findings alone.

Indexed as

Cushing diseaseCushing syndromeectopic ACTH-secreting tumor

Identifiers

PMID41048684
PMCPMC12495582

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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.