Evidence map›Paper›PMID 40860855›Full record

ArticleThe Pan African medical journal2025

[A case report of paraneoplastic Cushing's syndrome in young adults: a rare entity and real diagnostic challenge].

Ghizlane Sabbar, Kaoutar Rifai, Fatima Toulali, Hinde Iraqi, Mohamed El Hassan Gharbi

Abstract readCase ReportsEnglish Abstract
In one paragraph

Article in The Pan African medical journal, 2025. 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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0cells of the map it votes in
0citing papers in PubMed
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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

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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

5 authors.

Ghizlane SabbarService d'Endocrinologie et Maladies Métaboliques, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.
Kaoutar RifaiService d'Endocrinologie et Maladies Métaboliques, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.
Fatima ToulaliService d'Endocrinologie et Maladies Métaboliques, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.
Hinde IraqiService d'Endocrinologie et Maladies Métaboliques, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.
Mohamed El Hassan GharbiService d'Endocrinologie et Maladies Métaboliques, Centre Hospitalier Universitaire Ibn Sina, Rabat, Maroc.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paraneoplastic Cushing's syndrome is a rare cause of ACTH-dependent Cushing's syndrome, rarely observed in young adults, and often presents a challenge in determining its etiology. We report the case of a 16-year-old female patient presenting with a severe hypercortisolism, for which no underlying cause could initially be identified. Her clinical condition worsened, leading to emergency bilateral adrenalectomy as a life-saving measure. The underlying tumor pathology was diagnosed several months later on the basis of functional imaging. The patient underwent surgical excision, resulting in significant clinical improvement. This case highlights both a rare form of ACTH-dependent Cushing's syndrome and the very young age of onset, demonstrating the difficulty in establishing a precise etiological diagnosis, often requiring advanced imaging techniques.

Indexed as

AdrenalectomyCushing SyndromeParaneoplastic SyndromesAdolescentAge of OnsetFemaleHumansbilateral adrenalectomycase reportneuroendocrine tumorsParaneoplastic Cushing's syndromesteroidogenesis inhibitors

Identifiers

PMID40860855
PMCPMC12374737

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Registered trials

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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.