Evidence map›Paper›PMID 41069539›Full record

ArticleActa endocrinologica (Bucharest, Romania : 2005)

A RARE CAUSE OF CUSHING'S SYNDROME: BILATERAL PRIMARY PIGMENTED MICRONODULAR ADRENAL DISEASE.

B Gündüz, S Ç Türk, Y Kayhan, S Çalışkan, I Çamlıdağ, E K Kan, A Atmaca, R Çolak

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In one paragraph

Article in Acta endocrinologica (Bucharest, Romania : 2005). 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

8 authors.

B GündüzOndokuz Mayis University, Faculty of Medicine, Division of Endocrinology and Metabolism, Department of Internal Medicine.
S Ç TürkOndokuz Mayis University, Faculty of Medicine, Division of Endocrinology and Metabolism, Department of Internal Medicine.
Y KayhanOndokuz Mayis University, Faculty of Medicine, Division of Endocrinology and Metabolism, Department of Internal Medicine.
S ÇalışkanOndokuz Mayis University, Faculty of Medicine, Department of Pathology.
I ÇamlıdağOndokuz Mayis University, Faculty of Medicine, Department of Radiology, Samsun, Turkey.
E K KanOndokuz Mayis University, Faculty of Medicine, Division of Endocrinology and Metabolism, Department of Internal Medicine.
A AtmacaOndokuz Mayis University, Faculty of Medicine, Division of Endocrinology and Metabolism, Department of Internal Medicine.
R ÇolakOndokuz Mayis University, Faculty of Medicine, Division of Endocrinology and Metabolism, Department of Internal Medicine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary Pigmented Micronodular Adrenal Disease is a rare cause of Cushing's syndrome, typically observed in children and young adults. It is often associated with the Carney complex. A typical, subclinical, or cyclic Cushing's syndrome clinic can be seen clinically. Treatment options include bilateral-unilateral adrenalectomy or medical treatment. This case presentation aims to draw attention to a rare condition by presenting a patient diagnosed with isolated PPNAD unrelated to the Carney complex.

Indexed as

Cushing’s SyndromehypercortisolemiaPrimary pigmented micronodular adrenal disease

Identifiers

PMID41069539
PMCPMC12506872

What OpenQuestion holds

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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.