Evidence map›Paper›PMID 39393841›Full record

ArticleAJNR. American journal of neuroradiology2025

Pituitary Gland Duplication Syndrome: An International Imaging Analysis.

Ulrike Löbel, Martin Catala, Felice D'Arco, Maarten H Lequin, Rosa Pasquariello, Pilvi Ilves, Dagmar Loorits, Annika Tähepõld, Giulio Pezzetti, Ian Craven and 2 more

Abstract readMulticenter Study
In one paragraph

Article in AJNR. American journal of neuroradiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Ulrike LöbelFrom the Department of Radiology (U.L., F.D.), Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom ulrike.loebel@gmail.com.ORCID 0000-0001-9844-3464
Martin CatalaLaboratory of Developmental Biology (M.C.), CNRS, Sorbonne-University, IPBS, Paris, France.ORCID 0000-0003-1554-9007
Felice D'ArcoFrom the Department of Radiology (U.L., F.D.), Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
Maarten H LequinDepartment of Radiology (M.H.L.), Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.ORCID 0000-0001-7488-1734
Rosa PasquarielloDepartment of Developmental Neuroscience (R.P.), IRCCS Stella Maris Foundation, Pisa, Italy.
Pilvi IlvesDepartment of Radiology (P.I., D.L., A.T.), Tartu University Hospital, Tartu, Estonia.
Dagmar LooritsDepartment of Radiology (P.I., D.L., A.T.), Tartu University Hospital, Tartu, Estonia.
Annika TähepõldDepartment of Radiology (P.I., D.L., A.T.), Tartu University Hospital, Tartu, Estonia.
Giulio PezzettiUOC Neuroradiologia (G.P.), ASST Papa Giovanni XXIII, Bergamo, Italy.
Ian CravenDepartment of Radiology (I.C.), Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Mariasavina SeverinoNeuroradiology Unit (M.S., A.R.), IRCCS Istituto Giannina Gaslini, Genoa, Italy.ORCID 0000-0003-4730-5322
Andrea RossiNeuroradiology Unit (M.S., A.R.), IRCCS Istituto Giannina Gaslini, Genoa, Italy.ORCID 0000-0001-8575-700X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeDuplication of the pituitary gland is a rare developmental anomaly. Multiple associated craniofacial malformations have previously been reported with the largest series to date consisting of 5 patients. In this multi-institutional series of 10 patients, we present a detailed review of the imaging features and discuss a possible overarching pathogenesis that would explain most of the detected malformations. MATERIALS AND

methodsInclusion criteria for this retrospective imaging review were the presence of a pituitary stalk and gland duplication and the characteristic appearance of the hypothalamic ventral midline. In addition to the clinical presentation, we recorded the imaging findings of 10 patients (9 girls) through onsite and online reviews. Genetic analysis was available for 6 patients.

resultsThe duplicated pituitary stalk and gland showed normal imaging appearances in all patients. Mammillary bodies were clearly identified lateral to the characteristic prominence of the hypothalamic ventral midline. Strands of tissue extending to the anterior dura ("limited ventral myeloschisis") were noted at the medulla oblongata in 10, and at the cervical spinal cord in 7 patients. The medulla oblongata showed a "butterfly" appearance on axial images in 9 patients. Ten patients had cervical segmentation anomalies ("zipperlike"), 9 had anterior-posterior brainstem patterning defects (small pons, elongated medulla), and corpus callosum measurements were abnormal in all patients. Three patients each presented with diencephalic-mesencephalic junction abnormalities and 4 with an anterior mesencephalic "cap." An oropharyngeal teratoma was present in 4 patients. Genetics was normal in 3 of the 6 patients studied; the remainder were found to have mutations in

conclusionsDuplication of the pituitary gland presents as well-defined craniofacial and cervical spine malformation phenotype. Axial mesoderm duplication generating an excess of Sonic Hedgehog may be the primary embryologic driver leading to this condition.

Indexed as

Abnormalities, MultipleMagnetic Resonance ImagingPituitary GlandAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesSyndrome

Identifiers

PMID39393841
PMCPMC11979832

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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.