Evidence map›Paper›PMID 40709295›Full record

ArticleJournal of clinical imaging science2025

Partially calcified giant hemorrhagic syringomyelia and hematomyelia.

Adnan Duriqi, Kreshnike Dedushi Hoti, Kaltrina Gocaj, Fjolla Hyseni

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical imaging science, 2025. 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

4 authors.

Adnan DuriqiUniversity Clinical Center of Kosova, Euromed Hospital, Fushe Kosove, Prishtine, Kosovo, Albania.
Kreshnike Dedushi HotiDepartment of Radiology, Faculty of Medicine, University of Prishtina "Hasan Prishtina", Prishtine, Kosovo, Albania.
Kaltrina GocajDepartment of Radiology, University Clinical Center of Kosova, Prishtine, Kosovo, Albania.
Fjolla HyseniDepartment of Spine Surgery, Clinic of Orthopedics, Department of Pediatrics, New York University, Port Chester, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Syringomyelia is a rare condition characterized by the formation of a fluid-filled cyst within the spinal cord, leading to myelopathy. In addition, the pathological enlargement of the central canal is referred to as hydromyelia or cleft-like syrinx. We present a case of idiopathic syringomyelia and hematomyelia in a 50-year-old female patient with a 5-year follow-up on her disease progression. Magnetic resonance imaging (MRI) images revealed low-signal intensity on T1 and high-signal intensity on T2, with elevated hemorrhagic signal intensity on T1 and low peripheral signal intensity on T2. A fluid-filled lesion measuring 12 × 36 mm was observed between the C7 and Th3 vertebrae, with separation from some of the detailed components. No contrast enhancement was noted following IV contrast administration. Based on the MRI findings, a diagnosis consistent with giant hemorrhagic syringomyelia was established. Subsequently, a neurosurgical intervention was performed, resulting in a reduction in the size of the syringomyelia and a moderate improvement in the patient's symptom profile.

Indexed as

Giant hemorrhagic syringomyeliaHematomyeliaMagnetic resonance imagingSyringomyelia

Identifiers

PMID40709295
PMCPMC12289104

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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.