Evidence map›Paper›PMID 41117981›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

A rare case: solitary fibrous tumor with widespread metastasis on [

Burcin Karasah Erkek, Hatice Sariyildiz Gumusgoz, Ozgur Sanli

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2026. 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

3 authors.

Burcin Karasah ErkekDepartment of Nuclear Medicine, Ege University Faculty of Medicine, Izmir, Turkey. burcinkarasah94@gmail.com.ORCID 0000-0002-4972-0936
Hatice Sariyildiz GumusgozDepartment of Nuclear Medicine, Sakarya Education and Research Hospital, Sakarya, Turkey.
Ozgur SanliDepartment of Nuclear Medicine, Izmir University of Economics Medicalpoint Hospital, Izmir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Intracranial solitary fibrous tumor (SFT) are rare pericyte neoplasms arising from the meninges. They resemble meningiomas due to their location and are hyperdense on CT. Therefore, they may be a source of pitfalls. However, unlike meningiomas, there is no calcification or hyperostosis of the adjacent bone. We report a rare case of metastatic SFT presenting with masses in the left cerebral hemisphere, both lungs, left kidney, C4 vertebra, and scalp with intense radiotracer uptake. Case presentation A 66-year-old male patient was referred to our center with intracranial masses initially diagnosed as meningiomas. The patient, who developed compression symptoms, underwent surgery for masses in the left cerebral hemisphere. According to WHO classification [1], the pathology revealed as high-risk (grade 3) SFT with high proliferative activity. Immunohistochemical findings: Bcl-2-124 (positive), CD34 (focal pale positive), CD99 (membranous positive), Ki67 (MIB1): %14, PHH3 (positive in 10 cells in per 10 high-power fields), STAT 6 (diffuse nuclear positive). And 10 mitoses were seen in per 10 high-power fields. Imaging results revealed extracranial metastases in addition to intracranial masses, both demonstrating intense radiotracer uptake. Conclusions Although SFTs can be confused with meningiomas based on imaging findings, distinguishing between the two is crucial due to the rarity, aggressive behavior, and potential for extracranial metastasis associated with SFTs. Ga-68 DOTA PET/CT offers significant contributions to the differential diagnosis of these two tumor types. However, it is known in the literature that meningiomas can also exhibit a high rate of DOTA uptake, and, although rare, extracranial metastases can exhibit DOTA positivity. Therefore, a holistic approach to evaluating radiologic, clinical, and histopathologic findings is necessary for definitive diagnosis, rather than relying solely on Ga-68 DOTA PET/CT findings. Furthermore, as seen in this rare case with limited therapeutic options, the high expression of somatostatin receptor raises the possibility of radiolabeled somatostatin analogs as a potential treatment option in the context of widespread metastatic disease.

Indexed as

Organometallic CompoundsPositron Emission Tomography Computed TomographySolitary Fibrous TumorsAgedHumansMaleNeoplasm Metastasisgallium Ga 68 dotatateOrganometallic Compounds

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.