Evidence map›Paper›PMID 42257228›Full record

ArticleCase reports in transplantation2026

Spindle Cell Sarcoma of the Abdominal Aorta Following Endovascular Aneurysm Repair in a Kidney Transplant Recipient.

Kota Kakeshita, Teruhiko Imamura, Hidenori Yamazaki, Kanetsugu Nagao, Shigeyuki Yamashita, Shinya Kajiura, Naotaka Nishiyama, Noriko Okuno, Tsutomu Koike, Hiroshi Kitamura and 1 more

Abstract read
In one paragraph

Article in Case reports in transplantation, 2026. 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

11 authors.

Kota KakeshitaThe Second Department of Internal Medicine, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0003-0164-8290
Teruhiko ImamuraThe Second Department of Internal Medicine, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0002-7294-7637
Hidenori YamazakiThe Second Department of Internal Medicine, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0002-4974-4356
Kanetsugu NagaoThe First Department of Surgery, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0009-0007-2651-4463
Shigeyuki YamashitaThe First Department of Surgery, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0002-4784-736X
Shinya KajiuraDepartment of Medical Oncology and Palliative Medicine, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0003-4920-5130
Naotaka NishiyamaDepartment of Urology, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0003-2017-2312
Noriko OkunoDepartment of Pathology, University of Toyama, Toyama, Japan, u-toyama.ac.jp.
Tsutomu KoikeThe Second Department of Internal Medicine, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0009-0002-5912-1870
Hiroshi KitamuraDepartment of Urology, University of Toyama, Toyama, Japan, u-toyama.ac.jp.
Koichiro KinugawaThe Second Department of Internal Medicine, University of Toyama, Toyama, Japan, u-toyama.ac.jp.ORCID https://orcid.org/0000-0003-0009-8477

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A kidney transplant recipient developed spindle cell sarcoma within an abdominal aortic aneurysm following prior endovascular aneurysm repair (EVAR). The patient had undergone EVAR for abdominal aortic aneurysm before successful living-donor kidney transplantation and maintained stable graft function under immunosuppressive therapy. Two years after transplantation, he presented with back pain, elevated inflammatory marker, and aneurysm enlargement, initially suspected as an infected aneurysm. Despite antibiotic therapy, the lesion progressed. Positron emission tomography demonstrated increased fluorodeoxyglucose uptake, and computed tomography-guided biopsy revealed undifferentiated spindle cell sarcoma with unclear lineage differentiation. Surgical resection was not feasible, and systemic chemotherapy was initiated; however, disease progression continued, and the patient died 7 months after admission. Aortic sarcoma following EVAR is rare and may mimic infection or inflammatory complications. Clinicians should consider malignant etiologies when transplant recipients with prior EVAR present with atypical aneurysm enlargement or persistent inflammatory findings, and early tissue diagnosis may be necessary.

Indexed as

abdominal aortic aneurysmEVARimmunosuppressioninfected aneurysmposttransplant malignancysoft tissue sarcoma

Identifiers

PMID42257228
PMCPMC13238242

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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.