Evidence map›Paper›PMID 35676716›Full record

ArticleWorld journal of surgical oncology2022

Paraganglioma of the urinary bladder initially diagnosed as gastrointestinal stromal tumor requiring combined resection of the rectum: a case report.

Natsumi Matsuzawa, Takeshi Nishikawa, Riki Ohno, Masaharu Inoue, Yu Nishimura, Tomomi Okamoto, Takao Shimizu, Takahide Shinagawa, Yusuke Nishizawa, Shinsuke Kazama

Open access · goldAbstract readCase Reports
In one paragraph

Article in World journal of surgical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Natsumi MatsuzawaDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan. matsuzawa.natsumi@gmail.com.
Takeshi NishikawaDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Riki OhnoDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Masaharu InoueDepartment of Urology, Saitama Cancer Center, Saitama, Japan.
Yu NishimuraDepartment of Pathology, Saitama Cancer Center, Saitama, Japan.
Tomomi OkamotoDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Takao ShimizuDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Takahide ShinagawaDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Yusuke NishizawaDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Shinsuke KazamaDepartment of Gastroenterological Surgery, Saitama Cancer Center, Saitama, 362-0806, Japan.
Saitama Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParaganglioma of the urinary bladder (Pub) is rare and presents with clinical symptoms caused by catecholamine production and release. The typical symptoms of Pub are hypertension, macroscopic hematuria, and a hypertensive crisis during micturition. The average size of detected Pubs is approximately 3 cm. Herein, we report a case of a large Pub in which the symptoms were masked by oral medication, precise preoperative diagnosis was difficult, and intraoperative confirmation of tumoral adhesion to the rectum resulted in hypertensive attacks during surgery. CASE PRESENTATION: A 64-year-old Japanese male with a history of hypertension and arrhythmia controlled with oral medication presented with a large tumor in the pelvic region, detected on examination for weight loss, with no clinical symptoms. Computed tomography and magnetic resonance imaging revealed a tumor measuring 77 mm in diameter in the posterior wall of the urinary bladder. The border with the rectum was unclear, and the tumor showed heterogeneous enhancement in the solid part with an enhancing hypodense lesion. Cystoscopy revealed compression of the bladder trigone by external masses; however, no tumor was visible in the lumen. Endoscopic ultrasonography-guided fine-needle aspiration revealed CD34-positive spindle-shaped cells in the fibrous tissue, suggestive of a mesenchymal neoplasm. The tumor was suspected to be a gastrointestinal stromal tumor, and surgery was performed. After laparotomy, we suspected that the tumor had invaded the rectum, and total cystectomy and anterior resection of the rectum were performed. Histologically, the tumor cells had granular or clear amphophilic cytoplasm with an oval nucleus and nests of cells delimited by connective tissue and vascular septations. Immunohistochemically, the tumor was positive for chromogranin A, CD56, and synaptophysin, and a diagnosis of paraganglioma of the urinary bladder was confirmed. There was no tumor recurrence at the 7-month follow-up.

conclusionThis case highlights the importance of careful examination of pelvic tumors, including endocrine testing, for detecting paraganglioma of the urinary bladder in patients with a history of hypertension or arrhythmia.

Indexed as

Adrenal Gland NeoplasmsGastrointestinal Stromal TumorsHypertensionParagangliomaPheochromocytomaUrinary Bladder NeoplasmsHumansMaleMiddle AgedPelvisRectumUrinary BladderHypertensionLarge pelvic tumorParaganglioma of the urinary bladder

Identifiers

PMID35676716
PMCPMC9178902
OpenAlexW4282926045

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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.