Evidence map›Paper›PMID 33150313›Full record

ArticlePediatric investigation2020

Clinical characteristics and prognosis of pulmonary inflammatory myofibroblastic tumor: An over 10-year retrospective analysis.

Na Zhang, Qi Zeng, Chenghao Chen, Jie Yu, Dong Yan, Changqi Xu, Dingyi Liu, Qian Zhang, Xu Zhang

Open access · goldAbstract read
In one paragraph

Article in Pediatric investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  10. Inflammatory Myofibroblastic Tumor: Two Cases in Head and Neck Region.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2022
    Article
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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

9 authors at 2 institutions in 1 country.

Na ZhangDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Qi ZengDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Chenghao ChenDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Jie YuDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Dong YanDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Changqi XuDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Dingyi LiuDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Qian ZhangDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Xu ZhangDepartment of Thoracic Surgery Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Capital Medical University · CNBeijing Children’s Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importancePulmonary inflammatory myofibroblastic tumors (PIMTs) are primary lung tumors in children. Misdiagnosis easily occurs because of the nonspecific clinical manifestations, laboratory examination results, and imaging findings in affected patients.

objectiveTo summarize the clinical characteristics, diagnosis, and prognosis of children with PIMTs.

methodsThis retrospective analysis included 23 children with PIMTs who received treatment in our hospital from January 2008 to January 2019. The clinical manifestations, laboratory examination results, and computed tomography findings were retrospectively analyzed.

resultsThe population included 13 boys and 10 girls, with a median age at onset of 78 months (range, 10-126 months). Fourteen patients had PIMT lesions in the right lung and nine patients had PIMT lesions in the left lung. The surgical procedures included pulmonary wedge resection, pulmonary lobectomy, and total pneumonectomy. The median operation time was 115 min (range, 45-235 min); the median intraoperative blood loss volume was 30 mL (range, 3-500 mL). During the operation, one patient each had pulmonary hemorrhage, vena cava hemorrhage, and thoracic duct injury. Postoperative complications included pulmonary embolism in one patient and tumor recurrence in two patients; neither of these complications recurred after reoperation. The median follow-up period was 49 months (range, 2-127 months).

interpretationChildren with PIMTs exhibited good prognoses and primarily underwent surgical resection as treatment. Complete preoperative evaluation should be performed in affected patients.

Indexed as

ChildrenPulmonary inflammatory myofibroblastic tumorsSurgery

Identifiers

PMID33150313
PMCPMC7520109
OpenAlexW3088910379

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.