Evidence map›Paper›PMID 29535991›Full record

ArticleFrontiers in pediatrics2018

Pulmonary Inflammatory Myofibroblastic Tumor in Children: A Case Report and Brief Review of Literature.

Federica Camela, Marcella Gallucci, Emanuela di Palmo, Salvatore Cazzato, Mario Lima, Giampaolo Ricci, Andrea Pession

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2018. 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
2.4field-weighted citation impact, top 12% 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, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Spindle cell myofibroblastic tumour of bronchus.Lung India : official organ of Indian Chest Society · 2024
    Article
  6. Pulmonary Inflammatory Myofibroblastic Tumor: A Case Report.European journal of pediatric surgery reports · 2024
    Article
  7. Article
  8. Article
  9. Giant lung tumor in hereditary spherocytosis: inflammatory myofibroblastic tumor.Indian journal of thoracic and cardiovascular surgery · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. 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

7 authors at 2 institutions in 1 country.

Federica CamelaDepartment of Pediatrics, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Marcella GallucciDepartment of Pediatrics, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Emanuela di PalmoDepartment of Pediatrics, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Salvatore CazzatoDepartment of Mother and Child Health, Salesi Children's Hospital, Ancona, Italy.
Mario LimaDepartment of Pediatric Surgery, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Giampaolo RicciDepartment of Pediatrics, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Andrea PessionDepartment of Pediatrics, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
University of Bologna · ITPoliclinico S.Orsola-Malpighi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inflammatory myofibroblastic tumor (IMT) is a rare lesion of unclear etiology and variable clinical course, consisting of a proliferation of fibroblasts and myofibroblasts, mixed with inflammatory cells. Synonyms of IMT are inflammatory pseudotumor and plasma cell granuloma reflecting the alleged inflammatory nature attributed to this lesion, even though this heterogeneity in the disease denomination is probably involved in a dispersion of the literature data. Among primary pulmonary neoplasms, it represents the most frequent endobronchial tumor of childhood and beyond the lung it has been described mainly in the bladder, mediastinum and mesentery. Despite having a tendency for local recurrence, the risk of distant metastasis is low. Clinical presentation depends on localization therefore lung peripheral lesions are often asymptomatic resulting in a delayed diagnosis. Radiological findings can suggest the diagnosis that must be confirmed by histopathology assessment. The tumor has been characterized by the application of immunohistochemical techniques, molecular biology and cytogenetics, which are very precious for the diagnosis. The therapeutic approach consists in the complete surgical excision of the lesion that normally ensures excellent survival. Due to the potential risk of recurrence, close clinical trial is indicated. To date only 24 cases of pulmonary IMT have been described, although the prevalence is probably higher. We present a case report of a 3-year-old girl with pulmonary IMT and a brief review of known literature cases in order to highlight the most common clinical presentations, the most useful diagnostic tools and therapeutic approach.

Indexed as

anaplastic lymphoma kinase rearrangementhigh-resolution computer tomographyhistopathology assessmentinflammatory myofibroblastic tumorinflammatory pseudotumor

Identifiers

PMID29535991
PMCPMC5835069
OpenAlexW2792345384

What OpenQuestion holds

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LicenceCC BY
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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.