Evidence map›Paper›PMID 34912138›Full record

ArticleJournal of Indian Association of Pediatric Surgeons

Congenital Pulmonary Airway Malformation - A Histomorphological Spectrum of 15 Cases: A 5-Year Study from a Tertiary Care Center.

Kanika Gupta, Vishal Singh, Shramana Mandal, Varuna Mallya, Meeta Singh, Nita Khurana, Y K Sarin

Open access · diamondAbstract read
In one paragraph

Article in Journal of Indian Association of Pediatric Surgeons. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 1 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

7 authors at 1 institution in 1 country.

Kanika GuptaDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Vishal SinghDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Shramana MandalDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Varuna MallyaDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Meeta SinghDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Nita KhuranaDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Y K SarinDepartment of Pathology and Pediatric Surgery, Maulana Azad Medical College and Associated Hospitals, New Delhi, India.
Maulana Azad Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCongenital pulmonary airway malformation (CPAM) is a rare developmental lung disease. The aim of this study is to analyze the histomorphological spectrum of CPAM in a series of 15 cases. MATERIALS AND

methodsA retrospective descriptive study of 15 cases of CPAM was carried out from 2013 to 2018 in our hospital, and cases were classified based on the Stocker's classification.

resultsThe age ranged from 4 days to 9 years (66.6% were infants). The left lung was most commonly involved (66.6%). The most common lobe was the left upper lobe (60%), followed by right lower lobe (20%). Grossly, cysts measured 0.2-5 cm, filled with mainly serous fluid with few having hemorrhagic and brownish mucoid secretions. On microscopy, single to multiple noncommunicating cysts of size 0.2-5 cm were seen, lined by ciliated columnar epithelium (60%), pseudostratified ciliated columnar epithelium (26.7%), mucin-secreting columnar epithelium (6.7%), and flattened epithelium (6.7%). Few cases showed smooth muscle (20%) and cartilage (13.3%) in the cyst wall. Chronic inflammation (73.3%) with dense histiocytic infiltrate (13.3%) was also seen. Emphysematous changes were also observed (13.3%). Cytomegalovirus inclusions (6.7%), zygomycete fungus (6.7%), and red hepatization (6.7%) were observed. The most common type was type II (60%), followed by type I (33.3%) and type IV (6.7%).

conclusionType II was the most common variant in this study. A careful observation should be done to look for fungal hyphae or viral inclusions.

Indexed as

Congenital pulmonary airway malformationcytomegalovirustype IIzygomycetes

Identifiers

PMID34912138
PMCPMC8637997
OpenAlexW3211882695

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LicenceCC BY-NC-SA
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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.