Evidence map›Paper›PMID 27625787›Full record

ArticleMultidisciplinary respiratory medicine2016

Lung disease recalling paraseptal emphysema in a patient with Goltz syndrome.

Rosaria Cortese, Salvatore Savasta, Silvia Di Stasi, Tiziana Boggini, Chiara Trabatti, Roberto Dore, Giulia Maria Stella

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Multidisciplinary respiratory medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 87% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Rosaria CorteseCardiothoracic Department, Section of Pneumology, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Salvatore SavastaDepartment of Pediatrics, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Silvia Di StasiCardiothoracic Department, Section of Pneumology, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Tiziana BogginiDepartment of Pediatrics, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Chiara TrabattiDepartment of Pediatrics, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Roberto DoreUnit of Radiology, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Giulia Maria StellaCardiothoracic Department, Section of Pneumology, IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITPoliclinico San Matteo Fondazione · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGoltz syndrome is a rare, genetic disorder mainly occurring in female patients. CASE PRESENTATION: The case presented here is, to the best of our knowledge, the first description of the occurrence of lung parenchymal alterations in a young female patient affected by Goltz syndrome. Although pulmonary involvement is not known in patients affected by X-linked Goltz syndrome, the case here described is related to the even rarer autosomal form of the disease, as in this case. It is thus conceivable that in such different genetic setting the involvement of lung parenchyma may be unveiled through atypical emphysematous lesions.

conclusionThis report suggested - for the first time time - a rationale for a lung function and imaging screening in patients affected by Goltz syndrome at least in its autosomal form.

Indexed as

EmphysemaGoltz syndromeLung disease

Identifiers

PMID27625787
PMCPMC5020471
OpenAlexW2513526660

What OpenQuestion holds

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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.