Evidence map›Paper›PMID 36457206›Full record

ArticleThe American journal of case reports2022

Vanishing Lung Syndrome, or Idiopathic Giant Bullous Emphysema, with Pneumothorax, and Subcutaneous Emphysema in a 58-Year-Old Female Smoker with Chronic Obstructive Pulmonary Disease.

Haris Sohail, Yassine Kilani, Julieta Osella, Ashna Syeda Fatima Kamal, Barkha Kumari, Daniel Emnet Keftassa, Mubarak H Yusuf, Mohammad Aldiabat, Ali Horoub, Shekar Murthy

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The American journal of case reports, 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
0.8field-weighted citation impact, top 27% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

10 authors at 3 institutions in 1 country.

Haris SohailDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.ORCID 0000-0001-6720-7178
Yassine KilaniDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.
Julieta OsellaDepartment of Pulmonary and Critical Care, Spectrum Health - Michigan State University, Grand Rapids, MI, USA.
Ashna Syeda Fatima KamalDepartment of Internal Medicine, Springfield Memorial Hospital, Springfield, IL, USA.
Barkha KumariDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.
Daniel Emnet KeftassaDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.
Mubarak H YusufDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.ORCID 0000-0002-0863-8944
Mohammad AldiabatDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.
Ali HoroubDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.
Shekar MurthyDepartment of Internal Medicine, Lincoln Medical Center, Bronx, NY, USA.
Lincoln Medical Center · USMemorial Hospital · USSpectrum Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Vanishing lung syndrome (VLS), also known as idiopathic giant bullous emphysema, is a rare manifestation of chronic obstructive pulmonary disease (COPD) and usually occurs in middle-aged smokers. This report presents a 58-year-old female smoker with COPD and VLS who presented with spontaneous pneumothorax. The pneumothorax was managed with a chest tube and was later complicated by massive subcutaneous emphysema. CASE REPORT A 58-year-old woman with a past medical history of long-term smoking and COPD presented with worsening shortness of breath. Upon initial evaluation, she had tachypnea and hypoxia (SpO₂ 93%). Chest radiography revealed a new right-sided pneumothorax on top of extensive bullous disease, which the patient already had. The drainage of the pneumothorax was successful with a pigtail catheter. However, during the following night, after insertion of the pigtail catheter, the patient developed massive subcutaneous emphysema, which was confirmed with imaging. The patient remained hemodynamically stable, and diffuse subcutaneous crepitus was present on examination. The pigtail catheter was repositioned, resulting in complete resolution of the subcutaneous emphysema in the following 2 weeks. CONCLUSIONS This case highlights the importance of a timely diagnosis and management of the possible presentations and complications of VLS. Complications such as pneumothorax are life-threatening and require urgent management, taking precedence over the curative treatment for VLS, surgical bullectomy.

Indexed as

PneumothoraxPulmonary Disease, Chronic ObstructivePulmonary EmphysemaSubcutaneous EmphysemaFemaleHumansLungMiddle AgedSmokersSyndrome

Identifiers

PMID36457206
PMCPMC9724188
OpenAlexW4309756424

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.