Evidence map›Paper›PMID 39130067›Full record

ArticleEuropean journal of case reports in internal medicine2024

A Case of Atypical Scleroderma Renal Crisis.

Ayushi Lalwani, Shefali Amin, Zohaib Yousaf, Muhammad Umer Riaz Gondal, Sami Al Ampnti, Andrew Pajak, Christopher Reggio

Abstract read
In one paragraph

Article in European journal of case reports in internal medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Ayushi LalwaniDepartment of Internal Medicine, Reading Hospital, West Reading USA.
Shefali AminDepartment of Internal Medicine, Reading Hospital, West Reading USA.
Zohaib YousafDepartment of Internal Medicine, Reading Hospital, West Reading USA.
Muhammad Umer Riaz GondalDepartment of Internal Medicine, Reading Hospital, West Reading USA.
Sami Al AmpntiDepartment of Pulmonary and Critical Care Medicine, Reading Hospital, West Reading, USA.
Andrew PajakDepartment of Pulmonary and Critical Care Medicine, Reading Hospital, West Reading, USA.
Christopher ReggioDepartment of Internal Medicine, Reading Hospital, West Reading USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present the case of a 63-year-old female diagnosed with atypical SSc in the setting of acute SRC. She was undergoing work-up for progressive dyspnoea in the outpatient setting when she was found to have newly diagnosed restrictive lung pathology and worsening renal function, thus prompting acute hospital admission. Given multisystem involvement of the pulmonary and renal systems, the differential diagnosis included autoimmune and connective tissue disorders. Although serologies were non-specific, renal biopsy confirmed scleroderma renal disease, and she was started on treatment with captopril. This case highlights the importance of clinical judgment and timely diagnosis, even when laboratory data might indicate otherwise. LEARNING POINTS: Scleroderma renal crisis (SRC) remains an important cause of morbidity and mortality in systemic sclerosis (SSc), and clinicians should have a high index of suspicion to diagnose it.The absence of specific serologic markers makes SSc diagnosis challenging and necessitates reliance on clinical findings and additional diagnostic tools such as imaging studies and tissue sampling.

Indexed as

acute hypoxic respiratory failurepericardial effusionSclerodermascleroderma renal crisis

Identifiers

PMID39130067
PMCPMC11313114

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.