Evidence map›Paper›PMID 27437281›Full record

ArticleJournal of clinical and diagnostic research : JCDR2016

A Case of Erythroderma Secondary to Hypereosinophilia.

Mohammed Shafi Abdulsalam, Hari Chandana Ghanta, Prabu Pandurangan, Maya Menon, Sheba S K Jacob

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical and diagnostic research : JCDR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

5 authors at 1 institution in 1 country.

Mohammed Shafi AbdulsalamPost Graduate Student, Department of Internal Medicine, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India .
Hari Chandana GhantaAssociate Consultant Physician, Department of Internal Medicine, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India .
Prabu PanduranganConsultant Haematologist, Department of Haematology, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India .
Maya MenonSenior Consultant Pathologist, Department of Pathology, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India .
Sheba S K JacobConsultant Pathologist, Department of Pathology, Greams Road, Apollo Main Hospital , Chennai, Tamil Nadu, India .
Apollo Hospitals · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypereosinophilic syndrome (HES) is a myeloproliferative disorder characterised by marked peripheral eosinophilia and end organ damage attributable to eosinophilia without secondary cause. Early recognition and treatment are essential to prevent morbidity and mortality. Cytoreduction with Steroids, Hydroxyurea and Imatinib are the main stay of treatment. Molecular studies like Fip1-like-1 fused with platelet derived growth factor receptor alpha (FIP1L1-PDGFRα) etc., are recommended in view of therapeutic implication. In this paper we report a rare case of HES developing in a lady 6 months after surgical removal of lymphangioma of spleen, which in itself is rare.

Indexed as

Adrenal insufficiencyCytoreductionLymphangioma of spleenTissue eosinophilia

Identifiers

PMID27437281
PMCPMC4948457
OpenAlexW2493382935

What OpenQuestion holds

Textmetadata
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.