Evidence map›Paper›PMID 33375216›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2021

Autoimmune Lymphoproliferative Syndrome in Children with Nonmalignant Organomegaly, Chronic Immune Cytopenia, and Newly Diagnosed Lymphoma

Zühre Kaya, Melek Işık, Nihan Oruklu, Serap Kirkiz, Emin Ümit Bağrıaçık, Luis M. Allende, María J. Díaz-Madroñero, Raquel Ruiz-García, Faruk Güçlü Pınarlı, Pınar Göçün Uyar and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2021. 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 84% 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

11 authors at 2 institutions in 2 countries.

Zühre KayaGazi University Faculty of Medicine, Department of Pediatric Hematology, Ankara, TurkeyORCID 0000-0002-3798-7246
Melek IşıkGazi University Faculty of Medicine, Department of Pediatric Hematology, Ankara, TurkeyORCID 0000-0002-7503-303X
Nihan OrukluGazi University Faculty of Medicine, Department of Immunology and Life Science Research Center, Ankara, TurkeyORCID 0000-0002-3241-2478
Serap KirkizGazi University Faculty of Medicine, Department of Pediatric Hematology, Ankara, TurkeyORCID 0000-0002-3885-5325
Emin Ümit BağrıaçıkGazi University Faculty of Medicine, Department of Immunology and Life Science Research Center, Ankara, TurkeyORCID 0000-0002-8066-5816
Luis M. AllendeImmunology Department and Research Institute i+12, Hospital Universitario 12 de Octubre, Madrid, SpainORCID 0000-0001-9586-8539
María J. Díaz-MadroñeroImmunology Department and Research Institute i+12, Hospital Universitario 12 de Octubre, Madrid, SpainORCID 0000-0001-8687-1517
Raquel Ruiz-GarcíaImmunology Department and Research Institute i+12, Hospital Universitario 12 de Octubre, Madrid, SpainORCID 0000-0002-8403-3613
Faruk Güçlü PınarlıGazi University Faculty of Medicine, Department of Pediatric Oncology, Ankara, TurkeyORCID 0000-0002-3241-2478
Pınar Göçün UyarGazi University Faculty of Medicine, Department of Pathology, Ankara, TurkeyORCID 0000-0003-0037-4435
Ülker KoçakGazi University Faculty of Medicine, Department of Pediatric Hematology, Ankara, TurkeyORCID 0000-0002-8701-5285
Gazi University · TRHospital Universitario 12 De Octubre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the frequency of and predictive factors for autoimmune lymphoproliferative syndrome (ALPS) in children with lymphoma, chronic immune cytopenia, and nonmalignant organomegaly. Thirty-four children with suspected ALPS (n=13, lymphoma; n=12, immune cytopenia; n=9, nonmalignant organomegaly) were included. Double-negative T-cells, lymphocyte apoptosis, and genetic findings were analyzed. Patients were stratified into two groups as proven/probable ALPS and clinically suspected patients according to the ALPS diagnostic criteria. Of the 34 patients, 18 (53%) were diagnosed with proven/probable ALPS. One patient had a mutation (c.652-2A>C) in the

Indexed as

AdolescentAnemiaAnemia, Hemolytic, AutoimmuneApoptosisAutoimmune Lymphoproliferative SyndromeChildChild, PreschoolChronic DiseaseCross-Sectional Studiesfas ReceptorFemaleHumansInfantLeukopeniaLymphadenopathyLymphomaFAS protein, humanfas ReceptorAutoimmune lymphoproliferative syndromeImmune cytopeniaLymphoma

Identifiers

PMID33375216
PMCPMC8171202
OpenAlexW3114111227

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.