Evidence map›Paper›PMID 35910054›Full record

ArticleThe Pan African medical journal2022

[Erdheim-Chester disease: an aggressive systemic disease treated with cladribine with favorable outcome (a case report)].

Najat Lasri, Fatimaezzahra Lahlimi, Mohammed Ilias Tazi

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

Article in The Pan African medical journal, 2022. 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
0.2field-weighted citation impact, top 47% 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, 2 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

3 authors at 1 institution in 1 country.

Najat LasriService d'Hématologie Clinique et de Greffe de Moelle, Centre Hospitalier Universitaire Mohammed VI, Faculté de Médecine et de Pharmacie, Université Cadi Ayyad, Marrakech, Maroc.
Fatimaezzahra LahlimiService d'Hématologie Clinique et de Greffe de Moelle, Centre Hospitalier Universitaire Mohammed VI, Faculté de Médecine et de Pharmacie, Université Cadi Ayyad, Marrakech, Maroc.
Mohammed Ilias TaziService d'Hématologie Clinique et de Greffe de Moelle, Centre Hospitalier Universitaire Mohammed VI, Faculté de Médecine et de Pharmacie, Université Cadi Ayyad, Marrakech, Maroc.
Cadi Ayyad University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erdheim-Chester disease (ECD) is a form of non-langerhans histiocytosis mainly affecting men, whose pathophysiology is poorly understood. Clinical picture is heterogeneous. The presence of hair kidney sign on Ct scan is pathognomonic. Diagnosis is based on anatomopathological examination. We here report the case of a 50-year old patient presenting with disorders of equilibrium and slow speech as well as general health deterioration Clinical examination showed cerebellar ataxia. Radiological and pathological investigations showed aggressive systemic ECD. cladribine-based treatment was initiated with satisfactory outcome. ECD is an extremely rare disease. Systemic forms are generally associated with poor prognosis and are refractory to treatment, unlike in the case of our patient who was treated with cladribine with good outcome.

Indexed as

Cerebellar AtaxiaErdheim-Chester DiseaseCladribineHumansMaleMiddle AgedRadiographyTomography, X-Ray ComputedCladribinecase reportcladribineErdheim-Chester diseaseNon-langerhanian histiocytosissystemic disease

Identifiers

PMID35910054
PMCPMC9288114
OpenAlexW4289457315

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.