Evidence map›Paper›PMID 3323248›Full record

ArticleJournal of clinical pathology1987

Unusual immunophenotype displayed by histiocytes in haemophagocytic lymphohistiocystosis.

T Herlin, G Pallesen, T Kristensen, N Clausen

Abstract readCase Reports
In one paragraph

Article in Journal of clinical pathology, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Familial and acquired hemophagocytic lymphohistiocytosis.European journal of pediatrics · 2007
    Review
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

4 authors.

T HerlinDepartment of Pediatrics, University Institute of Pathology, Aarhus, Denmark.
G Pallesen
T Kristensen
N Clausen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive immunophenotypic studies in a 2 1/2 month old girl with haemophagocytic lymphohistiocytosis were performed to characterise the proliferating histiocytes of the disease. The cells strongly expressed conventional macrophage antigens, but unexpectedly, there was a dissociated expression of the CD1a antigen (reacting with the monoclonal antibody NA1/34 but not with OKT6) and intracellular S-100 protein by the haemophagocytic lymphohistiocytosis histiocytes. These findings indicate that there is a "hybrid" phenotype between the two main arms of the mononuclear phagocyte system--namely, Langerhans' cells and phagocytic macrophages.

Indexed as

Antibodies, MonoclonalAntigens, SurfaceFemaleHistiocytesHumansImmunoenzyme TechniquesInfantLymphatic DiseasesLymphocytosisPhagocytosisPhenotypeAntibodies, MonoclonalAntigens, Surface

Identifiers

PMID3323248
PMCPMC1141275

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.