Evidence map›Paper›PMID 30342536›Full record

ArticleDiagnostic pathology2018

An unusual case report of indolent T-cell lymphoproliferative disorder with aberrant CD20 expression involving the gastrointestinal tract and bone marrow.

Xingen Wang, Chi-Sing Ng, Cuimin Chen, Guangyin Yu, Weihua Yin

Open access · goldAbstract readCase Reports
In one paragraph

Article in Diagnostic pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. CD20Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
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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.

Xingen WangDepartment of Pathology, Shenzhen Hospital of Peking University, Lianhua road 1120, Futian district of Shenzhen, Shenzhen, 518036, China.
Chi-Sing NgDepartment of pathology, St. Teresa's Hospital, Ma Tau Wai, Hong Kong.
Cuimin ChenDepartment of Pathology, Shenzhen Hospital of Peking University, Lianhua road 1120, Futian district of Shenzhen, Shenzhen, 518036, China.
Guangyin YuDepartment of Pathology, Shenzhen Hospital of Peking University, Lianhua road 1120, Futian district of Shenzhen, Shenzhen, 518036, China.
Weihua YinDepartment of Pathology, Shenzhen Hospital of Peking University, Lianhua road 1120, Futian district of Shenzhen, Shenzhen, 518036, China. wangxg_77@163.com.
Peking University Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndolent T-cell proliferative disorder of the GIT is a rare and provisional entity in the revised WHO 2016 classification. The patients usually have prolonged survival with persistent disease even without any treatment. CASE PRESENTATION: The 46 years old male patient has been followed up for more than 6 years without chemotherapy. Repeated gastrointestinal biopsies showed expansion of the lamina propria extending to the submucosa by small to medium sized lymphocytes with minimal cytologic atypia. The lymphoid cells were positive for CD3, CD43, TIA-1, CD2, CD7 and the B-cell marker CD20; but negative for CD4, CD8, PAX5, CD56, cyclinD1, granzyme (GraB) and Epstein Barr virus-encoded RNA (EBER). Ki-67(MIB1) index was less than 10%. Molecular tests demonstrated a clonal rearrangement for T-cell receptor γ (TCR γ) gene but immunoglobulin chain (IgH, IgK, IgL) gene remained germline. Recognition of possible aberrant CD20 expression in indolent T-cell LPD is important to avoid potential diagnostic pitfall and improper treatment.

conclusionsWe present an unusual case of indolent T-cell lymphoproliferative disorder with aberrant CD20 expression, Recognition of this unusual immunophenotype of indolent T-cell LPD of GI helps to eschew misdiagnosis of B-cell and other high grade lymphomas and inappropriate aggressive treatment.

Indexed as

Cell ProliferationAntigens, CD20BiomarkersBiopsyBone Marrow DiseasesDiagnosis, DifferentialEndoscopy, GastrointestinalGastrointestinal DiseasesHumansImmunohistochemistryLymphoproliferative DisordersMaleMiddle AgedPhenotypePredictive Value of TestsPrognosisAntigens, CD20BiomarkersAberrant CD20 expressionGastrointestinal tractIndolent T-cell lymphoproliferative disorder

Identifiers

PMID30342536
PMCPMC6195681
OpenAlexW2897055832

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Registered trials

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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.