Evidence map›Paper›PMID 25404214›Full record

ArticleJournal of cutaneous pathology2015

ALK-positive (2p23 rearranged) anaplastic large cell lymphoma with localization to the skin in a pediatric patient.

Melissa Pulitzer, Olakunle Ogunrinade, Oscar Lin, Peter Steinherz

Abstract readCase Reports
In one paragraph

Article in Journal of cutaneous pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Paediatric cutaneous lymphomas including rare subtypes: A 40-year experience at a tertiary referral centre.Journal of the European Academy of Dermatology and Venereology : JEADV · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Recent advances in cutaneous lymphoma-implications for current and future classifications.Virchows Archiv : an international journal of pathology · 2023
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Cutaneous T-cell Lymphoma.Clinics in laboratory medicine · 2017
    Review
  15. 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

4 authors at 2 institutions in 1 country.

Melissa PulitzerDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Olakunle OgunrinadeDepartment of Dermatology, Weill Cornell College of Medicine, New York, NY, USA.
Oscar LinDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Peter SteinherzDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Memorial Sloan Kettering Cancer Center · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Anaplastic large cell lymphoma (ALCL) either as primary cutaneous or nodal disease is rare in children and difficult to distinguish, which is important both prognostically and for treatment purposes. We present a case of anaplastic lymphoma kinase (ALK)+ skin-limited ALCL that highlights this challenge and draws attention to pitfalls in assessing ALK status. The patient was an 11-year old girl with a twice recurrent nodule on her right shoulder. Each biopsy revealed a deep infiltrate of atypical lymphocytes that expressed CD3, CD4, CD43, CD45RO and CD30. The initial biopsy was epithelial membrane antigen (EMA)+ with vague cytoplasmic ALK-1 positivity by immunohistochemistry, while the second biopsy was EMA+ and nuclear ALK-1+. Fluorescence in situ hybridization analysis for an ALK (2p23) rearrangement of the first specimen was negative, while an ALK gene rearrangement was present in the second specimen. Therefore, this case was treated as nodal ALCL, despite negative bone marrow and radiographic imaging studies. The patient was treated with combination chemotherapy and remains disease-free. Demonstration of nuclear ALK-positivity, ALK (2p23) gene rearrangement is suggestive of systemic ALCL. Without evidence of systemic disease, this case highlights challenges of skin-limited ALCL, whose clinical behavior as either cutaneous ALCL systemic ALCL may not be immediately apparent.

Indexed as

Anaplastic Lymphoma KinaseBiopsyChildDisease-Free SurvivalFemaleHumansLymphocytesLymphoma, Large-Cell, AnaplasticLymphoma, T-Cell, CutaneousMucin-1PrognosisReceptor Protein-Tyrosine KinasesSkin NeoplasmsTranslocation, GeneticALK protein, humanAnaplastic Lymphoma KinaseMucin-1Receptor Protein-Tyrosine Kinasesanaplastic large cell lymphomaanaplastic lymphoma kinaseEMAnodal ALCLskin-limited ALCL

Identifiers

PMID25404214
PMCPMC5108361
OpenAlexW1934945307

What OpenQuestion holds

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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.