Evidence map›Paper›PMID 18478258›Full record

ArticleVirchows Archiv : an international journal of pathology2008

Morphological variability of lymphohistiocytic variant of anaplastic large cell lymphoma (former lymphohistiocytic lymphoma according to the Kiel classification).

Wolfram Klapper, Matthias Böhm, Reiner Siebert, Karl Lennert

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Article in Virchows Archiv : an international journal of pathology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wolfram KlapperDepartment of Pathology Haematopathology Section and Lymph Node Registry, University Hospital Schleswig-Holstein, Campus Kiel, Michaelisstrasse 11, 24105 Kiel, Germany. wklapper@path.uni-kiel.de
Matthias Böhm
Reiner Siebert
Karl Lennert

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to the WHO classification, anaplastic large cell lymphoma (ALCL) is a distinct T-cell lymphoma entity with a number of morphological variants. The characteristic feature of lymphohistiocytic variant of ALCL according to the WHO classification is the abundance of histiocytes that exceed and mask the tumour cell population. In the current, study we reanalysed a historical series of 17 lymphomas, diagnosed as lymphohistiocytic lymphoma according to the criteria of the Kiel classification, with the presence of large purple macrophages (LPM) as the decisive finding for diagnosing this lymphoma subtype. We assessed the cellular composition of the tumour and correlated the results with the definition of lymphohistiocytic variant of ALCL given in the WHO classification. Although all cases in our cohort matched the criteria of ALCL according to the WHO, in 30% of the cases, the total amount of macrophages did not exceed the number of CD30-positive tumour cells. Our results indicate that the presence of LPM might be helpful to identify this subgroup of ALCL. Because the distinction of morphological subtypes of ALCL is of clinical relevance, improved criteria for subtyping ALCL are urgently needed that might include the presence LPM as one criteria.

Indexed as

AdolescentAdultAntigens, CDAntigens, CD20Antigens, Differentiation, MyelomonocyticCD3 ComplexCD68 MoleculeChildChild, PreschoolCohort StudiesFemaleHumansKi-1 AntigenLymphoma, Large-Cell, AnaplasticMacrophagesMaleAntigens, CDAntigens, CD20Antigens, Differentiation, MyelomonocyticCD3 ComplexCD68 antigen, humanCD68 MoleculeKi-1 Antigen

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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.