Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases

Based on histologic and genetic patterns, the current World Health Organization (WHO) classification distinguishes six subtypes of lymphomatoid papulosis (Lyp). The aim of our article was to analyze the frequency of histologic and immunohistochemical features of different Lyp subtypes reported in th...

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Main Authors: Torben Fricke, Werner Kempf, Michael P. Schön, Christina Mitteldorf
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Dermatopathology
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Online Access:https://www.mdpi.com/2296-3529/12/1/6
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author Torben Fricke
Werner Kempf
Michael P. Schön
Christina Mitteldorf
author_facet Torben Fricke
Werner Kempf
Michael P. Schön
Christina Mitteldorf
author_sort Torben Fricke
collection DOAJ
description Based on histologic and genetic patterns, the current World Health Organization (WHO) classification distinguishes six subtypes of lymphomatoid papulosis (Lyp). The aim of our article was to analyze the frequency of histologic and immunohistochemical features of different Lyp subtypes reported in the literature. We used PubMed advanced search builder to systematically review and evaluate English and German literature of Lyp from 1968 to April 2022. We considered only papers in which histopathologic features were mentioned in detail. We identified 48 publications with a total of 518 cases. The diagnoses were based on the diagnostic criteria at the time of publication. In Lyp A and Lyp B a CD8+ phenotype was more often reported than expected (53% and 52%, respectively). A double positive phenotype (CD4+/CD8+) was found in 28% of Lyp E and a double negative (CD4-/CD8-) in 50% of Lyp with 6p25.3 rearrangement. High rates of folliculo- and syringotropism were reported in both Lyp A and B. Surprisingly, strong epidermotropism occurred in 20/38 (53%) cases reported as Lyp B and in 43/64 (67%) of Lyp D cases. The predominating phenotype in Lyp D was CD8+, while TIA-1/granzymeB/perforin expression was reported in 37/46 (80%), and CD56 was expressed in 13/47 (28%) of the investigated cases. The limitation of the data is due to the retrospective approach with diagnostic criteria changing over time and on a case selection in some publications. However, the data indicate that the Lyp subtypes overlap more than assumed. They also show that a prospective study is needed to obtain valid data on the frequency distribution of certain histopathologic criteria.
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spelling doaj-art-280a8eb1537f4f6a8b2795a4ab9bbff82025-08-20T02:42:40ZengMDPI AGDermatopathology2296-35292025-02-01121610.3390/dermatopathology12010006Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published CasesTorben Fricke0Werner Kempf1Michael P. Schön2Christina Mitteldorf3Department of Dermatology, Venereology and Allergology, University Medical Center Göttingen, 37075 Göttingen, GermanyKempf und Pfaltz Histologische Diagnostik, 8050 Zürich, SwitzerlandDepartment of Dermatology, Venereology and Allergology, University Medical Center Göttingen, 37075 Göttingen, GermanyDepartment of Dermatology, Venereology and Allergology, University Medical Center Göttingen, 37075 Göttingen, GermanyBased on histologic and genetic patterns, the current World Health Organization (WHO) classification distinguishes six subtypes of lymphomatoid papulosis (Lyp). The aim of our article was to analyze the frequency of histologic and immunohistochemical features of different Lyp subtypes reported in the literature. We used PubMed advanced search builder to systematically review and evaluate English and German literature of Lyp from 1968 to April 2022. We considered only papers in which histopathologic features were mentioned in detail. We identified 48 publications with a total of 518 cases. The diagnoses were based on the diagnostic criteria at the time of publication. In Lyp A and Lyp B a CD8+ phenotype was more often reported than expected (53% and 52%, respectively). A double positive phenotype (CD4+/CD8+) was found in 28% of Lyp E and a double negative (CD4-/CD8-) in 50% of Lyp with 6p25.3 rearrangement. High rates of folliculo- and syringotropism were reported in both Lyp A and B. Surprisingly, strong epidermotropism occurred in 20/38 (53%) cases reported as Lyp B and in 43/64 (67%) of Lyp D cases. The predominating phenotype in Lyp D was CD8+, while TIA-1/granzymeB/perforin expression was reported in 37/46 (80%), and CD56 was expressed in 13/47 (28%) of the investigated cases. The limitation of the data is due to the retrospective approach with diagnostic criteria changing over time and on a case selection in some publications. However, the data indicate that the Lyp subtypes overlap more than assumed. They also show that a prospective study is needed to obtain valid data on the frequency distribution of certain histopathologic criteria.https://www.mdpi.com/2296-3529/12/1/6lymphomatoid papulosisCD30+ lymphoproliferative disorderssubtypeshistopathologyimmunohistochemistry
spellingShingle Torben Fricke
Werner Kempf
Michael P. Schön
Christina Mitteldorf
Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases
Dermatopathology
lymphomatoid papulosis
CD30+ lymphoproliferative disorders
subtypes
histopathology
immunohistochemistry
title Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases
title_full Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases
title_fullStr Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases
title_full_unstemmed Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases
title_short Histologic and Immunohistochemical Patterns in Lymphomatoid Papulosis: A Systematic Review of Published Cases
title_sort histologic and immunohistochemical patterns in lymphomatoid papulosis a systematic review of published cases
topic lymphomatoid papulosis
CD30+ lymphoproliferative disorders
subtypes
histopathology
immunohistochemistry
url https://www.mdpi.com/2296-3529/12/1/6
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AT wernerkempf histologicandimmunohistochemicalpatternsinlymphomatoidpapulosisasystematicreviewofpublishedcases
AT michaelpschon histologicandimmunohistochemicalpatternsinlymphomatoidpapulosisasystematicreviewofpublishedcases
AT christinamitteldorf histologicandimmunohistochemicalpatternsinlymphomatoidpapulosisasystematicreviewofpublishedcases