Angioinvasive lymphomatoid papulosis: a case report and review of the literature

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F14%3A10281108" target="_blank" >RIV/00216208:11140/14:10281108 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1097/PCR.0000000000000042" target="_blank" >http://dx.doi.org/10.1097/PCR.0000000000000042</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1097/PCR.0000000000000042" target="_blank" >10.1097/PCR.0000000000000042</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Angioinvasive lymphomatoid papulosis: a case report and review of the literature

Popis výsledku v původním jazyce

Lamphomatoid papulosis (LyP) is part of the spectrum of primary cutaneous CD30 lymphoproliferative disorders. The disease manifests with self-healing papulonodular skin lesions and exhibits a broad range of histological features. Five different histological LyP types, refered to as types A to E, have been delineated. The angioinvasive type E is characterized by angiocentric and angiodestructive tumoral infiltrates of medium sized to large CD30 atypical lymphocytes with nuclear pleomorphism. In the majority of the cases, the tumor cells express CD8, Because of its histological features and the immunophenocytpic findings, this variant of LyP is particularly prone to be misinterpreted as an aggressive lymphoma. This review addresses the clinicopathologicfeatures and differential diagnosis of LyP type E and emphasizes the role of clinicopathologic correlation in the diagnostic workup.

Název v anglickém jazyce

Angioinvasive lymphomatoid papulosis: a case report and review of the literature

Popis výsledku anglicky

Lamphomatoid papulosis (LyP) is part of the spectrum of primary cutaneous CD30 lymphoproliferative disorders. The disease manifests with self-healing papulonodular skin lesions and exhibits a broad range of histological features. Five different histological LyP types, refered to as types A to E, have been delineated. The angioinvasive type E is characterized by angiocentric and angiodestructive tumoral infiltrates of medium sized to large CD30 atypical lymphocytes with nuclear pleomorphism. In the majority of the cases, the tumor cells express CD8, Because of its histological features and the immunophenocytpic findings, this variant of LyP is particularly prone to be misinterpreted as an aggressive lymphoma. This review addresses the clinicopathologicfeatures and differential diagnosis of LyP type E and emphasizes the role of clinicopathologic correlation in the diagnostic workup.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FP - Ostatní lékařské obory

OECD FORD obor

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Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2014

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Pathology Case Reviews

ISSN

1082-9784

e-ISSN

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Svazek periodika

19

Číslo periodika v rámci svazku

4

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

4

Strana od-do

187-190

Kód UT WoS článku

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EID výsledku v databázi Scopus

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