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Statements

Subject Item
n2:RIV%2F00216208%3A11140%2F14%3A10281108%21RIV15-MSM-11140___
rdf:type
n13:Vysledek skos:Concept
dcterms:description
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 clinicopathologic features and differential diagnosis of LyP type E and emphasizes the role of clinicopathologic correlation in the diagnostic workup. 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 clinicopathologic features and differential diagnosis of LyP type E and emphasizes the role of clinicopathologic correlation in the diagnostic workup.
dcterms:title
Angioinvasive lymphomatoid papulosis: a case report and review of the literature Angioinvasive lymphomatoid papulosis: a case report and review of the literature
skos:prefLabel
Angioinvasive lymphomatoid papulosis: a case report and review of the literature Angioinvasive lymphomatoid papulosis: a case report and review of the literature
skos:notation
RIV/00216208:11140/14:10281108!RIV15-MSM-11140___
n3:aktivita
n5:I
n3:aktivity
I
n3:cisloPeriodika
4
n3:dodaniDat
n8:2015
n3:domaciTvurceVysledku
n18:5892805
n3:druhVysledku
n6:J
n3:duvernostUdaju
n12:S
n3:entitaPredkladatele
n17:predkladatel
n3:idSjednocenehoVysledku
3282
n3:idVysledku
RIV/00216208:11140/14:10281108
n3:jazykVysledku
n16:eng
n3:klicovaSlova
lymphoma; angioinvasive; CD30; lymphomatoid papulosis
n3:klicoveSlovo
n9:lymphoma n9:angioinvasive n9:CD30 n9:lymphomatoid%20papulosis
n3:kodStatuVydavatele
US - Spojené státy americké
n3:kontrolniKodProRIV
[271D9BEEEBE6]
n3:nazevZdroje
Pathology Case Reviews
n3:obor
n10:FP
n3:pocetDomacichTvurcuVysledku
1
n3:pocetTvurcuVysledku
4
n3:rokUplatneniVysledku
n8:2014
n3:svazekPeriodika
19
n3:tvurceVysledku
Kerl, Katrin Kazakov, Dmitry Kempf, Werner Hürlimann, Andreas
s:issn
1082-9784
s:numberOfPages
4
n11:doi
10.1097/PCR.0000000000000042
n14:organizacniJednotka
11140