Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Pityriasis lichenoides chronica: stratification by molecular and phenotypic profile.

Human pathology - 1 Mar 2007

Magro Cynthia M, Crowson A Neil, Morrison Carl, Li Jingwei

Abstract excerpt

Pityriasis lichenoides (PL) has traditionally been classified as a benign papulosquamous disease. However, there is an increasing literature precedent that suggests that PL should instead be considered a form of cutaneous lymphoid dyscrasia. We prospectively encountered 46 patients with a diagnosis of PL and used immunohistochemical and multiplex polymerase chain reaction fragment size analysis to assess for...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Aged
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Phenotype

Share to Polymerase Chain Reaction

Share to T-Lymphocytes

Source

Identifiers

PMID: 17239929
DOI: 10.1016/j.humpath.2006.09.013

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pityriasis lichenoides chronica: stratification by molecular and phenotypic profile.PMID 17239929Read ↗

Pityriasis Lichenoides, Atypical Pityriasis Lichenoides, and Related Conditions: A Study of 66 Cases.Semantic proximity Read ↗

Single-cell sequencing delineates T-cell clonality and pathogenesis of the parapsoriasis disease groupSemantic proximity Read ↗

Hypopigmented mycosis fungoides: frequent expression of a CD8+ T-cell phenotype.Semantic proximity Read ↗

Mycosis fungoides: an updated review of clinicopathologic variants.Semantic proximity Read ↗

Pityriasis lichenoides: a cytotoxic T‐cell‐mediated skin disorder. Evidence of human parvovirus B19 DNA in nine casesSemantic proximity Read ↗

Lymphomatoid papulosis: A clinical and histopathologic review of 53 cases with leukocyte immunophenotyping, DNA flow cytometry, and T-cell receptor gene rearrangement studiesSemantic proximity Read ↗

Follicular mycosis fungoides: a histopathologic, immunohistochemical, and genotypic review.Semantic proximity Read ↗

Gene rearrangements and T-cell lymphomas.Semantic proximity Read ↗

Hyperpigmented mycosis fungoides: an unusual variant of cutaneous T-cell lymphoma with a frequent CD8+ phenotype.Semantic proximity Read ↗

CD8+ lymphomatoid papulosis and its differential diagnosis.Semantic proximity Read ↗

Pagetoid reticulosis (Woringer-Kolopp disease): an immunophenotypic, molecular, and clinicopathologic study.Semantic proximity Read ↗

Lymphomatoid papulosis type D: a newly described variant easily confused with cutaneous aggressive CD8-positive cytotoxic T-cell lymphoma.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.