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Article

Primary cutaneous ALCL with phosphorylated/activated cytoplasmic ALK and novel phenotype: EMA/MUC1+, cutaneous lymphocyte antigen negative.

The American journal of surgical pathology - 1 Sept 2008

Kadin Marshall E, Pinkus Jack L, Pinkus Geraldine S, Duran Ivan H, Fuller Christine E, Onciu Mihaela, Kawaguchi Hiroyuki, Morris Stephan W

Abstract excerpt

Primary cutaneous anaplastic large-cell lymphoma (ALCL) ordinarily is distinguished from systemic ALCL by clinical presentation, absence of anaplastic lymphoma kinase (ALK) expression, and immunophenotype (CLA+, EMA/MUC1-). We present an exceptional case of an elderly man with primary cutaneous ALCL and no systemic disease for a 13-year period. Recurrent skin tumors in this patient were characterized by...

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Share to Anaplastic Lymphoma Kinase
Share to Antigens, Differentiation, T-Lymphocyte

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Antigens, Neoplasm

Share to Lymphoma, Large-Cell, Anaplastic

Share to Mucin-1

Share to Neoplasm Recurrence, Local

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Source

Identifiers

PMID: 18670345
DOI: 10.1097/PAS.0b013e3181648d6d

Genes

ALK
MUC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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