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

Splenic lymphoid subsets with less well-recognized phenotypes mimic aberrant antigen expression.

American journal of clinical pathology - 1 Dec 2013

Aggarwal Nidhi, Fischer Jason, Swerdlow Steven H, Craig Fiona E

Abstract excerpt

OBJECTIVES: Flow cytometry can assist in the diagnosis of lymphoma by identifying aberrant antigen expression. Recognition of aberrancy requires knowledge of the phenotype of normal lymphoid cells. METHODS: Lymphoid subsets were characterized in 20 spleens removed for traumatic rupture, using 8-color flow cytometry. RESULTS: Normal variation in splenic lymphoid subsets was highlighted and several well-recognized...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Antigens, CD
Share to B-Lymphocyte Subsets

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

Share to Flow Cytometry

Share to Immunophenotyping

Share to Lymphoma

Share to Spleen

Share to T-Lymphocyte Subsets

Source

Identifiers

PMID: 24225744
DOI: 10.1309/AJCPPIBH3I1VRWXQ

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

Splenic lymphoid subsets with less well-recognized phenotypes mimic aberrant antigen expression.PMID 24225744Read ↗

Closing the gap between biology and classification in splenic B‐cell lymphomasSemantic proximity Read ↗

Splenic marginal zone lymphoma: from genetics to management.Semantic proximity Read ↗

Diagnosis of splenic B-cell lymphomas in the bone marrow: a review of histopathologic, immunophenotypic, and genetic findings.Semantic proximity Read ↗

A Single-center Experience in Splenic Diffuse Red Pulp Lymphoma Diagnosis.Semantic proximity Read ↗

Splenic diffuse red pulp small-B cell lymphoma: toward the emergence of a new lymphoma entity.Semantic proximity Read ↗

Classification of lymphoid neoplasms: the microscope as a tool for disease discoverySemantic proximity Read ↗

NOTCH1, TP53, and MAP2K1 Mutations in Splenic Diffuse Red Pulp Small B-cell Lymphoma Are Associated With Progressive Disease.Semantic proximity Read ↗

Splenic red pulp lymphoma with numerous basophilic villous lymphocytes: a distinct clinicopathologic and molecular entity?Semantic proximity Read ↗

Immunoarchitectural patterns in splenic marginal zone lymphoma: correlations with chromosomal aberrations, IGHV mutations, and survival. A study of 76 cases.Semantic proximity Read ↗

Splenic marginal zone lymphoma.Semantic proximity Read ↗

Comparative phenotypes of peripheral blood and spleen cells from cancer patients.Semantic proximity Read ↗

Splenic marginal zone lymphoma: current knowledge and future directions.Semantic proximity Read ↗

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