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Article

Granular lymphocyte proliferative disorders: a multicenter study of 20 cases.

Annals of hematology - 1 Jun 1994

Woessner S, Feliu E, Villamor N, Zarco M A, Domingo A, Millá F, Florensa L, Rozman M, Abella E, Soler J

Abstract excerpt

A series of 20 patients with granular lymphocyte proliferative disorders (GLPD) is reported. The criterion of inclusion was presence of persistent (> or = 6 months) granular lymphocytosis in the absence of any causative illness. Diagnoses made upon analytical control in half the patients of splenomegaly (25%) and hepatomegaly (25%) were infrequent. Clinical course was nonprogressive in 17/20 patients, but two...

Topics

Aged
Aged, 80 and over
Colony-Forming Units Assay
Deltaretrovirus Antibodies
Female
Genotype
Hematopoietic Stem Cells
Humans
Immunophenotyping
Killer Cells, Natural
Lymphoproliferative Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Male

Middle Aged

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Identifiers

PMID: 7913627
DOI: 10.1007/BF01695034

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7913627-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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