Primary lymph node presentation of angiocentric lymphoma associated with features of a hemophagocytic syndrome

B. D. Kueck, C. A. Hanson, D. E. Weissman, K. Bayliss

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

The spectrum of post-thymic T-cell neoplasia includes the angiocentric immmunoproliferative lesions, a group of disorders histological exhibiting vascular infiltration and destruction; included among these disorders is angiocentric lymphoma. In contrast to the typical extranodal presentation seen in the angiocentric immunoproliferative lesions, this report describes a case of angiocentric lymphoma presenting as primary lymph node disease with clinicopathologic findings mimicking a hemophagocytic syndrome. Rearrangement of the T-cell receptor beta chain documents this case to be a clonal T-cell neoplasm. The association of this distinct histologic type of T-cell malignancy with hemophagocytic syndromes is reviewed.

Original languageEnglish (US)
Pages (from-to)104-111
Number of pages8
JournalAmerican Journal of Hematology
Volume30
Issue number2
StatePublished - 1989
Externally publishedYes

Fingerprint

Hemophagocytic Lymphohistiocytosis
Lymphoma
Lymph Nodes
T-Lymphocytes
Antigen Receptors, T-Cell, alpha-beta
Neoplasms
Blood Vessels

ASJC Scopus subject areas

  • Hematology

Cite this

Primary lymph node presentation of angiocentric lymphoma associated with features of a hemophagocytic syndrome. / Kueck, B. D.; Hanson, C. A.; Weissman, D. E.; Bayliss, K.

In: American Journal of Hematology, Vol. 30, No. 2, 1989, p. 104-111.

Research output: Contribution to journalArticle

Kueck, B. D. ; Hanson, C. A. ; Weissman, D. E. ; Bayliss, K. / Primary lymph node presentation of angiocentric lymphoma associated with features of a hemophagocytic syndrome. In: American Journal of Hematology. 1989 ; Vol. 30, No. 2. pp. 104-111.
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