Abstract
A patient with angioimmunoblastic lymphadenopathy was treated with chemotherapy to complete remission for 13 years. A single relapse, self-limited, occurred followed 2 years later by the appearance of a disseminated non-Hodgkin's lymphoma with prominent cutaneous lesions and hypogammaglobulinemia. Cells from the peripheral blood and an affected lymph node were characterized by immunologic studies as deriving from the T<inf>8</inf> subset of lymphocytes, suggesting a functional relationship between these suppressor cells and the patient's clinical manifestations.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 195-199 |
| Number of pages | 5 |
| Journal | ONCOLOGY (United States) |
| Volume | 40 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1983 |
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Keywords
- Angioimmunoblastic lymphadenopathy
- Lymphoma
- T<inf>8</inf> suppressor cells
ASJC Scopus subject areas
- Cancer Research
- Oncology
Cite this
Lymphoma of cytotoxic/suppressor T cell phenotype (T<inf>8</inf>) following angioimmunoblastic lymphadenopathy. / Rubinstein, Arye; Dauber, Leonard G.
In: ONCOLOGY (United States), Vol. 40, No. 3, 1983, p. 195-199.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Lymphoma of cytotoxic/suppressor T cell phenotype (T8) following angioimmunoblastic lymphadenopathy
AU - Rubinstein, Arye
AU - Dauber, Leonard G.
PY - 1983
Y1 - 1983
N2 - A patient with angioimmunoblastic lymphadenopathy was treated with chemotherapy to complete remission for 13 years. A single relapse, self-limited, occurred followed 2 years later by the appearance of a disseminated non-Hodgkin's lymphoma with prominent cutaneous lesions and hypogammaglobulinemia. Cells from the peripheral blood and an affected lymph node were characterized by immunologic studies as deriving from the T8 subset of lymphocytes, suggesting a functional relationship between these suppressor cells and the patient's clinical manifestations.
AB - A patient with angioimmunoblastic lymphadenopathy was treated with chemotherapy to complete remission for 13 years. A single relapse, self-limited, occurred followed 2 years later by the appearance of a disseminated non-Hodgkin's lymphoma with prominent cutaneous lesions and hypogammaglobulinemia. Cells from the peripheral blood and an affected lymph node were characterized by immunologic studies as deriving from the T8 subset of lymphocytes, suggesting a functional relationship between these suppressor cells and the patient's clinical manifestations.
KW - Angioimmunoblastic lymphadenopathy
KW - Lymphoma
KW - T<inf>8</inf> suppressor cells
UR - http://www.scopus.com/inward/record.url?scp=0020597187&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0020597187&partnerID=8YFLogxK
U2 - 10.1159/000225724
DO - 10.1159/000225724
M3 - Article
VL - 40
SP - 195
EP - 199
JO - Oncology
JF - Oncology
SN - 0890-9091
IS - 3
ER -