Hypocomplementemia and Hematological Abnormalities in Immunoblastic Lymphadenopathy and Immunoblastic Lymphadenopathy-Like T Cell Lymphoma

1996 ◽  
Vol 96 (2) ◽  
pp. 68-72 ◽  
Author(s):  
Takakazu Higuchi ◽  
Hiraku Mori ◽  
Haruo Niikura ◽  
Mitsuhiro Omine
Keyword(s):  
T Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Hematological Abnormalities ◽  
Immunoblastic Lymphadenopathy

Successful Treatment of Immunoblastic Lymphadenopathy-Like T-cell Lymphoma with Cyclosporin A

1999 ◽  
Vol 35 (3-4) ◽  
pp. 389-395 ◽  
Author(s):  
Nobuo Takemori ◽  
Junichi Kodaira ◽  
Nobuyasu Toyoshima ◽  
Teiko Sato ◽  
Hiroharu Sakurai ◽  
...  
Keyword(s):  
T Cell ◽  
Cyclosporin A ◽  
Successful Treatment ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Immunoblastic Lymphadenopathy

scholarly journals Immunoblastic lymphadenopathy-like T cell lymphoma with high level of serum Interleukin-2 and various allergic reactions.

2002 ◽  
Vol 25 (6) ◽  
pp. 452-457 ◽  
Author(s):  
Masayuki Tsujisaki ◽  
Seiya Nakahara ◽  
Yoshie Kazama ◽  
Haruo Shimizu ◽  
Mitsuru Yoshimoto ◽  
...  
Keyword(s):  
T Cell ◽  
Cell Lymphoma ◽  
Interleukin 2 ◽  
T Cell Lymphoma ◽  
Allergic Reactions ◽  
High Level ◽  
Immunoblastic Lymphadenopathy

Immunoblastic lymphadenopathy-like T-cell lymphoma complicated by multiple gastrointestinal involvement

1999 ◽  
Vol 34 (2) ◽  
pp. 253-259 ◽  
Author(s):  
Toshimichi Kaneki ◽  
Akira Kawashima ◽  
Taiji Akamatsu ◽  
Naoki Tanaka ◽  
Keishi Kubo ◽  
...  
Keyword(s):  
T Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Gastrointestinal Involvement ◽  
Immunoblastic Lymphadenopathy

Response to low-dose oral methotrexate and prednisone in two patients with angio-immunoblastic lymphadenopathy-type T-cell lymphoma

2001 ◽  
Vol 2 (6) ◽  
pp. 393-395 ◽  
Author(s):  
Gerlando Quintini ◽  
Emilio Iannitto ◽  
Vincenzo Barbera ◽  
Diamante Turri ◽  
Vito Franco ◽  
...  
Keyword(s):  
T Cell ◽  
Low Dose ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Oral Methotrexate ◽  
Dose Oral ◽  
Immunoblastic Lymphadenopathy

Immunoblastic Lymphadenopathy-Like T Cell Lymphoma Evolving into a Massive Plasma Cell Proliferation with Biclonal Paraproteinemia

1998 ◽  
Vol 100 (3) ◽  
pp. 151-155 ◽  
Author(s):  
Takakazu Higuchi ◽  
Jun-ichi Tada ◽  
Hiraku Mori ◽  
Haruo Niikura ◽  
Mitsuhiro Omine ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
T Cell ◽  
Plasma Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Immunoblastic Lymphadenopathy

scholarly journals Immunoblastic Lymphadenopathy-Like T-Cell Lymphoma Displaying Rearrangement of Both IgH and TCR.BETA. Genes after 4-Year Follow-Up of Idiopathic Eosinophilia.

1995 ◽  
Vol 34 (5) ◽  
pp. 418-423
Author(s):  
Mitsuaki TAKEDA ◽  
Kyuhei KOHDA ◽  
Yoshifumi FUJISAKI ◽  
Akiko TSUJI ◽  
Norihiro TAKAYANAGI ◽  
...  
Keyword(s):  
T Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Immunoblastic Lymphadenopathy

scholarly journals Clinicopathologic, immunophenotypic, and immunogenotypic analyses of immunoblastic lymphadenopathy-like T-cell lymphoma

Blood ◽  
1988 ◽  
Vol 72 (3) ◽  
pp. 1000-1006 ◽  
Author(s):  
K Tobinai ◽  
K Minato ◽  
T Ohtsu ◽  
K Mukai ◽  
Y Kagami ◽  
...  
Keyword(s):  
T Cell ◽  
Cell Lymphoma ◽  
T Cell Lymphoma ◽  
Chain Gene ◽  
Type I ◽  
Diffuse Type ◽  
Angioimmunoblastic Lymphadenopathy ◽  
Cell Leukemia Virus Type ◽  
Human T Cell ◽  
Immunoblastic Lymphadenopathy

Immunoblastic lymphadenopathy (IBL)-like T-cell lymphoma is a distinct peripheral T-cell lymphoma, which closely resembles angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) and/or IBL, but is characterized by focal or sheet-like proliferation of immunoblasts and pale cells of T-cell nature. In this report, 36 patients with IBL-like T-cell lymphoma were analyzed. The disease is clinically characterized by generalized lymph node swelling, hepatosplenomegaly, fever, skin rash, polyclonal hypergammaglobulinemia, marked male predominance, predilection for the elderly, and poor prognosis. There was no association with human T-cell leukemia virus type I or human immunodeficiency virus. IBL-like T-cell lymphoma may be divided into two categories (CD4+ type and CD8+ type) by surface marker analysis. It can also be divided into three categories on the basis of the histologic findings of distribution of morphologically recognizable tumor cells: nine cases of “inconspicuous type,” six cases of “patchy type,” and 21 cases of “diffuse type.” Two cases of “inconspicuous type” converted later to “diffuse type.” DNA hybridization analyses in the ten recent cases revealed that three of four “inconspicuous types” and five of six “diffuse types” showed clonal rearrangement of T-cell receptor-beta chain gene without rearrangement of immunoglobulin heavy chain gene, providing strong evidence for clonal proliferation of T cells.

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