TY - JOUR
T1 - Nodal cytotoxic lymphoma spectrum
T2 - A clinicopathologic study of 66 patients
AU - Kagami, Yoshitoyo
AU - Suzuki, Ritsuro
AU - Taji, Hirohumi
AU - Yatabe, Yasushi
AU - Takeuchi, Takahiro
AU - Maeda, Satoko
AU - Kondo, Eisei
AU - Kojima, Masaru
AU - Motoori, Tadashi
AU - Mizoguchi, Yoshikazu
AU - Okamoto, Masataka
AU - Ohnishi, Kazunori
AU - Yamabe, Hirohiko
AU - Seto, Masao
AU - Ogura, Michinori
AU - Koshikawa, Takashi
AU - Takahashi, Toshitada
AU - Kurita, Soji
AU - Morishima, Yasuo
AU - Suchi, Taizan
AU - Nakamura, Shigeo
PY - 1999/10
Y1 - 1999/10
N2 - The expression of cytotoxic granule-associated proteins has been reported in some T-cell or natural killer (NK)-cell lymphomas of mostly extranodal origin, but rarely of nodal origin except for anaplastic large cell lymphoma (ALCL) and Hodgkin's disease (HD). This study analyzed 66 nodal lymphomas expressing T-cell intracellular antigen-1 (TIA-1) and/or granzyme B to characterize the clinicopathologic spectrum of these neoplasms. Four main groups could be delineated. The first group consisted of p80/anaplastic lymphoma kinase (ALK)-positive ALCL (n = 35). The patients were 2 to 62 years of age (median age, 16 years), and the lymphomas pursued a relatively indolent clinical course. The tumors were phenotypically of either T- or null-cell type with constant expression of CD30, epithelial membrane antigen (EMA), and p80/ALK, but not CD15 or BCL2. None harbored Epstein-Bart virus (EBV). The second group consisted of peripheral T/NK-cell lymphoma, the nodal high-grade cytotoxic type (n = 13). The patients were 29 to 72 years in age (median age, 55 years), and the tumors pursued an aggressive clinical course. The tumors often showed pleomorphic, anaplastic, or centroblastoid morphology, and were featured by either EBV association or CD56 expression. The third group consisted of peripheral T-cell lymphoma, of the nodal low-grade cytotoxic type (n = 8). The patients, three men and five women, were 31 to 75 years old (median age, 61 years). Notably, six of them exhibited lymphoepithelioid (Lennert's) lymphoma. The fourth group consisted of cytotoxic Hodgkin's-like ALCL/HD (n = 10), included seven cases of Hodgkin's-like ALCL and three cases of HD, and was characterized by the presence of Reed-Sternberg cells and often the CD15+ phenotype. The patients were all men except for one woman, and they ranged in age from 24 to 84 years (median age, 62 years). The link among these four groups was reinforced by the presence of a highly characteristic large cell with horseshoelike or reniform nuclei - the frequent expression of CD30 and EMA - and the often lack of T-cell receptor-αβ. In this series, the expression of p80/ALK and CD56 was also associated with favorable and poor prognoses respectively (p < 0.001, log-rank test).
AB - The expression of cytotoxic granule-associated proteins has been reported in some T-cell or natural killer (NK)-cell lymphomas of mostly extranodal origin, but rarely of nodal origin except for anaplastic large cell lymphoma (ALCL) and Hodgkin's disease (HD). This study analyzed 66 nodal lymphomas expressing T-cell intracellular antigen-1 (TIA-1) and/or granzyme B to characterize the clinicopathologic spectrum of these neoplasms. Four main groups could be delineated. The first group consisted of p80/anaplastic lymphoma kinase (ALK)-positive ALCL (n = 35). The patients were 2 to 62 years of age (median age, 16 years), and the lymphomas pursued a relatively indolent clinical course. The tumors were phenotypically of either T- or null-cell type with constant expression of CD30, epithelial membrane antigen (EMA), and p80/ALK, but not CD15 or BCL2. None harbored Epstein-Bart virus (EBV). The second group consisted of peripheral T/NK-cell lymphoma, the nodal high-grade cytotoxic type (n = 13). The patients were 29 to 72 years in age (median age, 55 years), and the tumors pursued an aggressive clinical course. The tumors often showed pleomorphic, anaplastic, or centroblastoid morphology, and were featured by either EBV association or CD56 expression. The third group consisted of peripheral T-cell lymphoma, of the nodal low-grade cytotoxic type (n = 8). The patients, three men and five women, were 31 to 75 years old (median age, 61 years). Notably, six of them exhibited lymphoepithelioid (Lennert's) lymphoma. The fourth group consisted of cytotoxic Hodgkin's-like ALCL/HD (n = 10), included seven cases of Hodgkin's-like ALCL and three cases of HD, and was characterized by the presence of Reed-Sternberg cells and often the CD15+ phenotype. The patients were all men except for one woman, and they ranged in age from 24 to 84 years (median age, 62 years). The link among these four groups was reinforced by the presence of a highly characteristic large cell with horseshoelike or reniform nuclei - the frequent expression of CD30 and EMA - and the often lack of T-cell receptor-αβ. In this series, the expression of p80/ALK and CD56 was also associated with favorable and poor prognoses respectively (p < 0.001, log-rank test).
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U2 - 10.1097/00000478-199910000-00003
DO - 10.1097/00000478-199910000-00003
M3 - Article
C2 - 10524519
AN - SCOPUS:0032845234
SN - 0147-5185
VL - 23
SP - 1184
EP - 1200
JO - American Journal of Surgical Pathology
JF - American Journal of Surgical Pathology
IS - 10
ER -