顎下リンパ節の腫脹を契機に診断に至った血管免疫芽球性T細胞リンパ腫の1例
Angioimmunoblastic T-cell lymphoma (AITL) is one of the subtypes of non-Hodgkin lymphoma. The neoplasm is characterized by aggressive, rapid growth and a poor prognosis. A standard treatment protocol has not been established. In our literature review, only one case of AITL of the head and neck was d...
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Published in | 日本口腔外科学会雑誌 Vol. 65; no. 4; pp. 257 - 262 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
社団法人 日本口腔外科学会
20.04.2019
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Online Access | Get full text |
ISSN | 0021-5163 2186-1579 |
DOI | 10.5794/jjoms.65.257 |
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Abstract | Angioimmunoblastic T-cell lymphoma (AITL) is one of the subtypes of non-Hodgkin lymphoma. The neoplasm is characterized by aggressive, rapid growth and a poor prognosis. A standard treatment protocol has not been established. In our literature review, only one case of AITL of the head and neck was diagnosed. We report a case of AITL diagnosed by submandibular lymph node biopsy. A 74-year-old woman visited our department because of a swelling in submandibular region. Magnetic resonance imaging showed multiple lymphadenopathy in the bilateral submandibular region. Positron-emission tomography-computed tomography showed the abnormal uptake of FDG in lymph nodes of the entire body. A submandibular lymph node biopsy was performed, and AITL was diagnosed histopathologically. CHOP or Hyper-CVAD, which are standard treatments for non-Hodgkin lymphoma, were proposed, but were not accepted by the patient. Alternatively, anti-CCR4 antibody therapy was conducted, but resulted in poor control of the disease. Finally, palliative care was performed until the patient died of the disease. |
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AbstractList | Angioimmunoblastic T-cell lymphoma (AITL) is one of the subtypes of non-Hodgkin lymphoma. The neoplasm is characterized by aggressive, rapid growth and a poor prognosis. A standard treatment protocol has not been established. In our literature review, only one case of AITL of the head and neck was diagnosed. We report a case of AITL diagnosed by submandibular lymph node biopsy. A 74-year-old woman visited our department because of a swelling in submandibular region. Magnetic resonance imaging showed multiple lymphadenopathy in the bilateral submandibular region. Positron-emission tomography-computed tomography showed the abnormal uptake of FDG in lymph nodes of the entire body. A submandibular lymph node biopsy was performed, and AITL was diagnosed histopathologically. CHOP or Hyper-CVAD, which are standard treatments for non-Hodgkin lymphoma, were proposed, but were not accepted by the patient. Alternatively, anti-CCR4 antibody therapy was conducted, but resulted in poor control of the disease. Finally, palliative care was performed until the patient died of the disease. |
Author | 松宮, 由香 末松, 基生 宇佐美, 悠 今井, 智章 鵜澤, 成一 竹下, 彰範 |
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References | 2) Federico M, Rudiger T, et al : Clinicopathologic characteristics of angioimmunoblastic T-cell lymphoma : analysis of the international peripheral T-cell lymphoma project. J Clin Oncol 23: 240-246, 2013. 13) Yang G, Abdelhalim F, et al : Composite Angioimmunoblastic T-Cell Lymphoma and B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Involving Both Lymph Node and Bone Marrow With Digital Gangrene. Hematopathology 3: 14-21, 2018. 14) Wang Y, Xie B, et al : Development of angioimmunoblastic T-cell lymphoma after treatment of diffuse large B-cell lymphoma: a case report and review of literature. Int J Clin Exp Pathol 7: 3432-3438, 2014. 20) Attygalle AD, Kyriakou C, et al : Histologic evolution of angioimmunoblastic T-cell lymphoma in consecutive biopsies: clinical correlation and insights into natural history and disease progression. Am J Surg Pathol 31: 1077-1088, 2007. 15) Suefuji N, Niino D, et al : Clinicopathological analysis of a composite lymphoma containing both T- and B-cell lymphomas. Pathol Int 62: 690-698, 2012. 10) 伊豆津宏二:血管免疫芽球性T細胞リンパ腫.Nippon Rinsho 72: 519-523, 2014. 17) Ishida T, Utsunomiya A, et al : Clinical significance of CCR4 expression in adult T-cell leukemia/lymphoma: its close association with skin involvement and unfavorable outcome. Clin Cancer Res 9: 3625-3634, 2003. 18) Ishida T, Inagaki H, et al : CXC chemokine receptor 3 and CC chemokine receptor 4 expression in T-cell and NK-cell lymphomas with special reference to clinicopathological significance for peripheral T-cell lymphoma, unspecified. Clin Cancer Res 10: 5494-5500, 2004. 11) 田丸淳一, 川野竜太郎, 他:悪性リンパ腫の病理.日耳鼻 112: 465-473, 2009. 3) The world health organization classification of malignant lymphomas in japan : incidence of recently recognized entities. Lymphoma Study Group of Japanese Pathologists. Pathol Int 50: 696-702, 2000. 21) Argyris PP, Koutlas IG, et al : Angioimmunoblastic T-cell lymphoma of the oral cavity presenting as gingival mass : report of the histopathologic and molecular characteristics of an unusual case featuring clonal T-cell receptor γ gene rearrangement by polymerase chain reaction. Oral Surg Oral Med Oral Pathol Oral Radiol 118: e198-204, 2014. 6) 鈴木律朗:T/NK細胞リンパ腫ガイドライン.臨血 54: 1764-1769, 2013. 16) 義江 修:ケモカイン受容体CCR4とHTLV-1感染,ATL発がん. ウイルス 58: 125-140, 2008. 1) 青笹克之, 森井英一:血管免疫芽球性T細胞リンパ腫;リンパ球増殖疾患 癌診療指針のための病理診断プラクティス.中山書店, 東京, 2010, 227-235 頁 7) (一社) 日本血液学会:末梢性T細胞リンパ腫.造血器腫瘍診療ガイドライン : 2013. Available at: http://www.jshem.or.jp/gui-hemali/2_7.html Accessed August 20, 2016. 9) 岡本昌隆:血管免疫芽球性T細胞リンパ腫−病理・病態・治療.医のあゆみ 234: 549-554, 2010. 12) Yang QX, Pei XJ, et al : Secondary cutaneous Epstein-Barr virus-associated diffuse large B-cell lymphoma in a patient with angioimmunoblastic T-cell lymphoma: a case report and review of literature. Diagn Pathol doi: 10.1186/1746-1596-7-7, 2012. Accessed July 21, 2016. 8) 平賀幸弘, 黄 純一, 他:頸部原発の血管免疫芽球性T細胞リンパ腫の1症例.日耳鼻 116: 1114-1119, 2013. 4) Niitsu N, Okamoto M, et al : Clinico-pathologic features and outcome of Japanese patients with peripheral T-cell lymphomas. Hematol Oncol 26: 152-158, 2008. 19) Ogura M, Ishida T, et al : Multicenter phase II study of mogamulizumab (KW-0761), a defucosylated anticc chemokine receptor 4 antibody, in patients with relapsed peripheral T-cell lymphoma and cutaneous T-cell lymphoma. J Clin Oncol 32: 1157-1163, 2014. 5) Dogan A, Attygalle AD, et al : Angioimmunoblastic T-cell lymphoma. Br J Haematol 121: 681-691, 2003. |
References_xml | – reference: 6) 鈴木律朗:T/NK細胞リンパ腫ガイドライン.臨血 54: 1764-1769, 2013. – reference: 21) Argyris PP, Koutlas IG, et al : Angioimmunoblastic T-cell lymphoma of the oral cavity presenting as gingival mass : report of the histopathologic and molecular characteristics of an unusual case featuring clonal T-cell receptor γ gene rearrangement by polymerase chain reaction. Oral Surg Oral Med Oral Pathol Oral Radiol 118: e198-204, 2014. – reference: 2) Federico M, Rudiger T, et al : Clinicopathologic characteristics of angioimmunoblastic T-cell lymphoma : analysis of the international peripheral T-cell lymphoma project. J Clin Oncol 23: 240-246, 2013. – reference: 8) 平賀幸弘, 黄 純一, 他:頸部原発の血管免疫芽球性T細胞リンパ腫の1症例.日耳鼻 116: 1114-1119, 2013. – reference: 12) Yang QX, Pei XJ, et al : Secondary cutaneous Epstein-Barr virus-associated diffuse large B-cell lymphoma in a patient with angioimmunoblastic T-cell lymphoma: a case report and review of literature. Diagn Pathol doi: 10.1186/1746-1596-7-7, 2012. Accessed July 21, 2016. – reference: 14) Wang Y, Xie B, et al : Development of angioimmunoblastic T-cell lymphoma after treatment of diffuse large B-cell lymphoma: a case report and review of literature. Int J Clin Exp Pathol 7: 3432-3438, 2014. – reference: 9) 岡本昌隆:血管免疫芽球性T細胞リンパ腫−病理・病態・治療.医のあゆみ 234: 549-554, 2010. – reference: 15) Suefuji N, Niino D, et al : Clinicopathological analysis of a composite lymphoma containing both T- and B-cell lymphomas. Pathol Int 62: 690-698, 2012. – reference: 3) The world health organization classification of malignant lymphomas in japan : incidence of recently recognized entities. Lymphoma Study Group of Japanese Pathologists. Pathol Int 50: 696-702, 2000. – reference: 4) Niitsu N, Okamoto M, et al : Clinico-pathologic features and outcome of Japanese patients with peripheral T-cell lymphomas. Hematol Oncol 26: 152-158, 2008. – reference: 5) Dogan A, Attygalle AD, et al : Angioimmunoblastic T-cell lymphoma. Br J Haematol 121: 681-691, 2003. – reference: 17) Ishida T, Utsunomiya A, et al : Clinical significance of CCR4 expression in adult T-cell leukemia/lymphoma: its close association with skin involvement and unfavorable outcome. Clin Cancer Res 9: 3625-3634, 2003. – reference: 19) Ogura M, Ishida T, et al : Multicenter phase II study of mogamulizumab (KW-0761), a defucosylated anticc chemokine receptor 4 antibody, in patients with relapsed peripheral T-cell lymphoma and cutaneous T-cell lymphoma. J Clin Oncol 32: 1157-1163, 2014. – reference: 11) 田丸淳一, 川野竜太郎, 他:悪性リンパ腫の病理.日耳鼻 112: 465-473, 2009. – reference: 1) 青笹克之, 森井英一:血管免疫芽球性T細胞リンパ腫;リンパ球増殖疾患 癌診療指針のための病理診断プラクティス.中山書店, 東京, 2010, 227-235 頁. – reference: 20) Attygalle AD, Kyriakou C, et al : Histologic evolution of angioimmunoblastic T-cell lymphoma in consecutive biopsies: clinical correlation and insights into natural history and disease progression. Am J Surg Pathol 31: 1077-1088, 2007. – reference: 13) Yang G, Abdelhalim F, et al : Composite Angioimmunoblastic T-Cell Lymphoma and B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Involving Both Lymph Node and Bone Marrow With Digital Gangrene. Hematopathology 3: 14-21, 2018. – reference: 7) (一社) 日本血液学会:末梢性T細胞リンパ腫.造血器腫瘍診療ガイドライン : 2013. Available at: http://www.jshem.or.jp/gui-hemali/2_7.html Accessed August 20, 2016. – reference: 10) 伊豆津宏二:血管免疫芽球性T細胞リンパ腫.Nippon Rinsho 72: 519-523, 2014. – reference: 16) 義江 修:ケモカイン受容体CCR4とHTLV-1感染,ATL発がん. ウイルス 58: 125-140, 2008. – reference: 18) Ishida T, Inagaki H, et al : CXC chemokine receptor 3 and CC chemokine receptor 4 expression in T-cell and NK-cell lymphomas with special reference to clinicopathological significance for peripheral T-cell lymphoma, unspecified. Clin Cancer Res 10: 5494-5500, 2004. |
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Title | 顎下リンパ節の腫脹を契機に診断に至った血管免疫芽球性T細胞リンパ腫の1例 |
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