演題詳細

ポスター / Poster

ポスター 30 (Poster 30) :リンパ腫:AITL・皮膚リンパ腫

print

日程
2013年10月11日(金)
時間
16:50 - 17:50
会場
ポスター会場 / Poster (ロイトン札幌 3F ロイトンホールABCD)
座長・司会
内田 俊樹 (Toshiki Uchida):1
1:名古屋第二赤十字病院 血液・腫瘍内科
 
前へ戻る

Angioimmunoblastic T cell lymphoma complicated by endocapillary proliferative glomerulonephritis

演題番号 : PS-1-225

南野 智 (Satoru Nanno):1、中前 博久 (Hirohisa Nakamae):1、桑村 幸伸 (Yukinobu Kuwamura):2,4、石村 栄治 (Eiji Ishimura):2、坂部 真奈美 (Manami Sakabe):1、稲葉 晃子 (Akiko Inaba):1、康 史郎 (Shiro Koh):1、吉村 卓朗 (Takuro Yoshimura):1、西本 光孝 (Mitsutaka Nishimoto):1、林 良樹 (Yoshiki Hayashi):1,5、寺田 芳樹 (Yoshiki Terada):1、中根 孝彦 (Takahiko Nakane):1、康 秀男 (Hideo Koh):1、中尾 吉孝 (Yoshitaka Nakao):1、大澤 政彦 (Masahiko Ohsawa):3、日野 雅之 (Masayuki Hino):1

1:Hematology, Graduate School of Medicine, Osaka City University,Japan、2:Nephrology,Graduate School of Medicine, Osaka City University,Japan、3:Diagnostic Pathology, Graduate School of Medicine, Osaka City University,Japan、4:Department of Internal Medicine, Minami Osaka Hospital, Japan、5:Hematopoietic Stem Cell Transplantation Division, National Cancer Center Hospital,Japan

 

A 30-year-old female developed fever and multiple lymphadenopathy in September 2011.After antibiotic treatment,her symptoms improved.However,she once presented with fever and multiple lymphadenopathy again in December 2011.In addition,she suffered from nephrotic syndrome and severe edema.She was therefore admitted to our hospital to undergo a thorough examination.Renal biopsy revealed endocapillary proliferative glomerulonephritis.Since her renal function deteriorated rapidly,she was given steroid pulse therapy with methylprednisolone,followed by maintenance therapy with prednisolone.After treatment,while her renal function improved,her multiple lymphadenopathy still remained.Biopsy of the left axillary lymph node was then performed and she was diagnosed with angioimmunoblastic T-cell lymphoma(AITL).Although she received CHOP therapy,she failed to show any response.Therefore,she was given ESHAP therapy.She achieved partial response and her nephrotic syndrome also completely resolved.We have reported this case as renal dysfunction due to endocapillary proliferative glomerulonephritis complicated by AITL is extremely rare.

前へ戻る