Osanai Satoko, Oshima Shoko, Itoi Satoru, Kato Yutaka, Ryuzaki Michiko, Izuka Yuki, Tanaka Norina, Ishiyama Midori, Shinohara Akihito, Yoshinaga Kentaro, Shiseki Masayuki, Onizuka Hiromi, Nagashima Yoji, Tanaka Junji
Department of Hematology, Tokyo Women's Medical University.
Department of Surgical Pathology, Tokyo Women's Medical University.
Rinsho Ketsueki. 2023;64(2):119-124. doi: 10.11406/rinketsu.64.119.
The patient, a 56-year-old lady, also exhibited numerous lymphadenopathy, hepatosplenomegaly, hyperleukocytosis (167,200/µl, aberrant lymphocytes 91.5%), and fever. A lymph node biopsy revealed follicular lymphoma (FL), grade 1. Peripheral blood tumor cells did not express CD10, which was a distinctive characteristic of the lymph node specimen. To prevent tumor lysis syndrome (TLI), CHOP was delivered without an anti-CD20 antibody, but afterward, residual lymphoma cells were found in peripheral blood (>80%). As a result, obinutuzumab (Obi) was given on day 8 following the second round of CHOP, and the tumor cells in the peripheral blood vanished without any major side effects like TLI. She underwent six chemotherapy sessions before receiving maintenance therapy with Obi and achieving a full metabolic response. According to reports, leukemic FL exhibits negative CD10 expression in peripheral blood lymphoma cells, while leukemic mantle cell lymphoma also shows this trait. Therefore, it is important not to confuse the two types in diagnosis. Leukemic FL with significant leukocytosis is reportedly uncommon and has a bad prognosis. Our case indicates that CHOP with Obi would be a good alternative for cases like yours, however, there have been a few cases recorded. Further case accumulation or investigation is warranted.
该患者为一名56岁女性,还表现出多处淋巴结病、肝脾肿大、白细胞增多(167,200/µl,异常淋巴细胞91.5%)及发热。淋巴结活检显示为1级滤泡性淋巴瘤(FL)。外周血肿瘤细胞不表达CD10,这是淋巴结标本的一个显著特征。为预防肿瘤溶解综合征(TLS),给予CHOP方案化疗时未使用抗CD20抗体,但之后在外周血中发现残留淋巴瘤细胞(>80%)。因此,在第二轮CHOP化疗后的第8天给予奥妥珠单抗(Obi),外周血中的肿瘤细胞消失,且未出现如TLS等任何严重副作用。她接受了6个疗程的化疗,之后接受Obi维持治疗并实现完全代谢缓解。据报道,白血病性FL在外周血淋巴瘤细胞中表现为CD10表达阴性,白血病性套细胞淋巴瘤也有此特征。因此,在诊断中不要混淆这两种类型很重要。据报道,白细胞增多显著的白血病性FL并不常见且预后不良。我们的病例表明,CHOP联合Obi对类似您这样的病例可能是一个不错的选择,不过,仅有少数病例记录。有必要进一步积累病例或进行研究。