Tanigawa Tomohiko, Abe Ryohei, Kato Jun, Hosoe Naoki, Ogata Haruhiko, Kameyama Kaori, Okamoto Shinichiro, Mori Takehiko
Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Center for Diagnostic and Therapeutic Endoscopy, Keio University Hospital, Tokyo, Japan.
Oncotarget. 2019 May 21;10(36):3424-3429.
Duodenal-type follicular lymphoma (DFL) is a rare variant of follicular lymphoma (FL) characterized by distinctive clinical features such as localization and favorable prognosis. We herein report a case of DFL in which histological transformation into diffuse large B-cell lymphoma developed 7 years after diagnosis. The transformed lymphoma was refractory to chemotherapy, and the patient passed away due to disease progression. To date, there have been only a limited number of reported cases of histological transformation of DFL, and the clinical outcomes of those cases except our present case have been favorable, with good responses to chemotherapy. Although the histological transformation of DFL is a rare event, the clinical course of the present case suggested that it would be a fatal event and underscore the importance of the life-long management of DFL. Further accumulation of cases is required to elucidate its incidence, characteristics, and prognosis.
十二指肠型滤泡性淋巴瘤(DFL)是滤泡性淋巴瘤(FL)的一种罕见变体,其特征为具有独特的临床特征,如定位和良好的预后。我们在此报告一例DFL病例,该病例在诊断7年后发生了组织学转化为弥漫性大B细胞淋巴瘤。转化后的淋巴瘤对化疗耐药,患者因疾病进展而死亡。迄今为止,DFL组织学转化的报道病例数量有限,除我们目前的病例外,这些病例的临床结果均良好,对化疗反应良好。尽管DFL的组织学转化是一种罕见事件,但本病例的临床病程表明这可能是一个致命事件,并强调了对DFL进行终身管理的重要性。需要进一步积累病例以阐明其发病率、特征和预后。