De Niear Matthew A, Greer John P, Seegmiller Adam, Mawn Louise A
Medical Scientist Training Program, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Ocul Oncol Pathol. 2019 Jun;5(4):245-251. doi: 10.1159/000492832. Epub 2018 Nov 16.
Mantle cell lymphoma (MCL) is an uncommon form of non-Hodgkin lymphoma predominantly affecting male individuals of advanced age. Approximately 1-9% of cases of lymphoma affecting the orbital and ocular adnexal regions are attributed to MCL. We describe the case of a 65-year-old man with a 24-year history of MCL with initial remission followed by multiple relapses who presented with acute-onset binocular diplopia and proptosis of the left eye. Subsequent imaging demonstrated a new left superior orbital mass. Biopsy of the mass revealed two clonally related, yet distinct cellular components demonstrating the classical mantle cell morphology and large cells that appeared to have transformed to the blastoid variant of MCL. Transformation of classical MCL to the blastoid variant of MCL is rare, with few reports in the literature. The blastoid variant of MCL tends to be aggressive and associated with a poor prognosis. The case we describe represents perhaps the first report of MCL transformation observed in the orbit.
套细胞淋巴瘤(MCL)是一种罕见的非霍奇金淋巴瘤,主要影响老年男性个体。眼眶和眼附属器区域的淋巴瘤病例中,约1-9%归因于MCL。我们描述了一例65岁男性,有24年MCL病史,最初缓解后多次复发,表现为急性发作的双眼复视和左眼突出。随后的影像学检查显示左眼眶上部有一个新肿块。肿块活检显示两个克隆相关但不同的细胞成分,表现出典型的套细胞形态和似乎已转化为MCL母细胞样变异型的大细胞。经典MCL转化为MCL母细胞样变异型很罕见,文献报道很少。MCL母细胞样变异型往往具有侵袭性,预后较差。我们描述的这个病例可能是眼眶中观察到的MCL转化的首例报告。