Fadoukhair Zouhour, Lalya Issam, Amzerin Mounia, Elkhanoussi Basma, Sbitti Yassir, Boutayeb Saber, M'rabti Hind, Benjaafar Noureddine, Errihani Hassan
Department of Medical Oncology, National Institute of Oncology, Rabat, Morocco.
Pan Afr Med J. 2011;8:50. doi: 10.4314/pamj.v8i1.71168. Epub 2011 Apr 30.
Primary bone lymphoma (PBL) is a relatively uncommon entity. However, involvement of the cranial vault is an unusual manifestation of aggressive non-Hodgkin's lymphoma. We report the case of a 42-year old immunocompetent woman who presented with an enlarging mass involving the right parietal bone. Magnetic resonance imaging (MRI) of the brain revealed an expansive tumor that affects the right parietal bone. Computed tomographic (CT) scans of the abdomen, chest and pelvis were negative for lymphadenopathy or organomegaly. Biopsy of the mass showed diffuse large B-cell non-Hodgkin's lymphoma confirmed by immunohistochemical study. The patient had a complete response after 4 cycles of chemotherapy followed by external beam radiotherapy. After a follow-up of more than 9 months the patient is still in good local control without distant metastasis. The aim of our work is to report a case of Primary bone lymphoma of the cranial vault with good response to treatment combining sequential chemotherapy and radiotherapy.
原发性骨淋巴瘤(PBL)是一种相对罕见的疾病。然而,颅穹窿受累是侵袭性非霍奇金淋巴瘤的一种不寻常表现。我们报告了一例42岁免疫功能正常的女性病例,该患者出现累及右顶骨的肿块且不断增大。脑部磁共振成像(MRI)显示有一个累及右顶骨的膨胀性肿瘤。腹部、胸部和骨盆的计算机断层扫描(CT)未发现淋巴结病或器官肿大。肿块活检显示弥漫性大B细胞非霍奇金淋巴瘤,免疫组化研究得以证实。该患者在接受4个周期的化疗后接着进行外照射放疗,获得了完全缓解。经过9个多月的随访,患者局部控制良好,无远处转移。我们的工作目的是报告一例颅穹窿原发性骨淋巴瘤病例,该病例对序贯化疗和放疗联合治疗反应良好。