Tasca Giorgio, Iorio Raffaele, Basile Umberto, Lauriola Libero, Tartaglione Raffaele, Mirabella Massimiliano, Ricci Enzo, Sabatelli Mario
Institute of Neurology, Catholic University School of Medicine, Rome, Italy.
J Neurol Sci. 2009 Sep 15;284(1-2):203-4. doi: 10.1016/j.jns.2009.04.035. Epub 2009 May 9.
We report an association between histologically confirmed progressive multifocal leukoencephalopathy (PML) and an extremely rare humoral immunodeficiency disease, Franklin disease. In our patient, clinical presentation has been typical and prompted us, together with radiological findings, to perform a brain biopsy to confirm the diagnosis even if there was no evidence of any other risk factor except hypogammaglobulinemia. We suggest that PML should be suspected in patients in whom immunosuppression is not obvious (i.e. not only in the setting of HIV infection or disseminated end-stage lymphomas) and involves defects in humoral immunity.
我们报告了组织学确诊的进行性多灶性白质脑病(PML)与一种极为罕见的体液免疫缺陷疾病——富兰克林病之间的关联。在我们的患者中,临床表现具有典型性,即便除低丙种球蛋白血症外没有任何其他危险因素的证据,其临床表现及影像学检查结果仍促使我们进行脑活检以确诊。我们建议,对于免疫抑制不明显(即不仅限于HIV感染或播散性终末期淋巴瘤的情况)且存在体液免疫缺陷的患者,应怀疑患有PML。