Kikuchi A, Chida K, Misu T, Okita N, Takase S, Nagata T, Sakai K, Itoyama Y
Department of Neurology, Kohnan Hospital.
Rinsho Shinkeigaku. 1999 May;39(5):555-9.
We here present a case of 44-year-old woman, a carrier of human T-lymphotrophic virus type-1 (HTLV-1), who suffered from limbic encephalitis and breast cancer. In December 1997, the patient's behavior became abnormal. Three weeks later, she became markedly forgetful. At that time neurological examinations revealed that she had anterograde and retrograde amnesia, disorientation, and confabulation, although her consciousness was clear. Anti-Hu and anti-Yo antibodies and antinuclear antibodies in the serum were negative. Flow cytometric study of the peripheral blood lymphocytes showed an increased percentage of CD3+CD25+ cells, although the percentages of CD4+CD45RA+ and CD4+CD45RO+ cells were normal. Lymphocytic responses to phytohemagglutinin or concanavalin A were normal. Anti-HTLV-1 antibody was positive both in the serum and in the cerebrospinal fluid (CSF). The level of immunoglobulin G was high and two oligoclonal immunoglobulin G bands were positive in the CSF. Cytological study of the CSF showed no atypical cells. Findings for herpes simplex virus type I and II DNAs were negative with polymerase chain reaction in the CSF. There was no elevation of antibody titers against viruses including herpes simplex virus, cytomegalovirus, and measles virus, either in the serum or the CSF. Magnetic resonance imaging showed signal abnormalities in the medial portions of both temporal lobes, in particular, in the bilateral hippocampus. Six weeks after the onset, a cancerous tumor in her right breast was detected and removed by open surgery. The pathological diagnosis was invasive ductal carcinoma with neuroendocrine features. After mastectomy, anterograde and retrograde amnesia and disorientation mildly improved. The follow-up magnetic resonance imaging showed that signal abnormalities in the medial portions of both temporal lobes decreased and that the bilateral hippocampus became atrophic. We diagnosed the present case as paraneoplastic limbic encephalitis. There has been only one case report of limbic encephalitis associated with breast cancer.
我们在此报告一例44岁女性,她是1型人类嗜T淋巴细胞病毒(HTLV-1)携带者,患有边缘叶脑炎和乳腺癌。1997年12月,患者行为变得异常。三周后,她变得明显健忘。当时的神经学检查显示,尽管她意识清醒,但存在顺行性和逆行性失忆、定向障碍和虚构。血清中的抗Hu和抗Yo抗体以及抗核抗体均为阴性。外周血淋巴细胞的流式细胞术研究显示CD3+CD25+细胞百分比增加,尽管CD4+CD45RA+和CD4+CD45RO+细胞百分比正常。对植物血凝素或刀豆球蛋白A的淋巴细胞反应正常。血清和脑脊液(CSF)中的抗HTLV-1抗体均为阳性。CSF中免疫球蛋白G水平升高,两条寡克隆免疫球蛋白G带呈阳性。CSF的细胞学研究未发现非典型细胞。CSF中单纯疱疹病毒I型和II型DNA的聚合酶链反应结果为阴性。血清和CSF中针对包括单纯疱疹病毒、巨细胞病毒和麻疹病毒在内的病毒的抗体滴度均未升高。磁共振成像显示双侧颞叶内侧部分有信号异常,特别是双侧海马区。发病六周后,通过开放手术在她的右乳房发现并切除了一个癌性肿瘤。病理诊断为具有神经内分泌特征的浸润性导管癌。乳房切除术后,顺行性和逆行性失忆及定向障碍略有改善。随访磁共振成像显示双侧颞叶内侧部分的信号异常减少,双侧海马萎缩。我们将本病例诊断为副肿瘤性边缘叶脑炎。仅有一例关于与乳腺癌相关的边缘叶脑炎的病例报告。