Bonametti A M, Baldy J L, Bortoliero A L, de Maio C M, Passos J do N, Takata P K, de Pauli D S, Guimarães J C, Anzai E T, Elisbão M do C
Departamento de Clínica Médica, Universidade Estadual de Londrina, Paraná, Brasil.
Rev Inst Med Trop Sao Paulo. 1994 Jan-Feb;36(1):27-32.
Twenty seven cases of neurocysticercosis, with clinical picture of acute meningitis, are described. Twenty (74.1%) patients are male; the age was 4 to 42 years (23.6 +/- 11.7 years). The etiologic diagnosis was defined by the complement fixation test (Weinberg) and/or enzyme-linked immunosorbent assay (ELISA) for cysticercosis in the cerebrospinal fluid (c. s. f.). Six patients that realized cranial computerized tomographic scan resembling neurocysticercosis. Twenty one (77.8%) have predominance of lymphomononuclear cells in the c. s. f. obtained in the admission to the hospital; in 6 (22.2%) there were predominance of polymorphonuclear neutrophils. In this c. s. f. lymphomononuclear pleocytosis and in three that have c. s. f. neutrophil pleocytosis, suggesting the diagnosis of neurocysticercosis. The treatment of acute neurocysticercosis was made with dexamethasone. All the patients survived and were transferred to the ambulatory of Neurology for follow-up and complementary treatment.
本文描述了27例表现为急性脑膜炎临床症状的神经囊尾蚴病病例。其中20例(74.1%)为男性;年龄在4至42岁之间(平均23.6±11.7岁)。通过脑脊液囊尾蚴病补体结合试验(温伯格法)和/或酶联免疫吸附测定(ELISA)明确病因诊断。6例患者头颅计算机断层扫描结果疑似神经囊尾蚴病。21例(77.8%)患者入院时脑脊液中以淋巴细胞和单核细胞为主;6例(22.2%)以多形核中性粒细胞为主。在这些脑脊液呈淋巴细胞增多的病例以及3例脑脊液呈中性粒细胞增多的病例中,均提示神经囊尾蚴病的诊断。急性神经囊尾蚴病采用地塞米松进行治疗。所有患者均存活,并被转至神经科门诊进行随访及辅助治疗。