Alcalá H
Departamento de Neurología, Hospital Infantil de México Federico Gómez, D.F.
Bol Med Hosp Infant Mex. 1993 Feb;50(2):136-44.
Between June 1988 to January 1991 a total of 246 children with acute flaccid paralysis (AFP) were seen at Hospital Infantil de México, Federico Gómez which was the center of study for AFP for the Poliomyelitis Eradication Program of Mexico. Of the 246 children, 42 has poliomyelitis (17%); 156 has Guillain-Barré syndrome (GBS) (63.4%); 16 had traumatic neuritis of the sciatic nerve secondary to IM injections (TNC) (6.5%); five had transverse myelitis (2%); the rest (27) had other diseases misdiagnosed as polio (10.9%). The basic clinical characteristics for the diagnosis of poliomyelitis are: myalgias and fever at the onset AFP, paralysis is asymmetrical, of distal predominance and causes severe muscular atrophy and skeletal deformities; the GBS presents as an ascending, symmetrical, areflexic paralysis of distal predominance. It does not causes atrophy or deformities. TNC presents several days after IM injections with pain and hypothermia in the affected limbs; TM is a flaccid, symmetrical paraparesis with neurogenic bladder and a sensory level. CSF and neurophysiological studies (EMG and NCV) are very useful for diagnosis. Other entities misdiagnosed as poliomyelitis were: osteoarticular trauma, myopathies and dystrophies, viral myositis, acute cerebellitis, retroperitoneal tumors and upper motor neuron syndromes. Viral studies in stool specimens are essential for the diagnosis of poliomyelitis.
1988年6月至1991年1月期间,墨西哥费德里科·戈麦斯儿童医院共收治了246例急性弛缓性麻痹(AFP)患儿,该院是墨西哥脊髓灰质炎根除计划中AFP的研究中心。在这246例患儿中,42例患有脊髓灰质炎(17%);156例患有吉兰 - 巴雷综合征(GBS)(63.4%);16例因肌肉注射继发坐骨神经创伤性神经炎(TNC)(6.5%);5例患有横贯性脊髓炎(2%);其余27例(10.9%)患有被误诊为脊髓灰质炎的其他疾病。脊髓灰质炎诊断的基本临床特征为:AFP起病时伴有肌痛和发热,麻痹不对称,以远端为主,可导致严重肌肉萎缩和骨骼畸形;GBS表现为进行性、对称性、无反射性麻痹,以远端为主,不引起萎缩或畸形。TNC在肌肉注射后数天出现,受累肢体疼痛和体温过低;TM是一种伴有神经源性膀胱和感觉平面的弛缓性、对称性截瘫。脑脊液和神经生理学研究(肌电图和神经传导速度)对诊断非常有用。其他被误诊为脊髓灰质炎的疾病有:骨关节创伤、肌病和营养不良、病毒性肌炎、急性小脑炎、腹膜后肿瘤和上运动神经元综合征。粪便标本的病毒学研究对脊髓灰质炎的诊断至关重要。