amyotrophic lateral sclerosis in a patient with behçet’s ‎disease

نویسندگان

a. borhani haghighi departments of neurology and nemazee hospital, shiraz university of medical sciences, shiraz, iran.

n. ashjazadeh departments of neurology and nemazee hospital, shiraz university of medical sciences, shiraz, iran.

a.r. nikseresht departments of neurology and nemazee hospital, shiraz university of medical sciences, shiraz, iran.

s. samangooei departments internal medicine, nemazee hospital, shiraz university of medical sciences, shiraz, iran.

چکیده

behçet’s ‎ disease is a multisystem vasculitis. its neurological involvement mostly includes parenchymal and non-parenchymal central nervous system manifestations. peripheral nervous system presentations are rare. a 32-yr-old male patient who fulfilled the international study group criteria for behçet’s disease, referred to our center with walking difficulty and repeated falling downs. neurological examination revealed weakness, wasting and fasciculation of distal muscles associated with corticospinal signs. neuroimaging data were insignificant but electrodiagnostic studies were in favor of motor neuron disease. to best of our knowledge, this is the first report of association of amyotrophic lateral sclerosis (als) and behçet’s disease.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Amyotrophic Lateral Sclerosis in a Patient with Behçet’s ‎Disease

Behçet’s ‎disease is a multisystem vasculitis. Its neurological involvement mostly includes parenchymal and non-parenchymal central nervous system manifestations. Peripheral nervous system presentations are rare. A 32-yr-old male patient who fulfilled the international study group criteria for Behçet’s disease, referred to our center with walking difficulty and repeated falling downs. Neurologi...

متن کامل

Thoracic Syringomyelia in a Patient with Amyotrophic Lateral Sclerosis

We report a patient with bulbar-onset, clinically defined, sporadic amyotrophic lateral sclerosis bearing an isolated syringomyelia of the lower thoracic portion of the spinal cord. This is a very unusual association between two rare and progressive disorders, both affecting the spinal motoneurons. Syringomyelia might have acted as a phenotypic modifier in this ALS patient.

متن کامل

Amyotrophic lateral sclerosis in a patient with leprosy peripheral neuropathy.

Peripheral neuropathy leading to sequelae is the most important complication of leprosy. The radial, ulnar, median, common peroneal, and posterior tibial nerves are the most commonly involved peripheral nerves in leprosy. Clinical manifestations of such involvement include anaesthesia, paraesthesia, and paralysis, and commonly found disabilities are clawing of the fingers and weakness of pinch,...

متن کامل

Use of Sugammadex in a Patient with Amyotrophic Lateral Sclerosis

OBJECTIVE To report on general anesthesia management in amyotrophic lateral sclerosis. CASE PRESENTATION AND INTERVENTION A 47-year-old man presented with fracture of the humerus. The patient was diagnosed with amyotrophic lateral sclerosis. General anesthesia was induced with propofol, rocuronium and remifentanil. After uneventful surgical repair, TOF (train-of-four) ratio reached >0.90 at t...

متن کامل

Pincer Nail Deformity in a Patient with Amyotrophic Lateral Sclerosis

Although several manifestations of skin involvement in cases of amyotrophic lateral sclerosis (ALS) have been reported, the pincer nail deformity has not been previously reported in a patient with ALS. The pincer nail deformity is characterized by distortion of the shape of the nail with transverse over curvature and may be associated with systemic diseases and certain medications. We herein de...

متن کامل

Evaluation of Pulmonary Function Test in Patients with Amyotrophic lateral sclerosis and its correlation with the symptoms of the disease

Introduction: Amyotrophic lateral sclerosis (ALS) is a neurogenic progressive disease that leads to muscle atrophy. The purpose of this study was to evaluate pulmonary function test (PFT) in patients with ALS and its correlation with ASL symptoms. Materials and Methods: This cross-sectional study was performed on 32 ALS patients at Ghaem Hospital, Mashhad...

متن کامل

منابع من

با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید


عنوان ژورنال:
iranian journal of medical sciences

جلد ۳۰، شماره ۴، صفحات ۱۹۴-۰

کلمات کلیدی

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023