Ulcerative colitis and acquired demyelinating neuropathy (Guillain-Barré syndrome)

1999 ◽  
Vol 54 (3) ◽  
pp. 129-130 ◽  
Author(s):  
B Roca
2019 ◽  
Vol 12 (3) ◽  
pp. 243-246 ◽  
Author(s):  
Kentaro Tominaga ◽  
Atsunori Tsuchiya ◽  
Hiroki Sato ◽  
Atsushi Kimura ◽  
Chiyumi Oda ◽  
...  

Medicine ◽  
2018 ◽  
Vol 97 (25) ◽  
pp. e11013 ◽  
Author(s):  
Zhengru Liu ◽  
Ke Zhou ◽  
Shan Tian ◽  
Weiguo Dong

2000 ◽  
Vol 122 (2) ◽  
pp. 269-270 ◽  
Author(s):  
ADI Yoskovitch ◽  
Daniel J. Enepekides ◽  
Michael P. Hier ◽  
Martin J. Black

Guillain-Barré syndrome (GBS), also known as acute idiopathic polyneuritis, is the most common acquired demyelinating neuropathy, characterized by muscular weakness and mild distal sensory loss. GBS presenting as bilateral vocal cord paralysis (BVCP) is extremely rare, with only 1 other case reported in the literature. 1 The following is a case of BVCP as the presenting symptom of GBS in an elderly man.


2021 ◽  
Vol 14 (1) ◽  
pp. e240178
Author(s):  
Mina M Raahimi ◽  
Alice Kane ◽  
Christopher EG Moore ◽  
Ahmad W Alareed

We describe a case of delayed onset, acute demyelinating neuropathy secondary to novel SARS-CoV-2 infection. A previously healthy 46-year-old man presented with bilateral leg pain and loss of sensation in his feet 53 days after having COVID-19 pneumonitis. He developed painful sensory symptoms followed by a rapidly progressive lower motor neuron weakness involving all limbs, face and respiratory muscles, needing ventilatory support. In keeping with a diagnosis of Guillain-Barré syndrome, cerebrospinal fluid examination showed albuminocytologic dissociation and nerve conduction studies supported the diagnosis of an acute inflammatory demyelinating polyradiculoneuropathy. The delayed neurological dysfunction seen in our patient following SARS-CoV-2 infection may indicate a novel mechanism of disease that is part of the emerging ‘long COVID-19 syndrome’.


2010 ◽  
Vol 16 (4) ◽  
pp. 555-556 ◽  
Author(s):  
Christoforos S. Krystallis ◽  
Dimitrios K. Kamberoglou ◽  
Grigorios B. Cheilakos ◽  
Maria N. Maltezou ◽  
Vassilios D. Tzias

2018 ◽  
Vol 6 ◽  
pp. 2050313X1877364
Author(s):  
Yong Chuan Chee ◽  
Beng Hooi Ong

Guillain-Barré Syndrome is an acquired acute autoimmune polyradiculoneuropathy that commonly presents with limb weakness and occasional cranial nerve, respiratory and autonomic involvement. Although the classic description of Guillain-Barré Syndrome is that of a demyelinating neuropathy with ascending weakness, predominant bilateral finger drop as presenting feature has rarely been reported. A characteristic pattern of weakness involving the extensor components of the fingers known as “finger drop sign” has been first described to be specific in acute motor axonal neuropathy form of Guillain-Barré Syndrome in the literature. We report a case of acute motor-sensory axonal neuropathy, which showed characteristic pattern of predominant finger extensor weakness, and provide a summary of all reported cases to date. While previous reports suggested that this is a sign that carries good prognosis, our case report suggested otherwise as the patient succumbed to respiratory and autonomic complications. Further studies are needed to evaluate the clinical significance of this peculiar sign.


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