scholarly journals Pure trigeminal motor neuropathy with an antecedent infection: a case report

2014 ◽  
Vol 54 (6) ◽  
pp. 515-517 ◽  
Author(s):  
Jun Tsugawa ◽  
Shinji Ouma ◽  
Jiro Fukae ◽  
Yoshio Tsuboi ◽  
Yoshimitsu Maki ◽  
...  
2010 ◽  
Vol 50 (8) ◽  
pp. 561-565
Author(s):  
Yoshiko Murata ◽  
Tomoko Okamoto ◽  
Yoshiyuki Kondo ◽  
Norio Chihara ◽  
Yoshihiko Furusawa ◽  
...  

2019 ◽  
Vol 18 (4) ◽  
pp. 529 ◽  
Author(s):  
Seyed M. M. Mirzaei ◽  
Ayob Akbari ◽  
Omid Mehrpour ◽  
Nasim Zamani

Opium users may present with central or peripheral nervous system-related symptoms, gastrointestinal complications and anaemia; in such cases, lead poisoning should be suspected and chelation therapy initiated as soon as possible. We report a 64-year-old male patient with a 20-year history of opium addiction who was referred to the Imam Reza Hospital, Birjand, Iran, in 2017 with severe motor neuropathy and paresis in both upper limbs. His primary symptoms were generalised weakness, abdominal and bone pain, constipation and lower limb paraesthesia that had started several months prior. In addition, he reported severe progressive bilateral paresis of the upper limbs of one month’s duration. A diagnosis of lead poisoning was confirmed by a blood lead level of 140 μg/dL. The patient underwent chelation therapy after which he improved significantly. At a one-year follow-up visit, he was neurologically intact and symptom-free.Keywords: Opium Dependence; Lead Poisoning; Lead-Induced Nervous System Diseases; Paresthesia; Case Report; Iran.


PM&R ◽  
2011 ◽  
Vol 3 ◽  
pp. S202-S202
Author(s):  
George C. Christolias ◽  
Francis Lopez ◽  
John G. Sollenberger

2000 ◽  
Vol 81 (7) ◽  
pp. 995-998 ◽  
Author(s):  
Yoon-Kyoo Kang ◽  
Eun-Ha Lee ◽  
Miriam Hwang
Keyword(s):  

2016 ◽  
Vol 62 ◽  
pp. 51-57 ◽  
Author(s):  
Hidetoshi Ishigaki ◽  
Takuya Hiraide ◽  
Yoshifumi Miyagi ◽  
Taiju Hayashi ◽  
Tomoko Matsubayashi ◽  
...  

2020 ◽  
Vol 11 ◽  
pp. 230
Author(s):  
Brandon Emilio Bertot ◽  
Melissa Lo Presti ◽  
Katie Stormes ◽  
Jeffrey S. Raskin ◽  
Andrew Jea ◽  
...  

Background: Trigeminal schwannomas are rare tumors of the trigeminal nerve. Depending on the location, from which they arise along the trigeminal nerve, these tumors can present with a variety of symptoms that include, but are not limited to, changes in facial sensation, weakness of the masticatory muscles, and facial pain. Case Description: We present a case of a 16-year-old boy with an atypical presentation of a large trigeminal schwannoma: painless malocclusion and unilateral masticatory weakness. This case is the first documented instance; to the best of our knowledge, in which a trigeminal schwannoma has led to underbite malocclusion; it is the 19th documented case of unilateral trigeminal motor neuropathy of any etiology. We discuss this case as a unique presentation of this pathology, and the relevant anatomy implicated in clinical examination aid in further understanding trigeminal nerve pathology. Conclusion: We believe our patient’s underbite malocclusion occurred secondary to his trigeminal schwannoma, resulting in associated atrophy and weakness of the muscles innervated by the mandibular branch of the trigeminal nerve. Furthermore, understanding the trigeminal nerve anatomy is crucial in localizing lesions of the trigeminal nerve.


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