scholarly journals Pupil-sparing Isolated Fascicular Third Cranial Nerve Palsy due to Infarction: Report of a Case and Literature Review

2016 ◽  
Vol 04 (07) ◽  
Author(s):  
Min-Ju Kang ◽  
Dong-Jin Shin ◽  
Kwang-Dong Choi
2019 ◽  
pp. 112067211987327
Author(s):  
Raida Ben Salah ◽  
Sonda Kammoun ◽  
Faten Frikha ◽  
Yosra Bouattour ◽  
Imen Chabchoub ◽  
...  

Dysfunction of the third cranial nerve can be provoked by a number of different conditions. An isolated cranial neuropathy as a first clinical sign of a non-Hodgkin lymphoma is very infrequent. We represent here an atypical case of lymphoblastic lymphoma revealed by an isolated third cranial nerve palsy. The patient was managed by alternating cycles of cyclophosphamide, vincristine, and prednisone. She made a full recovery with a complete resolution of the symptomatology.


2019 ◽  
pp. 133-151 ◽  
Author(s):  
Michael S. Vaphiades ◽  
Martin W. ten Hove ◽  
Tim Matthews ◽  
Glenn H. Roberson ◽  
Alexandra Sinclair

2020 ◽  
Vol 13 (5) ◽  
pp. e234075
Author(s):  
Marco A Cárdenas-Rodríguez ◽  
Sergio A Castillo-Torres ◽  
Beatriz Chávez-Luévanos ◽  
Laura De León-Flores

The eight-and-a-half syndrome (EHS)—defined by the combination of a seventh cranial nerve palsy and an ipsilateral one-and-a-half syndrome—is a rare brainstem syndrome, which localises to the caudal tegmental region of the pons. We present a case of the EHS secondary to an inflammatory lesion on a previously healthy 26-year-old woman, with a literature review emphasising the relevance of aetiological assessment.


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