Transcortical sensory aphasia following the unilateral left thalamic infarction— A case report

1992 ◽  
Vol 7 (3) ◽  
pp. 251-259 ◽  
Author(s):  
Shin-ichiro Maeshima ◽  
Norihiko Komai ◽  
Yasunobu Kinoshita ◽  
Masami Ueno ◽  
Ekini Nakai ◽  
...  
Nosotchu ◽  
1996 ◽  
Vol 18 (5) ◽  
pp. 415-420
Author(s):  
Keita Kawabata ◽  
Hisao Tachibana ◽  
Masanaka Takeda ◽  
Bungo Okuda ◽  
Minoru Sugita

2016 ◽  
Vol 40 (4) ◽  
pp. 751 ◽  
Author(s):  
Hye Yeon Lee ◽  
Min Jeong Kim ◽  
Bo-Ram Kim ◽  
Seong-Eun Koh ◽  
In-Sik Lee ◽  
...  

2021 ◽  
Author(s):  
Lília Tereza Diniz Nunes ◽  
Flávia S. Silva ◽  
Karyme G. Aota ◽  
Maria Beatriz Miranda. S. B. de Assis ◽  
João Fellipe B. Bento ◽  
...  

Context: The Artery of Percheron (AOP) is an uncommon anatomic vascular variation derivated from posterior cerebral artery segment P1, wich branchs to irrigate bilaterally the thalamus in it is paramedian portion. Amidst vascular cerebral events of the ischemic type, thalamic infarction occour in 11% of the cases. The typical clinical presentation is constituted by the triad: cogniyivebehavior comitente, oculomotors and consience disturbs. Case report: J.F.M.L, 51 years old, male, was found unconscious in his residence by SAMU and then interned in Stroke Room of HGP in 02/06/2020 with a lowered level of consciousness (Glasgow 8). The tests demonstrated a bilateral thalamic infarct due to Artery of Percheron Ischemia. In 02/09/2020 it evolved into a Glasgow 9 being extubated. The CT after 3 days demonstrated absence of bleeding and prophylatically initiated simvastatin, clexane, physiotherapy and phonoaudiology. In 02/15/2020, during physical exam, the pacient was lucid, presented behavior alterations, had left cervical dystonia and ataxia. The patient progressed well and was discharged the next day. Conclusions: The AOP, when occluded, results in bilateral paramedian thalamic and the rostral midbrain infarctions wich may cause diagnosis issues, mainly because of the vast specter of diferential diagnosis. In the presence of triad signals characteritic of bilateral thalamic infarction in CT, it must suspect the manifestation of such entity.


2021 ◽  
Vol 26 (4) ◽  
pp. 865-867
Author(s):  
Chien-Chung Cheng ◽  
Jia-Ying Sung ◽  
Chih-Shan Huang

Limbic encephalitis is a rare disorder mainly affecting the medial temporal lobe and is classically paraneoplastic. Autoimmune etiologies also exist, such as antibodies against leucine-rich glioma activated 1 (LGI1). Most cases of anti-LGI1 encephalitis are not associated with tumors. Subacute memory loss is the predominant feature, and most patients develop focal seizures, especially faciobrachial dystonic seizures (FBDSs). Immunotherapies usually show a good response, but are less effective in paraneoplastic cases. We report a case of steroid-responsive anti-LGI1 encephalitis with atypical presentations of sensory aphasia during relapse from rectal carcinoma, an atypical site.


Nosotchu ◽  
2013 ◽  
Vol 35 (3) ◽  
pp. 232-234
Author(s):  
Makoto Nomura ◽  
Hirotsugu Mikami ◽  
Takeshi Watanabe ◽  
Megumi Suzuki ◽  
Seiitsu Ono

BMC Neurology ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Florian Rimmele ◽  
Henning Maschke ◽  
Annette Großmann ◽  
Tim P. Jürgens

Abstract Background Numb Chin Syndrome (NCS), which is also characterized as sensory neuropathy of the mental nerve, describes a mostly unilateral numbness of the chin and lower lip. Benign and malignant diseases are known to cause this circumscribed symptom, which can easily be overlooked or misdiagnosed. In this article we present the very rare case of a clinical NCS caused by thalamic lacunar infarction. As a pure sensory stroke it is a rare variant of the Cheiro-Oral Syndrome (COS). Case presentation A 63-year-old male patient received an emergency referral to our department after the patient had noticed a feeling of numbness of the left lower lip and chin on the previous day. The neurological examination revealed an approximately 2 × 3 cm area of hypoesthesia in the area of the chin and left lower lip and the cranial MRI an acute ischemia in the right thalamus. Conclusions In this case report we introduce a patient who clinically shows an NCS. Various diseases may be responsible for NCS, including malignancies or even central neurological disorders such as multiple sclerosis. A lacunar thalamic ischemia as a cause of NCS is very rare and to our knowledge described in the literature only in the contex of a COS in three cases. We wish to remind the reader, through this case, of the purely descriptive and syndromal character of the NCS and the importance for detecting underlying diseases. Furthermore we give a brief overview of the NCS and causative disorders.


2008 ◽  
Vol 29 (6) ◽  
pp. 481-483 ◽  
Author(s):  
Thomas Jochum ◽  
Uta Kliesch ◽  
Reinhard Both ◽  
Jochen Leonhardi ◽  
Karl-Jürgen Bär

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