Contralateral Trigeminal Nerve Dysfunction as a False Localizing Sign in Acoustic Neuroma: A Clinical and Electrophysiological Study

Neurosurgery ◽  
1984 ◽  
Vol 14 (3) ◽  
pp. 335-337 ◽  
Author(s):  
Koenig Matthew ◽  
Kalyan-Raman Krishna ◽  
N. Sureka Om

Abstract A 49-year-old woman presented with right facial sensory impairment due to trigeminal nerve dysfunction caused by a contralateral acoustic neuroma. The mechanism of the falsely localizing trigeminal involvement is probably displacement and distortion of the brain stem by the large mass lesion and not increased intracranial pressure. A preoperative orbicularis oculi reflex study was abnormal and indicative of right trigeminal nerve dysfunction; after surgical removal of the tumor, the orbicularis oculi reflex study was normal. We conclude that a false localizing sign of trigeminal nerve dysfunction can occur rarely on the contralateral side in patients with large posterior fossa tumors, especially tumors arising from the cerebellopontine angle, and should be considered in the differential diagnosis of hemifacial sensory disturbance.

2019 ◽  
Vol 2019 (8) ◽  
Author(s):  
Masashi Ishikawa ◽  
Hiroyuki Chou ◽  
Naoto Imamura ◽  
Yumeta Shimazu ◽  
Kazuo Ono

Abstract Malignant triton tumor (MTT) is a rare subtype of malignant peripheral nerve sheath tumors with rhabdomyoblastic differentiation. Although the condition may manifest sporadically, it typically affects adult patients with neurofibromatosis type 1. In this article, an extremely rare case of MTT with chest wall origin, which expanded into the left thoracic cavity, is reported. A 64-year-old male was admitted to the institution with sudden shortness of breath. Radiological examination revealed a large mass with massive pleural effusion occupying the patient’s left hemithorax. A percutaneous needle biopsy was performed and the patient underwent subtotal tumor resection with left pleuropneumonectomy. Immunohistochemical study of postsurgical pathologic specimens confirmed the diagnosis of MTT. Despite extensive surgical removal, tumor recurrence was reported soon after resection, leading to patient’s death 20 days after surgery due to acute respiratory failure. Investigation of rare MTT cases is necessary for understanding this condition.


SLEEP ◽  
2016 ◽  
Vol 39 (1) ◽  
pp. 19-23 ◽  
Author(s):  
Claudio Liguori ◽  
Maria Giuseppina Palmieri ◽  
Mariangela Pierantozzi ◽  
Massimo Cesareo ◽  
Andrea Romigi ◽  
...  

2020 ◽  
pp. 021849232098348
Author(s):  
Hemant Chaturvedi ◽  
Ravindra Singh Rao ◽  
Navneet Mehta ◽  
Ajeet Bana

A 63-year-old diabetic and hypertensive lady presented in New York Heart Association class III–IV dyspnea on exertion. Echocardiography showed a large mass attached to the anterior mitral leaflet and the base of the interatrial septum. After removal of the mass and excision of the anterior and posterior mitral leaflets, a bioprosthetic valve was deployed. The postoperative course was uneventful. Histopathology showed that the tumor was a high-grade rhabdomyosarcoma. Although it is a highly lethal tumor, surgical removal was indicated to relieve dyspnea, clarify the diagnosis, and improve short-term survival. Our patient survived for 8 months after surgical excision.


Sign in / Sign up

Export Citation Format

Share Document