scholarly journals A rare case of malignant triton tumor in the cerebellopontine angle

2012 ◽  
Vol 7 (1) ◽  
pp. 43 ◽  
Author(s):  
Li Gong ◽  
Xiao-Yan Liu ◽  
Wen-Dong Zhang ◽  
Xiu-Juan Han ◽  
Li Yao ◽  
...  
2017 ◽  
Vol 99 ◽  
pp. 811.e7-811.e10 ◽  
Author(s):  
Nadeem Khan ◽  
Alex Michael ◽  
Ali Choucair ◽  
Esther Bit-Ivan

2019 ◽  
Vol 2 (2) ◽  
pp. 131
Author(s):  
Venkateswarao Kommu ◽  
Rachanakehra ◽  
SudhaS Murthy ◽  
Krishnamohan Mallavarapu ◽  
Tasneem Rushdi ◽  
...  

2019 ◽  
Vol 10 (4) ◽  
pp. 73-75
Author(s):  
Sinjan Ghosh ◽  
Gautam Guha ◽  
Kaushik Roy ◽  
Annesh Bhattacharjee ◽  
Nikhil Repaka ◽  
...  

Tuberculoma involving the cerebellopontine angle is very rare. Preoperative neuroradiological features of such lesions may mimic neoplastic lesions. Our case presented with cerebellar features and multiple cranial nerve palsy. Neuroimaging mimicked CP angle neoplastic lesion. Antitubercular therapy and steroids resulted in significant clinical improvement and marked radiological reduction in size of the lesion. In our subcontinent a treatable infective cause like tuberculosis should be ruled out in CP angle lesions. Although rare but definitely a possibility to be considered.


CHEST Journal ◽  
2019 ◽  
Vol 155 (6) ◽  
pp. A334
Author(s):  
I. Chaudhry ◽  
N. Alayyaf

2000 ◽  
Vol 86 (2) ◽  
pp. 178-180 ◽  
Author(s):  
Rossana Lo Giudice ◽  
Enrico D'Ambrosio ◽  
Ferdinando Lupo ◽  
Davide Schiffer

In this case report we describe the development in the cerebellopontine angle of a very rare tumor, ceruminous adenoma. In the few cases described in the literature this tumor occurred in the external acoustic meatus. In four cases it developed in the cerebellopontine angle by infiltration of the petrous bone or by subcutaneous spread. In the present case no connection was found between the cerebellopontine angle and the external acoustic meatus. The most likely pathogenetic hypothesis in this case is that of a tumor of dysembryogenetic origin.


Neurosurgery ◽  
2009 ◽  
Vol 65 (6) ◽  
pp. E1205-E1205 ◽  
Author(s):  
Luciano Mastronardi ◽  
Raymond Taniguchi ◽  
Manuela Caroli ◽  
Francesco Crispo ◽  
Luigi Ferrante ◽  
...  

Abstract OBJECTIVE A rare case of cerebellopontine angle arachnoid cyst manifesting as hemifacial spasm (HFS) is reported. The patient is a 42-year-old woman with 10-month history of left HFS. A preoperative magnetic resonance imaging scan showed a well-demarcated area, hypointense on T1-weighted imaging and hyperintense on T2-weighted imaging, in the left cerebellopontine angle, without contrast enhancement, resembling an arachnoid cyst. METHODS The cyst was excised with microneurosurgical technique and the facial, vestibular, and acoustic nerves were completely decompressed from the arachnoid wall. RESULTS The postoperative course was uneventful, and the left HFS disappeared immediately. Histologically, the cyst wall was a typical arachnoidal membrane. Ten months after surgery, the patient is symptom free. CONCLUSION It is well-known that in approximately 10% of cases, trigeminal neuralgia can be caused by a space-occupying mass. However, the fact that HFS can also be caused by organic lesions as well as neurovascular compression is less well-known. Although the occurrence of tumor compression causing HFS has been previously recognized, cerebellopontine angle cysts have very rarely been described. The observation of a patient with a cerebellopontine angle arachnoid cyst causing HFS prompted us to review the literature relative to HFS caused by an organic lesion rather than neurovascular compression.


2016 ◽  
Vol 21 ◽  
pp. 121-124 ◽  
Author(s):  
B. Aykut ◽  
K. Wieczorek ◽  
P. Schirmacher ◽  
M.W. Büchler ◽  
K. Hoffmann

1982 ◽  
Vol 57 (6) ◽  
pp. 839-841 ◽  
Author(s):  
Virgil B. Graves ◽  
George W. Schemm

✓ The authors present a rare case of symptomatic lipoma of the cerebellopontine angle, and describe the computerized tomography and operative findings. These are tumors of maldevelopmental origin, and the three cases reported to date have shown many similarities.


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