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Hemorrhagic schwannoma of the trochlear nerve: Case report and a review of the literature.


ABSTRACT:

Background

Schwannomas of the trochlear nerve with the absence of systemic neurofibromatosis are considerably uncommon, especially complicated by intra-tumoral hemorrhage. Due to the lack of typical clinical manifestations and imaging findings, a definite diagnosis of trochlear schwannomas before surgery is particularly difficult.

Case presentation

We report the case of a 64-year-old female patient who presented with a unilaterally intermittent headache of 2-month duration and without a remarkable neurological deficit at admission. Imaging studies revealed a well-demarcated cystic-solid lesion with mixed signals beside the brainstem and suprasellar cisterna. The patient underwent a surgical operation with total resection of the tumor by a subtemporal surgical approach. The tumor was intraoperatively found to originate from the trochlear nerve and was pathologically confirmed as a hemorrhagic schwannoma with cystic degeneration.

Conclusions

We describe this case in detail and conduct a concomitant survey of the literature, summarizing the clinical presentations, radiological features, surgical treatment, and the possible mechanisms of hemorrhage in relevance to trochlear nerve schwannoma.

SUBMITTER: Lei J 

PROVIDER: S-EPMC9880228 | biostudies-literature | 2022

REPOSITORIES: biostudies-literature

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Publications

Hemorrhagic schwannoma of the trochlear nerve: Case report and a review of the literature.

Lei Jin J   Li Yu Y   Wan Xueyan X   Wang Junwen J   You Chao C   Zhao Kai K   Niu Hongquan H  

Frontiers in oncology 20230113


<h4>Background</h4>Schwannomas of the trochlear nerve with the absence of systemic neurofibromatosis are considerably uncommon, especially complicated by intra-tumoral hemorrhage. Due to the lack of typical clinical manifestations and imaging findings, a definite diagnosis of trochlear schwannomas before surgery is particularly difficult.<h4>Case presentation</h4>We report the case of a 64-year-old female patient who presented with a unilaterally intermittent headache of 2-month duration and wit  ...[more]

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