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Symptomatic xanthogranuloma of the lateral ventricle in a pregnant patient treated with delayed resection: A case report and systematic review.

Abstract：

:Intracranial xanthogranulomas (XG) are a rare benign histiocytic neoplasm and most often within the choroid. The majority are asymptomatic and are found incidentally on imaging or post-mortem examination or autopsy. We present a case of symptomatic XG in a pregnant patient who underwent a delayed transcortical, transventricular approach for lateral ventricle XG resection following the completion of her pregnancy. Four years post-operatively, the patient is neurologically intact and without recurrence. Our review of the literature showed differences among XG depending on location. The clinical and radiological features of XG are often indistinguishable from tumors arising from the choroid plexus and should be considered as a rare etiology in the differential of newly diagnosed intraventricular lesions.

journal_name

Clin Neurol Neurosurg

journal_title

Clinical neurology and neurosurgery

authors

Mathkour M,Michael A,Scullen T,Carsky K,Hage M,Werner C,Carr C,Keen JR,Ware ML

doi

10.1016/j.clineuro.2020.106143

subject

Has Abstract

pub_date

2020-11-01 00:00:00

pages

106143

eissn

0303-8467

issn

1872-6968

pii

S0303-8467(20)30486-8

journal_volume

198

pub_type

杂志文章,评审

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