2011
DOI: 10.1016/j.jmig.2010.09.002
|View full text |Cite
|
Sign up to set email alerts
|

Resolution of Catamenial Epilepsy after Goserelin Therapy and Oophorectomy: Case Report of Presumed Cerebral Endometriosis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
19
0

Year Published

2013
2013
2025
2025

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 16 publications
(20 citation statements)
references
References 7 publications
1
19
0
Order By: Relevance
“…As involvement of these nerves produces practically only non‐specific pelvic pain, it would not be feasible to provide a complete review of pelvic autonomic nervous system involvement. The literature search also revealed cases of catamenial headaches and epilepsy, and although in many EM can be suspected as a cause (Vilos et al, ), without histological confirmation they were not included.…”
Section: Methodsmentioning
confidence: 99%
“…As involvement of these nerves produces practically only non‐specific pelvic pain, it would not be feasible to provide a complete review of pelvic autonomic nervous system involvement. The literature search also revealed cases of catamenial headaches and epilepsy, and although in many EM can be suspected as a cause (Vilos et al, ), without histological confirmation they were not included.…”
Section: Methodsmentioning
confidence: 99%
“…The patient was thought to have cerebral endometriosis, a rare phenomenon that resulted in catamenial epilepsy. 10 Of course, this subject, is not related with the type of catamenial epilepsy presented in our report. Additional research is necessary to answer the question whether female sex hormones and sleep may engage interaction to produce catamenial-sleep epilepsy.…”
Section: Discussionmentioning
confidence: 44%
“…All neurological symptoms resolved completely after treatment with gonadotropin‐releasing hormone agonist for three months and subsequent laparoscopic bilateral oophorectomy. The patient was thought to have cerebral endometriosis, a rare phenomenon that resulted in catamenial epilepsy . Of course, this subject, is not related with the type of catamenial epilepsy presented in our report.…”
Section: Discussionmentioning
confidence: 50%
“…We considered also cerebral endometriosis, a rare complication of a rather frequent disease. Extrapelvic manifestations, such as gastrointestinal and genitourinary tracts, are widely known but single cases with brain lesions were also described [14,15]. In our case, no gynecological disorders were found.…”
Section: Discussionmentioning
confidence: 49%