Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 2005 · 67 citations · 36 references
MedicineObstetricsOncologyEndocrine OncologyMaternal-fetal MedicineReproductive EndocrinologyGonadal HormonesHormonal Cancer TherapyHormonal EvaluationHormonal TherapyPregnancyPregnancy Loss PathologyEstrogen Receptor SignalingGrowth Factor-receptor InteractionsMeningioma PathologyMeningioma RecurrencePlatelet-derived Growth Factor ReceptorsProgesterone Receptor ExpressionProgesterone Receptor SignalingProgesterone Receptor Status
BACKGROUND: Increased growth of meningiomas during pregnancy as well as postpartum clinical regression of symptoms have been reported but remain poorly understood. A better understanding of the factors that contribute to these observations, including potential factors associated with pregnancy, could enable design of more effective adjuvant therapies. METHODS: We describe the presentation of a meningioma during the immediate postpartum period. Serial imaging demonstrated subsequent rapid decrease in size of the tumour prior to any intervention. The lesion was resected, and the tissue was subjected to immunostaining for gene products associated with pregnancy, including estrogen receptor (ER), progesterone receptor (PR), platelet-derived growth factor receptor B (PDGFRB), fibroblastic growth factor receptor 2 (FGFR-2), epidermal growth factor receptor (EGFR) and human placental lactogen (hPL). RESULTS: The lesion proved to be an atypical fibroblastic meningioma grade II (WHO). Immunostaining demonstrated significant staining for PR, PDGFRB, and FGFR-2. No specific staining for ER, EGFR, or hPL was identified. CONCLUSION: Although clinical regression of meningioma following pregnancy is well-recognized, imaging data are much less abundant. This report provides clear clinical and imaging documentation of a meningioma associated with pregnancy. In addition, the growth factor profile of this tumour suggests the importance of PR, PDGFRB, and FGFR-2 as potential therapeutic targets.
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Nervous system neoplasms and primary malignancies of other sites
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