Meningioma

A rare, mostly benign, primary tumor of the meninges (arachnoid cap cells), usually located in the supratentorial compartment, commonly appearing in the sixth and seventh decade of life, clinically silent in most cases or causing hyperostosis close to the tumor and resulting in focal bulging and localized pain in less than 10% of cases. Additional features may include headache, seizures, gradual personality changes (apathy and dementia), anosmia, impaired vision, exophthalmos, hearing loss, ataxia, dysmetria, hypotonia, nystagmus, and rarely spontaneous bleeding.

Primary amenorrhea

Total: 2

(per page)

PMID (PMCID)
31149308	OTHER
	THE RARE CASE OF MIXED GONADAL DYSGENESIS, MOSAIC KARYOTYPE, PETROCLIVAL MENINGIOMA AND IDIOPATHIC HYPERDEHYDROEPIANDROSTERONISM.
	Matulevicius V, Urbanavicius V, Lukosevicius S, Ciaplinskiene L, Ostrauskas R. Acta Endocrinol (Buchar). 2018;14(4):527-532.
	The case of a 37-year-old woman mosaic karyotype - 45,X/46,XY, infertility, virilisation, Turner syndrome-like phenotype, primary amenorrhea, the absence of labia majora and petroclival meningioma.
1508293	FEMALE	Adult
	Convexity meningioma associated with empty sella presenting as primary amenorrhea.
	von Wild K, Hobik HP, Kulali A. Neurochirurgia (Stuttg). 1992;35(4):127-30.
	Convexity meningioma associated with empty sella presenting as primary amenorrhea.