A rare case of a combination of Dandy – Walker syndrome and large meningioma of the brain (clinical case)

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Authors: A.A. Chekhonatskiy, Maxim Valerievich Lymarev, V. I. Tsyganov, D. N. Filatov, Vladimir Andreevich Chekhonatsky
Cited by: 0
References: 9

Abstract

The article describes the experience of treating a 63-year-old patient with complete cerebellar atresia, Dandy – Walker syndrome in combination with a large meningioma of the brain. The Dandy – Walker malformation syndrome in its classical form includes: internal hydrocephalus of varying degrees; expansion of the III ventricle to the formation of a cyst of the posterior cranial fossa associated with upward displacement of the lateral sinuses and cerebellar namet; hypoplasia of the hemispheres and cerebellar worm. In 29–55 % of cases, Dandy – Walker syndrome is combined with other malformations (Meckel, Meckel – Gruber, Turner syndromes and other chromosomal aberrations), as well as with lesions of individual organs and systems (poly-, syndactyly, congenital heart defects, polycystic kidney disease, cleft palate). When analyzing modern literature, there was not a single described case of the occurrence of volumetric brain formation in combination with Dandy – Walker syndrome. The patient underwent surgical intervention with resection of the bone tissues of the skull, due to massive germination of the tumor tissue of the bones of the skull, total removal of the tumor. An increase in the number of described cases will make it possible to create algorithms for the diagnosis and treatment of this disease

Fields of Study & Subjects

Fetal and Pediatric Neurological Disorders Spinal Dysraphism and Malformations Meningioma and schwannoma management

Publication details

Journal / source
Российский нейрохирургический журнал им профессора А Л Поленова
Volume
17
Issue
4
Pages
148–154
Publication date
2 February 2026