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[Giant cavernous malformation of the genu of the corpus callosum].

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Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko 📖 저널 OA 0% 2021: 0/1 OA 2022: 0/7 OA 2023: 0/4 OA 2024: 0/5 OA 2025: 0/2 OA 2026: 0/9 OA 2021~2026 2026 Vol.90(1) p. 92-99
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
total resection of malformation
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Elements of Korsakoff syndrome persisted with improvements under rehabilitation sessions with neuropsychologist. [CONCLUSION] Despite difficult anatomical location and giant size, total resection of cavernous malformation provided satisfactory outcome with minimal neurological complications.

Chizhova KA, Mavlyutova RR, Vinnikov VM, Belov IY, Gulyaev DA

📝 환자 설명용 한 줄

[UNLABELLED] Cavernous malformations of the corpus callosum are rare accounting for less than 1% of all subtentorial cavernous malformations.

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APA Chizhova KA, Mavlyutova RR, et al. (2026). [Giant cavernous malformation of the genu of the corpus callosum].. Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko, 90(1), 92-99. https://doi.org/10.17116/neiro20269001192
MLA Chizhova KA, et al.. "[Giant cavernous malformation of the genu of the corpus callosum].." Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko, vol. 90, no. 1, 2026, pp. 92-99.
PMID 41668579 ↗

Abstract

[UNLABELLED] Cavernous malformations of the corpus callosum are rare accounting for less than 1% of all subtentorial cavernous malformations. Clinical manifestations are usually caused by hemorrhage into adjacent parenchyma. Epileptic seizures are the most common. Multiple hemorrhages with progressive neurological impairment require surgical intervention.

[OBJECTIVE] To present giant cavernoma of the genu of the corpus callosum extending to the fornix, basal frontal lobes and bottom of the third ventricle, as well as review of available literature.

[RESULTS] A patient with giant cavernous malformation of the genu of the corpus callosum extending to the fornix, basal frontal lobes and bottom of the third ventricle underwent total resection of malformation. Symptoms included headaches, epileptic seizures, and hydrocephalus. Korsakoff syndrome developed after surgery and partially regressed at discharge. After 3 months, hydrocephalus completely regressed. Elements of Korsakoff syndrome persisted with improvements under rehabilitation sessions with neuropsychologist.

[CONCLUSION] Despite difficult anatomical location and giant size, total resection of cavernous malformation provided satisfactory outcome with minimal neurological complications.

🏷️ 키워드 / MeSH 📖 같은 키워드 OA만

🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반