2.A Case of Basilar Groove Meningioma in a Child.
Sung Nam HWANG ; Young Cho KOH ; Byung Kyu CHO ; Bo Sung SIM ; Je G CHI ; Tae Dong PARK
Journal of Korean Neurosurgical Society 1979;8(2):339-344
Meningeal tumor obstructing the foramen magnum is relatively rare, moreover occurrence of such a tumor in children has rarely been reported. This tumor shows various characteristic clinical manifestations, partly from anatomical standpoint and partly from unknown mechanism. In addition, not uncommon remitting and relapsing clinical course often presents diagnostic conflicts. We experienced a case of basilar groove meningioma presenting many difficult problems in the diagnosis and treatment, which was confirmed at operation and subsequent autopsy in a child.
Autopsy
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Child*
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Diagnosis
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Foramen Magnum
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Humans
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Meningeal Neoplasms
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Meningioma*
4.Molecular diagnosis and treatment of meningiomas: an expert consensus (2022).
Jiaojiao DENG ; Lingyang HUA ; Liuguan BIAN ; Hong CHEN ; Ligang CHEN ; Hongwei CHENG ; Changwu DOU ; Dangmurenjiapu GENG ; Tao HONG ; Hongming JI ; Yugang JIANG ; Qing LAN ; Gang LI ; Zhixiong LIU ; Songtao QI ; Yan QU ; Songsheng SHI ; Xiaochuan SUN ; Haijun WANG ; Yongping YOU ; Hualin YU ; Shuyuan YUE ; Jianming ZHANG ; Xiaohua ZHANG ; Shuo WANG ; Ying MAO ; Ping ZHONG ; Ye GONG
Chinese Medical Journal 2022;135(16):1894-1912
ABSTRACT:
Meningiomas are the most common primary intracranial neoplasm with diverse pathological types and complicated clinical manifestations. The fifth edition of the WHO Classification of Tumors of the Central Nervous System (WHO CNS5), published in 2021, introduces major changes that advance the role of molecular diagnostics in meningiomas. To follow the revision of WHO CNS5, this expert consensus statement was formed jointly by the Group of Neuro-Oncology, Society of Neurosurgery, Chinese Medical Association together with neuropathologists and evidence-based experts. The consensus provides reference points to integrate key biomarkers into stratification and clinical decision making for meningioma patients.
REGISTRATION
Practice guideline REgistration for transPAREncy (PREPARE), IPGRP-2022CN234.
Humans
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Meningioma/pathology*
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Consensus
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Neurosurgical Procedures
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Meningeal Neoplasms/pathology*
6.Intraoperative radiation therapy as an adjunctive therapy for huge and highly vascular parasagittal meningiomas.
Tae Hyung CHO ; Yong Gu CHUNG ; Chul Yong KIM ; Han Kyeom KIM ; Nam Joon LEE ; Jeong Wha CHU ; Myung Sun CHOI
Journal of Korean Medical Science 2000;15(6):718-723
This case presents a 34-year-old man who had a huge parasagittal meningioma. Initial treatment consisted of preoperative external carotid artery embolization and partial tumor resection. During the resection, we found that the tumor invaded the adjacent calvarium, and due to massive hemorrhage, total removal of the tumor was impossible. The patient was treated with intraoperative radiation therapy (IORT) (25 Gy via 16 MeV) as an adjunctive therapy. Eight months after IORT, we were able to remove the tumor completely without surgical difficulties. IORT can be considered an useful adjunctive therapy for the superficially located, huge, and highly vascular meningioma.
Adult
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Journal Article
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Human
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Intraoperative Care*
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Magnetic Resonance Imaging
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Male
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Meningeal Neoplasms/surgery
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Meningeal Neoplasms/radiotherapy*
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Meningeal Neoplasms/pathology
;
Meningioma/surgery
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Meningioma/radiotherapy*
;
Meningioma/pathology
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Vascular Neoplasms/surgery
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Vascular Neoplasms/radiotherapy*
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Vascular Neoplasms/pathology
9.Guillain-Barre syndrome complicated on post-operation with renal carcinoma and meningioma: a case report.
Shuai XU ; Yang Shuo WANG ; Shu LI ; Hai Ying LIU
Journal of Peking University(Health Sciences) 2019;51(4):775-777
Guillain-Barre syndrome (GBS) is an autoimmune disease on the injury of peripheral nerve myelin proteins or axon, of which the acute motor axonal neuropathy (AMAN) as a subtype is of infrequence and an extremely low incidence of post-operation. This article originally reported one case from Peking University People's Hospital on successful treatment of severe GBS (AMAN) on post-operation with renal carcinoma and meningioma. The diagnostic criteria of AMAN refer to AIDP, of which the feature of AMAN suggests a pure motor nerve dysfunction and significant damage on motor axon. It is reported that infection and surgery may induce GBS. The positive result of IgM and IgG was considered the application of ganglioside and blood-brain barrier might be damaged after meningioma surgery which eased the drug to enter the cerebrospinal fluid circulation and induced lesions, therefore the etiology on this GBS case was of high confidence of administrating ganglioside drugs. Autonomic nerve dysfunctions, such as blood pressure fluctuations and arrhythmia could be caused in GBS, of which about 3%-10% of GBS patients would die. Early use of gamma globulin or plasma exchange was recommended internationally, but recently some new ideas, to some extent, of significance on GBS treatment emerged. However, there was still no consensus on GBS treatment systematically all over the world. Till now, the general treatment program on GBS may be still gamma globulin or plasma exchange and a curious judgment of prognosis is essential in order to make a reasonable plan. That it was usually of no omen on severe autonomic nerve dysfunction must be successively monitored, the same as the management of the respiratory tract and nutrition support. The key measures taken on lung recruitment was postural drainage on this case with a low cost but a qualified effectiveness. This case report aimed to deepen the understanding of AMAN and acquaint the cutting-edge advances on the treatment of GBS, as well as providing successful treatment experience for the prevention on similar cases.
Carcinoma, Renal Cell
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Guillain-Barre Syndrome
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Humans
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Kidney Neoplasms
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Meningeal Neoplasms
;
Meningioma
10.Cytogenetic analysis of meningiomas.
Jeong Hee CHO ; Gyeong Yeob GONG ; Eun Sil YU ; Chung Jin WHANG ; Kwan Ja JEE ; In Chul LEE
Journal of Korean Medical Science 1992;7(2):162-166
Cytogenetic analysis of 4 cases of meningiomas from 3 male and 1 female patients is reported. One of male patients suffered from neurofibromatosis type 2. Histologically, the meningiomas were meningotheliomatous (1), transitional (2), and psammomatous (1). Chromosomal abnormalities were found in all cases with a karyotype 45,XY,-22, 45,XY,-16, 45,XX,-2, and 45,XY,t (15p;22q), respectively. Monosomy of chromosome 22 was detected only in the patient with neurofibromatosis type 2. These cytogenetic analysis demonstrates that variable clonal karyotype aberrations exist in meningiomas.
Adolescent
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Adult
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*Chromosome Aberrations
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Female
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Humans
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Male
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Meningeal Neoplasms/*genetics
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Meningioma/*genetics
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Neurofibromatosis 2/genetics