Multiple faces of children and juvenile meningiomas: A report of single-center experience and review of literature

被引:17
作者
Stanuszek, Agnieszka [1 ]
Piatek, Paula [1 ]
Kwiatkowski, Stanislaw [2 ]
Adamek, Dariusz [3 ]
机构
[1] Jagiellonian Univ, Coll Med, Univ Childrens Hosp, Students Res Grp,Dept Neurosurg, Krakow, Poland
[2] Jagiellonian Univ, Coll Med, Univ Childrens Hosp, Dept Neurosurg, Krakow, Poland
[3] Jagiellonian Univ, Coll Med, Chair Pathomorphol, Dept Neuropathol, Krakow, Poland
关键词
Meningioma; Pediatric brain tumors; Neurofibromatosis type 2; Pediatric meningiomas; CUTANEOUS PLEXIFORM SCHWANNOMAS; GERM-LINE MUTATIONS; OF-THE-LITERATURE; NEUROFIBROMATOSIS TYPE-2; CLINICAL-FEATURES; INTRACRANIAL MENINGIOMAS; PEDIATRIC MENINGIOMAS; NATURAL-HISTORY; NF2; CHILDHOOD;
D O I
10.1016/j.clineuro.2013.12.019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Pediatric meningiomas are extremely rare tumors often associated with various medical conditions. This report is an attempt to analyze the clinical behavior, pathological presentation and recommended management of both isolated and neurofibromatosis type 2 (NF2) related pediatric meningiomas in comparison to their adult counterparts. Methods: The investigated group consisted of three male and six female patients suffering from meningiomas of the central nervous system, who were hospitalized at our department in years 2001-2012. Results: In our group three children were diagnosed with NF2. Two were released with a suspicion of that disease. Three patients had multiple meningiomas at the first presentation. The most common manifestation were focal neurological deficits (47%). Meningiomas were mostly located at the brain convexity (29%). Histological examination revealed the domination of fibrous type in our group (29%). Apart from surgical management a preoperative embolization of the tumors' vessels was implemented in two children. Another three children underwent postoperative radiotherapy (RTh), one received a chemotherapy (ChTh). Conclusion: Meningiomas in children differ from their counterparts in adults. Due to common coexistence of pediatric meningiomas and neurofibromatosis type 2, this group of patients should be taken under strict control, because of high risk of tumor recurrence. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 75
页数:7
相关论文
共 47 条
[1]   Intracranial meningiomas in children [J].
Alexiou, George A. ;
Mpairamidis, Evriviadis ;
Psarros, Antonios ;
Sfakianos, George ;
Prodromou, Neofytos .
PEDIATRIC NEUROSURGERY, 2008, 44 (05) :373-375
[2]   Meningiomas of the central nervous system occurring below the age of 17: report of 24 cases not associated with neurofibromatosis and review of literature [J].
Amirjamshidi, A ;
Mehrazin, M ;
Abbassioun, K .
CHILDS NERVOUS SYSTEM, 2000, 16 (07) :406-415
[3]  
[Anonymous], 2010, CBTRUS STAT REP PRIM
[4]   Pediatric intracranial meningiomas - Do they differ from their counterparts in adults? [J].
Arivazhagan, A. ;
Devi, B. Indira ;
Kolluri, Sastry V. R. ;
Abraham, R. G. ;
Sampath, S. ;
Chandramouli, B. A. .
PEDIATRIC NEUROSURGERY, 2008, 44 (01) :43-48
[5]   Plexiform schwannoma: a clinicopathologic overview with emphasis on the head and neck region [J].
Berg, Jena C. ;
Scheithauer, Bernd W. ;
Spinner, Robert J. ;
Allen, Carl M. ;
Koutlas, Ioannis G. .
HUMAN PATHOLOGY, 2008, 39 (05) :633-640
[6]   Multiple cutaneous plexiform schwannomas revealing neurofibromatosis type 2 in a child - report of a novel mutation in this rare association [J].
Cruz, Maria Joao ;
Baudrier, Teresa ;
Gil-Da-Costa, Maria Joao ;
Azevedo, Filomena ;
Mota, Alberto .
EUROPEAN JOURNAL OF DERMATOLOGY, 2011, 21 (06) :1010-1011
[7]   Meningiomas in childhood [J].
Di Rocco, C ;
Di Rienzo, A .
CRITICAL REVIEWS IN NEUROSURGERY, 1999, 9 (03) :180-188
[8]   Long-term natural history of neurofibromatosis Type 2-associated intracranial tumors Clinical article [J].
Dirks, Michael S. ;
Butman, John A. ;
Kim, H. Jeffrey ;
Wu, Tianxia ;
Morgan, Keaton ;
Tran, Anne P. ;
Lonser, Russell R. ;
Asthagiri, Ashok R. .
JOURNAL OF NEUROSURGERY, 2012, 117 (01) :109-117
[9]  
Edringer P, 1998, SURG NEUROL, V49, P136
[10]   Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma? [J].
Evans, D. G. R. ;
Ramsden, R. T. ;
Gokhale, C. ;
Bowers, N. ;
Huson, S. M. ;
Wallace, A. .
CLINICAL GENETICS, 2007, 71 (04) :354-358