Clinical and Radiologic Features of Pediatric Basal Ganglia Germ Cell Tumors
Pediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize the clinical features and radiological findings of this special subgroup of GCTs. From January 2010 to January 2015, 12 pediatric patients with basal ganglia GCTs were...
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Published in | World neurosurgery Vol. 95; pp. 516 - 524.e1 |
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Language | English |
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01.11.2016
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Abstract | Pediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize the clinical features and radiological findings of this special subgroup of GCTs.
From January 2010 to January 2015, 12 pediatric patients with basal ganglia GCTs were treated in our hospital. The clinical features, radiologic findings, diagnosis, treatment, and outcome of these patients were analyzed retrospectively. Our institutional diagnostic principle and treatment strategy of this disease were discussed.
GCTs accounted for 25.5% of all the pediatric basal ganglia tumors treated in our hospital. There were 9 male and 3 female patients with a mean age of 11.5 ± 2.1 years. The most common symptom was progressive hemiparesis (n = 9, 75%). The radiologic findings showed that the lesions predominately located in caput of caudate nucleus (n = 9, 75.0%), followed by lenticular nucleus (n = 3, 25.0%). Hemiatrophy was commonly observed (n = 8, 66.7%). Eight patients were diagnosed as having germinomas, and 4 patients as having nongerminomatous germ cell tumors. During the follow-up period, preoperative neurologic dysfunctions improved in 7 patients and remained stable in 3. Two patients developed new onset of neurologic dysfunction after the treatment. Two patients suffered from tumor recurrence.
GCTs are not as rare as considered in pediatric basal ganglia tumors. They bear some distinctive clinical and radiologic features, which can help with the accurate diagnosis and successful management of such tumors. |
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AbstractList | Pediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize the clinical features and radiological findings of this special subgroup of GCTs.
From January 2010 to January 2015, 12 pediatric patients with basal ganglia GCTs were treated in our hospital. The clinical features, radiologic findings, diagnosis, treatment, and outcome of these patients were analyzed retrospectively. Our institutional diagnostic principle and treatment strategy of this disease were discussed.
GCTs accounted for 25.5% of all the pediatric basal ganglia tumors treated in our hospital. There were 9 male and 3 female patients with a mean age of 11.5 ± 2.1 years. The most common symptom was progressive hemiparesis (n = 9, 75%). The radiologic findings showed that the lesions predominately located in caput of caudate nucleus (n = 9, 75.0%), followed by lenticular nucleus (n = 3, 25.0%). Hemiatrophy was commonly observed (n = 8, 66.7%). Eight patients were diagnosed as having germinomas, and 4 patients as having nongerminomatous germ cell tumors. During the follow-up period, preoperative neurologic dysfunctions improved in 7 patients and remained stable in 3. Two patients developed new onset of neurologic dysfunction after the treatment. Two patients suffered from tumor recurrence.
GCTs are not as rare as considered in pediatric basal ganglia tumors. They bear some distinctive clinical and radiologic features, which can help with the accurate diagnosis and successful management of such tumors. Background and Objective Pediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize the clinical features and radiological findings of this special subgroup of GCTs. Methods From January 2010 to January 2015, 12 pediatric patients with basal ganglia GCTs were treated in our hospital. The clinical features, radiologic findings, diagnosis, treatment, and outcome of these patients were analyzed retrospectively. Our institutional diagnostic principle and treatment strategy of this disease were discussed. Results GCTs accounted for 25.5% of all the pediatric basal ganglia tumors treated in our hospital. There were 9 male and 3 female patients with a mean age of 11.5 ± 2.1 years. The most common symptom was progressive hemiparesis ( n = 9, 75%). The radiologic findings showed that the lesions predominately located in caput of caudate nucleus ( n = 9, 75.0%), followed by lenticular nucleus ( n = 3, 25.0%). Hemiatrophy was commonly observed ( n = 8, 66.7%). Eight patients were diagnosed as having germinomas, and 4 patients as having nongerminomatous germ cell tumors. During the follow-up period, preoperative neurologic dysfunctions improved in 7 patients and remained stable in 3. Two patients developed new onset of neurologic dysfunction after the treatment. Two patients suffered from tumor recurrence. Conclusions GCTs are not as rare as considered in pediatric basal ganglia tumors. They bear some distinctive clinical and radiologic features, which can help with the accurate diagnosis and successful management of such tumors. BACKGROUND AND OBJECTIVEPediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize the clinical features and radiological findings of this special subgroup of GCTs.METHODSFrom January 2010 to January 2015, 12 pediatric patients with basal ganglia GCTs were treated in our hospital. The clinical features, radiologic findings, diagnosis, treatment, and outcome of these patients were analyzed retrospectively. Our institutional diagnostic principle and treatment strategy of this disease were discussed.RESULTSGCTs accounted for 25.5% of all the pediatric basal ganglia tumors treated in our hospital. There were 9 male and 3 female patients with a mean age of 11.5 ± 2.1 years. The most common symptom was progressive hemiparesis (n = 9, 75%). The radiologic findings showed that the lesions predominately located in caput of caudate nucleus (n = 9, 75.0%), followed by lenticular nucleus (n = 3, 25.0%). Hemiatrophy was commonly observed (n = 8, 66.7%). Eight patients were diagnosed as having germinomas, and 4 patients as having nongerminomatous germ cell tumors. During the follow-up period, preoperative neurologic dysfunctions improved in 7 patients and remained stable in 3. Two patients developed new onset of neurologic dysfunction after the treatment. Two patients suffered from tumor recurrence.CONCLUSIONSGCTs are not as rare as considered in pediatric basal ganglia tumors. They bear some distinctive clinical and radiologic features, which can help with the accurate diagnosis and successful management of such tumors. |
Author | You, Chao Zhang, Si Ju, Yan Liang, Guopeng |
Author_xml | – sequence: 1 givenname: Si surname: Zhang fullname: Zhang, Si organization: Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China – sequence: 2 givenname: Guopeng surname: Liang fullname: Liang, Guopeng organization: Intensive Care Unit, West China Hospital of Sichuan University, Chengdu, Sichuan, China – sequence: 3 givenname: Yan surname: Ju fullname: Ju, Yan email: juyan4022@sina.com organization: Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China – sequence: 4 givenname: Chao surname: You fullname: You, Chao organization: Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27567571$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1007/BF00262257 10.1007/s00381-007-0495-2 10.1007/s00247-005-0063-4 10.1186/s40644-014-0035-8 10.1007/s00234-001-0735-1 10.1007/BF01053275 10.1007/s00062-015-0380-4 10.3171/jns.1998.88.1.0126 10.1016/S1470-2045(15)00244-2 10.3171/2010.5.PEDS09112 10.3171/2009.7.PEDS08288 10.1007/s00234-001-0752-0 10.1159/000083745 10.1002/cncr.11495 10.1007/s11912-014-0393-1 10.1007/s00234-015-1553-1 10.1016/S1726-4901(10)70096-4 10.1259/bjr/25001856 10.1634/theoncologist.2008-0037 10.1016/S0887-8994(98)00161-1 10.1007/s00381-008-0787-1 10.1007/s00701-015-2614-2 10.1007/BF00588516 10.1097/NRL.0b013e31820ba6c0 10.1007/s003810050366 10.1007/s002340050634 |
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Keywords | Germ cell tumor CT Basal ganglia NGGCT AT/RT MRI DTI PNET β-HCG GCT AFP Pediatric Primitive neuroectodermal tumor Atypical teratoid/rhabdoid tumor β-human chorionic gonadotropin Alpha-fetoprotein Diffusion tensor imaging Computed tomography Magnetic resonance imaging Nongerminomatous germ cell tumor |
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Snippet | Pediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize the clinical features and... Background and Objective Pediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize... BACKGROUND AND OBJECTIVEPediatric basal ganglia germ cell tumors (GCTs) represent a rare subset of tumors about which little is known. We aimed to summarize... |
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SubjectTerms | Adolescent Aftercare alpha-Fetoproteins - metabolism Antineoplastic Combined Chemotherapy Protocols - therapeutic use Basal ganglia Basal Ganglia Diseases - complications Basal Ganglia Diseases - diagnostic imaging Basal Ganglia Diseases - metabolism Basal Ganglia Diseases - therapy Brain Neoplasms - complications Brain Neoplasms - diagnostic imaging Brain Neoplasms - metabolism Brain Neoplasms - therapy Carboplatin - administration & dosage Carcinoma, Embryonal - complications Carcinoma, Embryonal - diagnostic imaging Carcinoma, Embryonal - metabolism Carcinoma, Embryonal - therapy Caudate Nucleus - diagnostic imaging Caudate Nucleus - surgery Child Choriocarcinoma, Non-gestational - complications Choriocarcinoma, Non-gestational - diagnostic imaging Choriocarcinoma, Non-gestational - metabolism Choriocarcinoma, Non-gestational - therapy Chorionic Gonadotropin, beta Subunit, Human - metabolism Cisplatin - administration & dosage Cognitive Dysfunction - etiology Corpus Striatum - diagnostic imaging Corpus Striatum - surgery Cranial Irradiation Diffusion Tensor Imaging Endodermal Sinus Tumor - complications Endodermal Sinus Tumor - diagnostic imaging Endodermal Sinus Tumor - metabolism Endodermal Sinus Tumor - therapy Etoposide - administration & dosage Female Germ cell tumor Germinoma - complications Germinoma - diagnostic imaging Germinoma - metabolism Germinoma - therapy Humans Magnetic Resonance Imaging Male Neoadjuvant Therapy Neoplasms, Germ Cell and Embryonal - complications Neoplasms, Germ Cell and Embryonal - diagnostic imaging Neoplasms, Germ Cell and Embryonal - metabolism Neoplasms, Germ Cell and Embryonal - therapy Neurosurgery Neurosurgical Procedures Paresis - etiology Pediatric Retrospective Studies Second-Look Surgery Seizures - etiology Tomography, X-Ray Computed |
Title | Clinical and Radiologic Features of Pediatric Basal Ganglia Germ Cell Tumors |
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