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 inWorld neurosurgery Vol. 95; pp. 516 - 524.e1
Main Authors Zhang, Si, Liang, Guopeng, Ju, Yan, You, Chao
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2016
Subjects
CT
MRI
DTI
GCT
AFP
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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.
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
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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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https://dx.doi.org/10.1016/j.wneu.2016.08.072
https://www.ncbi.nlm.nih.gov/pubmed/27567571
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Volume 95
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