Publications by authors named "Shunsaku Takayanagi"

Ependymoma, a rare neuroepithelial malignancy of the central nervous system, affects both children and adults and may occur anywhere along the neuroaxis. This study aimed to analyze the treatment outcomes of adult intracranial ependymoma cases in Japan using data from the Brain Tumor Registry of Japan between 2001 and 2008. The dataset comprised 169 eligible patients after applying exclusion criteria, such as subependymoma and myxopapillary ependymoma cases.

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Gliomas, particularly IDH-wildtype ones, are associated with poor prognosis, yet their immunological landscape remains uncertain. We analyzed RNA sequencing data from 55 glioma patients, estimating immune infiltration with CIBERSORTx and immune cell states via Ecotyper. IDH-wildtype gliomas showed significantly higher immune cell infiltration ( = 0.

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To evaluate the therapeutic efficacy and safety of stereotactic radiosurgery (SRS) in the management of large cystic brain metastases. A retrospective analysis was conducted. Large cystic brain metastases were defined as cyst volume ≥ 5 mL.

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  • * Conducted from 2013 to 2021, the research included 10 patients, all of whom showed symptom improvement and a significant reduction in the size of the trapped ventricle, with no major complications reported during the procedure.
  • * The findings suggest that EVSP is a reliable and safer alternative to the traditional ventriculoperitoneal shunt (VPS) for treating TTH, emphasizing its potential to minimize risks associated with shunt failure and infection.
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Germ cell tumors (GCTs) are categorized as gonadal or extra-gonadal, based on the origin. Extra-gonadal GCTs predominantly manifest within the central nervous system (CNS), mediastinum, retroperitoneum, and sacrococcygeal region. These malignancies are most frequently diagnosed in the pediatric, adolescent, and young adult demographics.

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  • Recent cases suggest that high-grade supratentorial tumors in infants with specific ZFTA::NCOA1/2 fusions are categorized as ependymoma-like tumors with mesenchymal differentiation (ELTMDs).
  • This study presents a unique case in a 30-year-old woman showing mixed tumor components and a novel ZFTA::RELA fusion, differentiating it from traditional ependymomas.
  • The findings support classifying this case under ELTMD, marking it as the first adult instance analyzed through DNA methylation profiling, highlighting the potential recognition of ELTMD as a new type of tumor.
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  • * There is a risk that VPS can contribute to the spread of germinomas into the abdominal area, but the imaging characteristics of this complication are not well understood.
  • * This article presents the CT imaging findings related to the unusual but significant issue of diffuse peritoneal dissemination of intracranial germinoma.
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Introduction: Central neurocytoma (CN) is an extremely rare tumor primarily located in the supratentorial ventricular system, categorized as a glioneuronal or neuronal tumor.

Methods: This study presented a retrospective analysis of five CN patients who received adjuvant or salvage radiotherapy. Patients, aged 31-59 years, underwent radiation doses ranging from 60 Gy to 50.

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Surgical resection is considered for most brain tumors to obtain tissue diagnosis and to eradicate or debulk the tumor. Glioma, the most common primary malignant brain tumor, generally has a poor prognosis despite the multidisciplinary treatments with radical resection and chemoradiotherapy. Surgical resection of glioma is often complicated by the obscure border between the tumor and the adjacent brain tissues and by the tumor's infiltration into the eloquent brain.

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The majority of low-grade isocitrate dehydrogenase-mutant (IDH) gliomas undergo malignant progression (MP), but their underlying mechanism remains unclear. IDH gliomas exhibit global DNA methylation, and our previous report suggested that MP could be partly attributed to passive demethylation caused by accelerated cell cycles. However, during MP, there is also active demethylation mediated by ten-eleven translocation, such as DNA hydroxymethylation.

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  • The medulla oblongata is a rare site for germ cell tumors (GCTs) in the central nervous system, with limited data on their characteristics and outcomes.
  • A case study of a 24-year-old woman with vertigo and swallowing issues revealed a germinoma, which was surgically removed, followed by chemotherapy and irradiation, showing no recurrence after 4 months.
  • The literature suggests that GCTs in the medulla oblongata have similar prognosis to those in typical locations, with unique trends including higher age of occurrence, a female majority, and the significant risks associated with cardiac and respiratory functions.
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Background: Glioblastoma (GBM) is a highly lethal brain tumor. The effectiveness of temozolomide (TMZ) treatment in GBM is linked to the methylation status of O6-methyl-guanine DNA methyltransferase () promoter. Patients with unmethylated promoter have limited treatment options available.

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  • Ependymomas are diverse tumors with specific types based on where they occur and their molecular characteristics, with spinal ependymomas (SP-EPN) being the most common type found in the spinal cord of both children and adults.
  • Research revealed limited molecular data on SP-EPN, with known genetic changes including losses on chromosome 22q and mutations in NF2, but this study aimed to fill the gaps by analyzing transcriptomic, epigenetic, genetic, and clinical data from a large cohort.
  • The study identified two subtypes of SP-EPN: subtype A, associated with known NF2 mutations and more severe disease, and subtype B, characterized by different genetic alterations and more stable NF2 expression, helping to
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  • Spinal cord diffuse midline glioma, H3K27-altered, is a rare and serious type of tumor with unclear optimal treatment options.
  • A 76-year-old patient with symptoms of lower paralysis was diagnosed with this tumor, underwent initial surgery, and despite recurrence, achieved a positive outcome after a cordectomy procedure.
  • The study suggests that cordectomy could be beneficial for certain patients, particularly those with tumors located below the lower thoracic spine, in terms of better long-term survival.
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  • Researchers have learned a lot about meningiomas (a type of brain tumor), but there still isn't a specific treatment that targets their genetic make-up.
  • A recent case showed that even with advanced genetic testing, no targeted therapies were found to effectively treat the tumor's aggressive changes.
  • More studies are needed to understand the genetics of meningiomas better and create treatments that directly target these genetic changes.
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When managing cranial bone flap infections, infected bone flaps are typically removed and subsequently replaced with artificial bones 6 to 12 months after the inflammation subsides. However, defects in the occipital region pose challenges due to concerns regarding brain protection when patients lie in the supine position. Herein, the authors report the case of a 73-year-old woman with an occipital bone flap infection, which was successfully managed by reconstruction with a trapezius musculocutaneous flap immediately after removing the infected bone flap.

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Embryonal tumors with multilayered rosettes (ETMRs) are aggressive central nervous system (CNS) tumors that usually occur in young children. Here, we describe the first incidence of ETMR in an adult patient that also originated in the novel location of the internal auditory canal (IAC). The 36-year-old patient initially presented with unsteadiness, diplopia, and tinnitus.

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  • This study examines the characteristics of meningiomas in patients with neurofibromatosis type 2 (NF2), highlighting a long-term analysis of 159 tumors from 37 patients over approximately 13.5 years.
  • Findings indicate that meningiomas in NF2 patients are generally stable and show less aggressive behavior compared to sporadic meningiomas, with a higher prevalence of WHO grade I tumors.
  • Additionally, transcriptomic and immunohistochemical analyses reveal a stronger immune response in NF2 meningiomas, particularly with increased myeloid cell and macrophage infiltration, compared to sporadic NF2-altered meningiomas.
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  • Preoperative imaging plays a crucial role in planning treatment for brain metastasis, but it can sometimes be misleading, especially in patients receiving tyrosine kinase inhibitors (TKIs) like gefitinib for lung cancer.* -
  • The study analyzed 12 lung cancer cases with brain metastasis, including a notable instance where a patient on gefitinib showed atypical MRI and PET imaging characteristics, initially suggesting high-grade glioma instead of metastasis.* -
  • Findings indicate that TKIs may alter tumor behavior, leading to unusual imaging results; thus, it's essential to consider ongoing treatments when interpreting imaging for surgery planning.*
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Central neurocytoma (CN) is classically defined by its intraventricular location, neuronal/neurocytic differentiation, and histological resemblance to oligodendroglioma. Extraventricular neurocytoma (EVN) shares similar histological features with CN, while it distributes any site without contact with the ventricular system. CN and EVN have distinct methylation landscapes, and EVN has a signature fusion gene, FGFR1-TACC1.

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Purpose: Glioblastoma (GBM) is the most common type of primary malignant brain tumor and has a poor prognosis. Identifying novel targets and stratification strategies is urgently needed to improve patient survival. The present study aimed to identify clinically relevant genomic alterations in IDH-wildtype GBM using data from comprehensive genomic profiling (CGP) assays performed nationwide in Japan.

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Purpose: Leptomeningeal metastasis (LM) is a complication of surgery for brain metastasis and is a risk factor of poor prognosis. The risk of LM is particularly high after surgery for a breast cancer metastasis to the brain. If the risk of LM after surgical resection for a brain metastasis were predictable, appropriate adjuvant therapy could be administered to individual patients to improve their prognosis.

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Background: Lymphoproliferative disorder represents a heterogeneous clinicopathological spectrum characterized by uncontrolled proliferation of lymphocytes. Immunodeficiency is a major trigger of its development. While induction of immunodeficiency is a well-known adverse effect of temozolomide therapy, development of lymphoproliferative disorder following temozolomide therapy has not previously been described.

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Background: Glioblastoma is a malignant tumor, and its prognosis is as poor as 1.5 to 2 years. Most cases recur within one year even under the standard treatment.

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Synopsis of recent research by authors named "Shunsaku Takayanagi"

  • - Shunsaku Takayanagi's recent research focuses on various aspects of neurosurgery and neuro-oncology, investigating treatment options for brain tumors, the molecular characteristics of tumors, and complications arising from surgical interventions.
  • - His studies reveal innovative approaches such as neuroendoscopic techniques for treating trapped temporal horn and highlight genetic insights into tumors like glioblastoma and ependymomas, emphasizing the importance of molecular profiling for targeted therapies.
  • - Takayanagi’s work also addresses rare tumor presentations and complications, such as the peritoneal dissemination of intracranial germinomas and the implications of immunological factors in tumor aggressiveness, contributing valuable knowledge for improving patient outcomes in neurosurgical practice.