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Adult cerebral high-grade glioneuronal tumor with perivascular or pseudopapillary growth co-existing with low-grade tumor: a case report

International journal of clinical and experimental pathology, 2023, Vol.16 (10), p.294-302

2023

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Systemic Metastasis of Pediatric Diffuse High-grade Astrocytoma: A Case Report

NMC case report journal, 2023, Vol.10, p.265-271

2023

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SEGA-like circumscribed astrocytoma in a non-NF1 patient, harboring molecular profile of GBM. A case report

Neuropathology : official journal of the Japanese Society of Neuropathology, 2024, Vol.44 (3), p.190-199

2024

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Thoracic Intra and Extramedullary Capillary Hemangioma with Subacute Clinical Course: A Case Report and Literature Review

NMC case report journal, 2024, Vol.11, p.85-91

2024

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Oozing-type rupture caused by right ventricular intramural hematoma after right ventricular infarction

Journal of cardiology cases, 2022, Vol.26 (6), p.395-398

2022

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Polygenic variants related to familial hypobetalipoproteinemia in a patient with Alzheimer's disease homozygotic for the APOE ε2 allele presenting multiple cortical superficial siderosis and recurrent lobar hemorrhages

Neurogenetics, 2022, Vol.23 (1), p.69-71

2022

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IgG4-Related Disease in the Frontal Convexity Concomitant with Smoldering Multiple Myeloma: A Case Report and Review of the Literature Regarding Therapeutic Implications

World neurosurgery, 2020, Vol.143, p.247-260

2020

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An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis

Neuropathology : official journal of the Japanese Society of Neuropathology, 2022, Vol.42 (3), p.190-196

2022

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Increased Twist and ZEB2 expression in a cutaneous metastasis of high-grade glioma

Neuropathology : official journal of the Japanese Society of Neuropathology, 2020, Vol.40 (2), p.196-201

2020

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Clinicopathological and Genomic Features of Pediatric Intracranial Myxoid Mesenchymal Tumor with both of EWSR1-CREM Gene Fusion and MAP3K13 Mutation: A Case Report and Comparison with Adult Cases in the Literature

NMC case report journal, 2022, Vol.9, p.101-109

2022

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An Adult Case of Sellar Atypical Teratoid/Rhabdoid Tumor Presenting with Lung Metastasis, Harboring a Compound Heterozygous Mutation in INI1

NMC case report journal, 2021, Vol.8 (1), p.267-274

2021

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Oligodendroglioma showing pleomorphic xanthoastrocytoma-like perivascular microlesion: With IDH1, TERT promoter mutation and 1p/19q codeletion detected in both components

Pathology international, 2020, Vol.70 (1), p.40-46

2020

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The first reported case of Noonan syndrome complicated with hepatocellular carcinoma

Clinical case reports, 2021, Vol.9 (7), p.e04317-e04317

2021

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Cerebellar high-grade astrocytoma with IDH mutations in the elderly: A report of two cases

Neuropathology : official journal of the Japanese Society of Neuropathology, 2018

2018

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Gliosarcoma with primitive neuronal, chondroid, osteoid and ependymal elements

Neuropathology : official journal of the Japanese Society of Neuropathology, 2018

2018

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Anaplastic ganglioglioma with epithelioid cell components

Neuropathology : official journal of the Japanese Society of Neuropathology, 2018, Vol.38 (5), p.498-502

2018

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An epilepsy-associated glioneuronal tumor with mixed morphology harboring FGFR1 mutation

Pathology international, 2019, Vol.69 (6), p.372-377

2019

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Concurrent TERT promoter and BRAF V600E mutation in epithelioid glioblastoma and concomitant low-grade astrocytoma

Neuropathology : official journal of the Japanese Society of Neuropathology, 2017, Vol.37 (1), p.58-63

2017

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Genetic mutations in high grade gliomas of the adult spinal cord

Brain tumor pathology, 2016, Vol.33 (4), p.267-269

2016

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Dentatorubral-pallidoluysian atrophy (DRPLA) with a small ganglioglioma component containing neurofibrillary tangles and polyglutamine aggregation

Neuropathology : official journal of the Japanese Society of Neuropathology, 2017, Vol.37 (4), p.335-340

2017

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A case of high-grade astrocytoma with BRAF and ATRX mutations following a long-standing course over two decades

Neuropathology : official journal of the Japanese Society of Neuropathology, 2017, Vol.37 (4), p.351-357

2017

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Accumulation of periostin in acute exacerbation of familial idiopathic pulmonary fibrosis

Journal of thoracic disease, 2018, Vol.10 (7), p.E587-E591

2018

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The Feature of Solitary Small Nodular Type of Hepatic Epithelioid Hemangioendothelioma

Case reports in gastroenterology, 2018, Vol.12 (2), p.402-410

2018

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Myeloid sarcoma arising in malignant phyllodes tumour: clonal relationships revealed by comparative genome-wide analyses

British journal of haematology, 2018, Vol.181 (2), p.255-259

2018

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Adult cerebral high-grade glioneuronal tumor with perivascular or pseudopapillary growth co-existing with low-grade tumor: a case report

Systemic Metastasis of Pediatric Diffuse High-grade Astrocytoma: A Case Report

SEGA-like circumscribed astrocytoma in a non-NF1 patient, harboring molecular profile of GBM. A case report

Thoracic Intra and Extramedullary Capillary Hemangioma with Subacute Clinical Course: A Case Report and Literature Review

Oozing-type rupture caused by right ventricular intramural hematoma after right ventricular infarction

Polygenic variants related to familial hypobetalipoproteinemia in a patient with Alzheimer's disease homozygotic for the APOE ε2 allele presenting multiple cortical superficial siderosis and recurrent lobar hemorrhages

IgG4-Related Disease in the Frontal Convexity Concomitant with Smoldering Multiple Myeloma: A Case Report and Review of the Literature Regarding Therapeutic Implications

An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis

Increased Twist and ZEB2 expression in a cutaneous metastasis of high-grade glioma

Clinicopathological and Genomic Features of Pediatric Intracranial Myxoid Mesenchymal Tumor with both of EWSR1-CREM Gene Fusion and MAP3K13 Mutation: A Case Report and Comparison with Adult Cases in the Literature

An Adult Case of Sellar Atypical Teratoid/Rhabdoid Tumor Presenting with Lung Metastasis, Harboring a Compound Heterozygous Mutation in INI1

Oligodendroglioma showing pleomorphic xanthoastrocytoma-like perivascular microlesion: With IDH1, TERT promoter mutation and 1p/19q codeletion detected in both components

The first reported case of Noonan syndrome complicated with hepatocellular carcinoma

Cerebellar high-grade astrocytoma with IDH mutations in the elderly: A report of two cases

Gliosarcoma with primitive neuronal, chondroid, osteoid and ependymal elements

Anaplastic ganglioglioma with epithelioid cell components

An epilepsy-associated glioneuronal tumor with mixed morphology harboring FGFR1 mutation

Concurrent TERT promoter and BRAF V600E mutation in epithelioid glioblastoma and concomitant low-grade astrocytoma

Recurrent Lobar Hemorrhages and Multiple Cortical Superficial Siderosis in a Patient of Alzheimer's Disease With Homozygous APOE ε2 Allele Presenting Hypobetalipoproteinemia and Pathological Findings of 18F-THK5351 Positron Emission Tomography: A Case Report

Genetic mutations in high grade gliomas of the adult spinal cord

Dentatorubral-pallidoluysian atrophy (DRPLA) with a small ganglioglioma component containing neurofibrillary tangles and polyglutamine aggregation

A case of high-grade astrocytoma with BRAF and ATRX mutations following a long-standing course over two decades

Accumulation of periostin in acute exacerbation of familial idiopathic pulmonary fibrosis

The Feature of Solitary Small Nodular Type of Hepatic Epithelioid Hemangioendothelioma

Myeloid sarcoma arising in malignant phyllodes tumour: clonal relationships revealed by comparative genome-wide analyses

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