Neuropathology

Papers
(The median citation count of Neuropathology is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-06-01 to 2025-06-01.)
ArticleCitations
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Associations of late‐life blood pressure with CERAD, Braak, and Thal: Findings from the National Alzheimer's coordinating center neuropathology dataset14
Neurolymphomatosis in follicular lymphoma: an autopsy case report13
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor13
The neostriatum in polyglutamine diseases: preferential decreases in large neurons in dentatorubral‐pallidoluysian atrophy and Machado‐Joseph disease and in small neurons in Huntington dise12
Exophytic cerebellopontine angle tumor showing mostly an embryonal appearance with H3‐3A K27M12
A case of “genetically defined” radiation‐induced glioma: 29 years after surgery and radiation for pilocytic astrocytoma12
Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies9
Erdheim‐Chester disease of brain parenchyma without any systemic involvement: A case report and review of literature9
Concurrent intraventricular intracranial myxoid mesenchymal tumor and ependymoma in a long‐term Ewing sarcoma survivor9
Ependymoma‐like tumor with mesenchymal differentiation (ELTMD) with ZFTA:NCOA1 fusion: A diagnostic challenge9
Simple and clear differentiation of spinocerebellar degenerations: Overview of macroscopic and low‐power view findings8
The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality8
An autopsy case of amyloid angiopathy‐related cerebellar hemorrhage8
Effectiveness of radiation therapy on brain invasion by human papillomavirus‐related multiphenotypic sinonasal carcinoma: A case report8
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Elevated expression of N‐myc downstream regulated gene 1 protein in glioblastomas reflects tumor angiogenesis and poor patient prognosis8
The predominance of “astrocytic” intranuclear inclusions in neuronal intranuclear inclusion disease manifesting encephalopathy‐like symptoms: A case series with brain biopsy7
A comparison of cerebral amyloid angiopathy in the cerebellum and CAA‐positive occipital lobe of 60 brains from routine autopsies7
Unveiling primary intracranial eosinophilic angiocentric fibrosis: A rare case report and diagnostic dilemmas7
Engeletin ameliorates sevoflurane‐induced cognitive impairment by activating PPAR‐gamma in neonatal mice7
Polymerized Type I Collagen With Polyvinylpyrrolidone Reduces Fibrosis and Improves Nerve Organization and Myelination After Peripheral Nerve Injury6
Correction to “Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C > T/p.P307L) in SLC20A2 showing widespread cerebr6
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Blood–brain barrier dysfunction in multiple system atrophy: A human postmortem study6
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Fukutin regulates tau phosphorylation and synaptic function: Novel properties of fukutin in neurons6
Radiologic–pathologic association of tumor‐like lesions with inflammation in cerebral white matter: Comparison of two cases with distinct clinical outcomes5
A case of CIC‐rearranged sarcoma with CIC‐LEUTX gene fusion in spinal cord5
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Balamuthia mandrillarisamoebic encephalitis mimicking tuberculous meningitis5
Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association5
Supratentorial multifocal gliomas associated with Ollier disease harboring IDH1 R132H mutation: A case report5
Neuropilin‐1 enhances temozolomide resistance in glioblastoma via the STAT1/p53/p21 axis5
A case of childhood unilateral relapsing primary angiitis of the central nervous system5
Familial idiopathic basal ganglia calcification with a heterozygous missense variant (c.902C>T/p.P307L) in SLC20A2 showing widespread cerebrovascular lesions5
Possible association of limbic tau pathology with psychosis or behavioral disturbances: Studies of two autopsied psychiatric patients5
Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis5
Malignancy arising in adamantinomatous craniopharyngioma: Report of a rare case with unusual morphologic features5
An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy5
Documented growth of an intracranial capillary hemangioma: A case report5
Senile plaque calcification of the lamina circumvoluta medullaris in Alzheimer's disease5
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NLRP3 inflammasome inhibitor ameliorates ischemic stroke by reprogramming the phenotype of microglia/macrophage in a murine model of distal middle cerebral artery occlusion4
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Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 34
Multiple Neuropathologies Underly Hippocampal Subfield Atrophy in a Case With a Slowly Progressive Amnestic Syndrome: Challenging the Notion of Pure LATENC4
Somatic mosaicism of the PI3K‐AKT‐MTOR pathway is associated with hemimegalencephaly in fetal brains4
Central nervous tissue in ovarian mature teratoma: A neuropathological study of 101 resected tumors4
Primary Rosai‐Dorfman disease of the central nervous system: A clinical, histological, and molecular appraisal4
An autopsy case of adult‐onset neuronal intranuclear inclusion disease with perivascular preservation in cerebral white matter4
MYCN amplification in spinal ependymoma: A five‐year retrospective study4
Japanese Society of Neuropathology Award 20214
FOXM1‐mediated NUF2 expression confers temozolomide resistance to human glioma cells by regulating autophagy via the PI3K/AKT/mTOR signaling path4
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Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?3
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A case of Epstein–Barr virus‐associated smooth muscle tumor of the posterior interosseous nerve mimicking schwannoma3
Calcifying pseudoneoplasms of the neuraxis (CAPNON). A case report3
Tufted astrocyte‐like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?3
Amyotrophic lateral sclerosis with speech apraxia, predominant upper motor neuron signs, and prominent iron accumulation in the frontal operculum and precentral gyrus3
Usefulness of intraoperative rapid immunohistochemistry in the surgical treatment of brain tumors3
A case of intracranial myxoid mesenchymal tumor with EWSR1:CREM fusion in an adult female: Extensive immunohistochemical evaluation3
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A case of myxopapillary ependymoma with predominant giant cell morphology: A rare entity with comprehensive genomic profiling and review of literature3
Gliosarcoma with unusual glial components: Two case reports3
Primary central nervous system extranodal NK/T‐cell lymphoma, nasal type with CD20 expression: Case report and review of the literature3
Corticobasal degeneration with visual hallucination as an initial symptom: A case report3
Alzheimer's Disease With Cardiac Transthyretin Amyloidosis: A Clinicopathological Study of Autopsy Cases3
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Embryonal tumor with multilayered rosettes arising from the internal auditory canal of an adult: Illustrative case with molecular investigations3
Intravascular large B‐cell lymphoma affecting multiple cranial nerves: A histopathological study3
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Clinicopathological heterogeneity of Alzheimer's disease with pure Alzheimer's disease pathology: Cases associated with dementia with Lewy bodies, very early‐onset dementia, and primary progressive ap2
From pathological mechanisms in Krabbe disease to cutting‐edge therapy: A comprehensive review2
Epstein–Barr virus‐positive monoclonal lymphoplasmacytic proliferation associated with neurosyphilis in an immunocompetent patient: A case report2
Japanese Society of Neuropathology Award 20232
An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings2
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Lymphomatosis cerebri with coexistent anti‐N‐methyl‐D‐aspartate receptor antibody: A case report2
Pathology for severe inflammatory PML with PD1/PD‐L1 expression of favorable prognosis: What's a prognostic factor for PML‐IRIS?2
Sebaceous adenoma occurring within an intracranial dermoid cyst2
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosis2
Brain cutting and trimming2
Macroscopic findings of brain with dementia2
White matter edematous change with moderate vascular lesions in pretreated acute stage of leukoencephalopathy with cerebral amyloid angiopathy2
A descriptive study of Parkinson disease and atypical parkinsonisms in the Annuals of the Pathological Autopsy Cases in Japan2
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Glioblastoma and malignant melanoma: Serendipitous or anticipated association?2
An autopsy case of progressive multifocal leukoencephalopathy with massive iron deposition in juxtacortical lesions2
Myopathic changes caused by protein aggregates in adult‐onset spinal muscular atrophy2
Polyglucosan body disease in an aged chimpanzee (Pan troglodytes)2
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Acute respiratory failure caused by brainstem demyelinating lesions in an older patient with an atypical relapsing autoimmune disorder2
Repeated recurrent intracerebral hemorrhage may be involved in cerebral amyloid angiopathy‐related inflammation: An autopsy case2
Pathological features of inflammatory myopathy as a manifestation of chronic graft‐versus‐host disease after allogeneic bone marrow transplantation2
Multisystem pathology in McLeod syndrome2
Diffuse Lewy body disease presenting as Parkinson's disease with progressive aphasia2
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A rare case of dedifferentiated intracranial solitary fibrous tumor with chondrosarcomatous differentiation2
Primary intracranial dedifferentiated liposarcoma: An extremely rare site with unusual histopathological findings2
Usefulness of intraoperative rapid flow cytometry in the surgical treatment of brain tumors2
Clinicopathological features of progressive supranuclear palsy with asymmetrical atrophy of the superior cerebellar peduncle2
Comments on an autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau2
ASK1 activation in glial cells in post‐mortem multiple sclerosis tissue1
Extracranial metastatic solitary fibrous tumor/hemangiopericytoma expressing G‐CSF and its receptor1
Ipsilateral simultaneous multiple hypertensive intracerebral hemorrhages: Analysis of hematoma formation and comparison with distribution of hypertensive mixed‐type hematoma1
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Glioblastoma, IDH‐wildtype manifesting as intracranial hemorrhage: A case report highlighting the clinical utility of digital polymerase chain reaction in integrated diagnoses1
Prednisolone improves hippocampal regeneration after trimethyltin‐induced neurodegeneration in association with prevention of T lymphocyte infiltration1
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Amyotrophic lateral sclerosis with TDP‐43 abnormalities exhibiting globular glial tau inclusions in frontotemporal lobes and pallido‐nigral system1
Extremely rare occurrence of multiple cranial fasciitis: A case report1
An autopsy case of progressive supranuclear palsy with severe corticospinal tract degeneration1
Astrocytes in ischemic stroke: Crosstalk in central nervous system and therapeutic potential1
Calcifying pseudoneoplasm of the neuraxis (CAPNON) associated with neurenteric cyst. An autopsy case showing unusual fatal outcome1
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O6‐methylguanine methyltransferase promoter methylation status of glioblastoma cell line clonal population1
The hot cross bun sign in corticobasal degeneration1
A rare case of primary neuroendocrine carcinoma of the central nervous system1
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Anti‐N‐methyl‐D‐aspartate receptor encephalitis with concurrent human herpes virus‐6A deoxyribonucleic acid detection: An autopsy case1
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MYB::QKI fusion‐positive diffuse glioma of the cerebellum: A case report1
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Let's cluster cases in Neuropathology Case Cluster series!: Unveil clinical masqueraders (Neuropathology Cluster Case 1–13)1
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An autopsy case of amyotrophic lateral sclerosis with striatonigral and pallidoluysian degeneration and cat's‐eye‐shaped neuronal nuclear inclusions1
Intracranial myxoid angiomatoid fibrous histiocytoma with “classic” histology and EWSR1:CREM fusion providing insight for reconciliation with intracranial myxoid mesenchymal tumors1
Rare dual‐genotype IDH mutant glioma: Review of previously reported cases and two new cases of true “oligoastrocytoma”1
Pituitary tuberculoma with panhypopituitarism masquerading as a pituitary adenoma1
Cotton rats (Sigmodon hispidus) with a high prevalence of hydrocephalus without clinical symptoms1
Hereditary spastic paraplegia with thin corpus callosum and SPG11 mutation: A neuropathological evaluation1
A glioneuronal tumor with neurocytic rosettes harboring FGFR1 internal tandem duplication – A report of a unique case1
The Monocarboxylate Transporters MCT1 and MCT4 Are Highly Expressed in Glioblastoma and Crucially Implicated in the Pathobiology1
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Recurrent oligodendroglioma with changed 1p/19q status1
Granular cell tumor of the neurohypophysis presenting as a third ventricle mass1
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An autopsy case of type A FTLD‐TDP with a GRN mutation presenting with the logopenic variant of primary progressive aphasia at onset and with corticobasal syndrome subsequ1
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A DRPLA‐Affected Family: Clinical Course and Autopsy Findings in a Long‐Surviving Case1
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A case of ganglioglioma grade 3 withH3 K27Mmutation arising in the medial temporal lobe in an elderly patient1
Intracranial phosphaturic mesenchymal tumors. A case report and review of literature1
V180I genetic Creutzfeldt‐Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain1
In‐house molecular diagnosis of diffuse glioma updating the revised WHO classification by a platform of the advanced medical care system, Senshin‐Iryo1
Primary degeneration of oculomotor, motor, and somatosensory systems and auditory and visual pathways in spinocerebellar ataxia type 7: A clinicopathological study in a Japanese autopsy case1
Identification and characterization of sex‐dependent gene expression profile in glioblastoma1
Astroblastoma With MN1::BEND2 Fusion Showing an Atypical Signal Pattern in MN1 Break‐Apart FISH: A Potential Diagnostic Pitfall1
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Lactotroph PitNET/adenoma associated to granulomatous hypophysitis in a patient with Crohn's disease: A case report0
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Primary central nervous system other iatrogenic immunodeficiency‐associated lymphoproliferative disorders presenting as extraosseous plasmacytoma with a progressive clinical course: A case report and 0
A case of a pilocytic astrocytoma with histological features of anaplasia and unprecedent genetic alterations0
Primary cauda equina lymphoma confirmed by autopsy: A case report0
Neuropathology Case Cluster: Neuropathology of focal cortical, behavioral, and psychiatric syndromes in neurodegenerative diseases (neuropathology cluster case 14–32)0
The landscape of common genetic drivers and DNA methylation in low‐grade (epilepsy‐associated) neuroepithelial tumors: A review0
Progressive supranuclear palsy with predominant frontal presentation exhibiting progressive nonfluent aphasia due to crossed aphasia0
Motor involvement in frontotemporal lobar degeneration with TAR DNA‐binding protein of 43 kDa type C0
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Neuropil‐like islands are a possible pathogenetic link between glioblastoma and gangliocytoma/ganglioglioma in a case of synchronous bilateral brain tumors0
Unprecedented Combination of Rare Degenerative Pathologies in an Octogenarian Ex‐Football Player0
Utilizing quantitative susceptibility mapping to differentiate primary lateral sclerosis from progressive supranuclear palsy: A case report0
A case of cerebral paragonimiasis misdiagnosed as eosinophilic granulomatosis with polyangiitis0
The receptor for advanced glycation end products and its ligands’ expression in OVE26 diabetic sciatic nerve during the development of length‐dependent neuropathy0
Retrospective neuropathological diagnosis of TDP‐43 proteinopathies: Factors affecting immunoreactivity of phosphorylated TDP‐43 in fixed post‐mortem brain tissue0
An EWSR1–EZHIP fusion in a cerebral hemisphere astroblastoma0
Cervical myelopathy and extensive body destruction caused by primary Gli1 fusion sarcoma0
Artificial intelligence techniques for neuropathological diagnostics and research0
Intraventricular mucin‐producing glioblastoma arising in the septum pellucidum at the frontal horn of the lateral ventricle: A case report0
Systemic inflammation caused by an intracranial mesenchymal tumor with a EWSR1::CREM fusion presenting associated with IL‐6/STAT3 signaling0
Embryonal tumor with multilayered rosettes, DICER1‐mutated, showing histologically unique neuronal differentiation after chemoradiotherapy0
Clinicopathological diversity of semantic dementia: Comparisons of patients with early‐onset versus late‐onset, left‐sided versus right‐sided temporal atrophy, and TDP‐type A versus type C pathology0
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Spinal muscular atrophy type 2 patient who survived 61 years: an autopsy case report0
Pediatric fibromyxoid tumor with PLAG1 fusion: An emerging entity with a novel intracranial location0
Solitary fibrous tumor of the central nervous system with epithelioid neuroendocrine “Transdedifferentiation”: A case report and review of the literatures0
An autopsy case of Alzheimer's disease with amygdala‐predominant Lewy pathology presenting with frontotemporal dementia‐like psychiatric symptoms0
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Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy0
Implications for soluble iron accumulation, oxidative stress, and glial glutamate release in motor neuron death associated with sporadic amyotrophic lateral sclerosis0
Expression and distribution of hypoxia‐inducible factor‐1α and vascular endothelial growth factor in comparison between radiation necrosis and tumor tissue in metastatic brain tumor: A case report0
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Expanded ischemic lesion due to herniation leads to axonal injury in a site remote to the primary lesion on autopsy brain with acute focal cerebral ischemia0
An autopsy case of progressive supranuclear palsy treated with monoclonal antibody against tau0
Spinal astroblastoma, MN1 altered in 3‐year‐old child: An uncommon tumor at an unusual site0
Selective extension of cerebral vascular calcification in an autopsy case of Fahr's syndrome associated with asymptomatic hypoparathyroidism0
Some comments on the morphometry of choroid plexus in neurodegenerative diseases0
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Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation0
Immunohistochemical expression of osteopontin and collagens in choroid plexus of human brains0
Spread of vimentin‐immunoreactive cells within the plaque‐like lesion in the spinal anterior horn of a patient with post‐poliomyelitis syndrome0
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Morphometry of choroid plexus epithelial cells in neurodegenerative diseases0
Tumefactive eosinophil‐rich non‐granulomatous small vessel vasculitis in the cerebrum in a patient with idiopathic hypereosinophilic syndrome0
An autopsy case of granulomatous amebic encephalitis caused by Balamuthia mandrillaris involving prior amebic dermatitis0
Nonneoplastic and noninfective cysts of the central nervous system: A histopathological study0
Solitary subependymal giant cell astrocytoma lacking TSC1/2 mutations and TTF‐1 expression: A potential diagnostic pitfall0
Increase in cathepsin K gene expression in Duchenne muscular dystrophy skeletal muscle0
Whorling‐sclerosing meningioma invading skull bone and subcutaneous tissue with an incidental toxoplasmosis: A case report0
IgG4‐related brain pseudotumor mimicking CNS lymphoma. A case report0
Unique Lewy pathology in myotonic dystrophy type 10
Bridging minds: Participant perspectives on postmortem brain research and engagement0
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Association between hypothalamic Alzheimer's disease pathology and body mass index: The Hisayama study0
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Morphological study of the phrenic nerve to determine a reference value for the myelinated fiber density in elderly individuals0
Melanotic pilocytic astrocytoma0
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Intracellular and Extracellular Localization of Transthyretin and Its Association With Amyloid‐β in Alzheimer's Disease Brains0
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Giant cell glioblastoma with lipogenic differentiation in a patient with neurofibromatosis type 1: A case report0
An autopsy case of variably protease‐sensitive prionopathy with Met/Met homogeneity at codon 1290
A rare encounter: Comprehensive case review of myxoid meningiomas with a representative case0
Distribution of amyloid‐β precursor protein‐immunoreactive axons differs according to the severity of cerebral ischemia in autopsy brains0
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The list of reviewers for neuropathology other than editorial board members from October 2023 to September 20240
Microscopical anatomy of the peripheral nervous system: An essential notion for understanding the pathophysiology of very early classic Guillain‐Barré syndrome0
Non‐Neoplastic Lesions of the Ependyma: A Neuropathological Overview0
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A pathologically confirmed case of combined amyotrophic lateral sclerosis with C9orf72 mutation and multiple system atrophy0
Pathological study of progressive supranuclear palsy the cases with mutations in Bassoon0
Numerous spindle‐shaped lymphoma cells in lymphomatosis cerebri: An autopsy case report0
Ependymosarcoma harboring C11orf95:RELA fusion transcript: Report of two cases and review of the literature0
Adenoid glioblastoma: Stromal hypovascularity and secretion of chondromodulin‐I by tumor cells0
Elucidating the multiple genetic alterations involved in the malignant transformation of a KRAS mutant neurenteric cyst. A case report0
Case Report and Literature Review: Overexpression of HMGA in Concomitant Plurihormonal Tumor and Papillary Thyroid Carcinoma0
Japanese Society of Neuropathology Award 20240
Low‐grade B‐cell lymphoma of the central nervous system with plasmacytic differentiation and amyloid deposition0
Integrated assessment of malignancy in IDH‐mutant astrocytoma with p16 and methylthioadenosine phosphorylase immunohistochemistry0
Brain parenchymal angiomatoid fibrous histiocytoma and spinal myxoid mesenchymal tumor with FET: CREB fusion, a spectrum of the same tumor type0
“Burnt‐out” progressive multifocal leukoencephalopathy in idiopathic CD4+ lymphocytopenia0
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Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa0
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