Dural angioleiomyoma of the middle cranial fossa: a case report and review of the literature.

Abstract:

:We describe a case of dural angioleiomyoma (ALM) of the middle cranial fossa. A 62-year-old man was referred to our center for fracture of the left clavicle because of a fall, and he had a sudden seizure during admission. The mass was completely resected. The tumor base was located at the bottom of the temporal lobe in the front of the petrous apex and near the cavernous sinus. After 7 months, the postoperative course demonstrated no tumor recurrence. The lesion had the typical appearance of ALM. Mitoses and necrosis were not identified. The lesion contained multifocality of fat in some areas of spindle-shaped cells, and markedly myxoid change was present. The spindle cells were positive for SMA and DES and negative for EMA, HMB-45, p53 and p16. A small focus of fat was positive for S-100. Less than 1% of the tumor cells showed immunoreactivity for Ki-67. EBV-encoded RNA was negative for tumor cells. Stainings for p53, p16, Ki-67 and EBV infection need to be carried out in cases of intracranial ALM because they are correlated with the biological behavior and prognosis of the tumor.

journal_name

Brain Tumor Pathol

journal_title

Brain tumor pathology

authors

Zhou Z,Yu M,Yang S,Zhou J,Sun R,Yang G

doi

10.1007/s10014-012-0115-z

subject

Has Abstract

pub_date

2013-04-01 00:00:00

pages

117-21

issue

2

eissn

1433-7398

issn

1861-387X

journal_volume

30

pub_type

杂志文章,评审
  • Genetic aberrations and molecular biology of skull base chordoma and chondrosarcoma.

    abstract::Chordomas and chondrosarcomas are two major malignant bone neoplasms located at the skull base. These tumors are rarely metastatic, but can be locally invasive and resistant to conventional chemotherapies and radiotherapies. Accordingly, therapeutic approaches for the treatment of these tumors can be difficult. Additi...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章,评审

    doi:10.1007/s10014-017-0283-y

    authors: Kitamura Y,Sasaki H,Yoshida K

    更新日期:2017-04-01 00:00:00

  • Quantitative digital assessment of MGMT immunohistochemical expression in glioblastoma tissue.

    abstract::Recent reports have suggested an important clinical role for hypermethylation of the O(6)-methylguanine-DNA-methyltransferase (MGMT) promoter in patients with glioblastomas. Whether MGMT protein expression is correlated with promoter hypermethylation and patient outcomes, however, has not been elucidated. Here we desc...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-010-0004-2

    authors: Araki Y,Mizoguchi M,Yoshimoto K,Shono T,Amano T,Nakamizo A,Suzuki SO,Iwaki T,Sasaki T

    更新日期:2011-02-01 00:00:00

  • Prevalence of NRAS, PTEN and AKT1 gene mutations in the central nervous system metastases of non-small cell lung cancer.

    abstract::Somatic mutations in NRAS, PTEN and AKT1 genes are rarely (~1%) reported in primary NSCLC, but their role in carcinogenesis have been proven. Therefore, we assessed the frequency of them in 145 FFPE tissue samples from CNS metastases of NSCLC using the real-time PCR technique. We identified four (two NRAS and single A...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-016-0276-2

    authors: Nicoś M,Krawczyk P,Jarosz B,Sawicki M,Trojanowski T,Milanowski J

    更新日期:2017-01-01 00:00:00

  • Primary central nervous system large B-cell lymphoma with prolific, mixed T-cell and macrophage infiltrates, mimicking multiple sclerosis.

    abstract::Although tissue confirmation is essential for a diagnosis of primary central nervous system large B-cell lymphoma (PCNSBL), accurate assessment may still be difficult, even when tissue is obtained. We report a 59-year-old man, first diagnosed as multiple sclerosis by open biopsy at another institution, who was then co...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-010-0264-x

    authors: Utsuki S,Oka H,Miyazaki T,Yamazaki T,Yasui Y,Fujii K,Kawano N,Tokuyama W,Iwabuchi K,Okayasu I,Yagishita S

    更新日期:2010-04-01 00:00:00

  • Clinicopathological differences between variants of the NAB2-STAT6 fusion gene in solitary fibrous tumors of the meninges and extra-central nervous system.

    abstract::Investigations on the NAB2-STAT6 fusion gene in solitary fibrous tumors (SFTs) and hemangiopericytomas (HPCs) have increased since its discovery in 2013. Although several SFTs reported without NAB2-STAT6 fusion gene analysis, we reviewed 546 SFTs/HPCs with NAB2-STAT6 fusion gene analysis in this study and investigated...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-016-0264-6

    authors: Nakada S,Minato H,Nojima T

    更新日期:2016-07-01 00:00:00

  • Messenger RNA fingerprinting analysis using arbitrarily primed PCR (RAP) of genes expressed during rat C6 glioma cell differentiation.

    abstract::To identify differentially expressed genes involved in rat C6 glioma cell differentiation induced by cyclic AMP, we adopted mRNA fingerprinting using arbitrarily primed polymerase chain reaction (PCR) (RAP). Four complementary DNA (cDNA) fragments differentially expressed during differentiation were isolated, and they...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/BF02478880

    authors: Sakai H,Nakashima S,Nakatani K,Yoshimura S,Nishimura Y,Sakai N,Nozawa Y

    更新日期:1997-01-01 00:00:00

  • Immunohistochemical ATRX expression is not a surrogate for 1p19q codeletion.

    abstract::The IDH-mutant and 1p/19q co-deletion (1p19q codel) provides significant diagnostic and prognostic value in lower-grade gliomas. As ATRX mutation and 1p19q codel are mutually exclusive, ATRX immunohistochemistry (IHC) may substitute for 1p19q codel, but this has not been comprehensively examined. In the current study,...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-018-0312-5

    authors: Yamamichi A,Ohka F,Aoki K,Suzuki H,Kato A,Hirano M,Motomura K,Tanahashi K,Chalise L,Maeda S,Wakabayashi T,Kato Y,Natsume A

    更新日期:2018-04-01 00:00:00

  • Epithelioid glioblastoma: a case report.

    abstract::A 43-year-old woman who had undergone breast cancer surgery 1 year previously complained of headache and nausea. Her brain computed tomography (CT) scan and magnetic resonance imaging (MRI) showed a well-circumscribed, heterogeneously enhanced tumor in the right thalamus. She underwent gross total resection of the tum...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-005-0173-6

    authors: Akimoto J,Namatame H,Haraoka J,Kudo M

    更新日期:2005-01-01 00:00:00

  • Granulofilamentous meningioma.

    abstract::A 55-year old female was referred to the Department of Neurosurgery, Kitasato Hospital, because of a hearing impairment. Neuroimaging revealed a typical meningioma attached to the falx in the right frontal region. During surgery, an encapsulated, circumscribed, reddish-gray, slightly hard tumor attached to the falx wa...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-012-0091-3

    authors: Miyajima Y,Oka H,Utsuki S,Hagiwara H,Inukai M,Kijima C,Hara A,Yasui Y,Kawano N,Fujii K

    更新日期:2013-01-01 00:00:00

  • Rapid immunocytochemistry based on alternating current electric field using squash smear preparation of central nervous system tumors.

    abstract::The role of intraoperative pathological diagnosis for central nervous system (CNS) tumors is crucial for neurosurgery when determining the surgical procedure. Especially, treatment of carmustine (BCNU) wafers requires a conclusive diagnosis of high-grade glioma proven by intraoperative diagnosis. Recently, we demonstr...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-015-0238-0

    authors: Moriya J,Tanino MA,Takenami T,Endoh T,Urushido M,Kato Y,Wang L,Kimura T,Tsuda M,Nishihara H,Tanaka S,R-IHC Study Group.

    更新日期:2016-01-01 00:00:00

  • A case of anaplastic pleomorphic xanthoastrocytoma presenting with tumor bleeding and cerebrospinal fluid dissemination.

    abstract::Pleomorphic xanthoastrocytoma (PXA) has been considered an astrocytic tumor with a relatively favorable prognosis. However, PXA cases having several recurrent patterns with poor prognosis have been reported in recent years, and a new concept of anaplastic PXA has been proposed. The present case was a 59-year-old woman...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-006-0197-6

    authors: Asano K,Miyamoto S,Kubo O,Kikkukawa T,Yagihashi A,Ohkuma H

    更新日期:2006-04-01 00:00:00

  • Clinicopathological characteristics of circumscribed high-grade astrocytomas with an unusual combination of BRAF V600E, ATRX, and CDKN2A/B alternations.

    abstract::We report four cases of high-grade astrocytoma with a BRAF V600E mutation, ATRX inactivation, and CDKN2A/B homozygous deletion. Children to young adults aged 3-46 presented with a well demarcated contrast-enhancing mass in the supratentorial area. Pathological examination revealed packed growth of short spindle to rou...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-019-00344-z

    authors: Murakami C,Yoshida Y,Yamazaki T,Yamazaki A,Nakata S,Hokama Y,Ishiuchi S,Akimoto J,Shishido-Hara Y,Yoshimoto Y,Matsumura N,Nobusawa S,Ikota H,Yokoo H

    更新日期:2019-07-01 00:00:00

  • Next-generation whole exome sequencing of glioblastoma with a primitive neuronal component.

    abstract::Glioblastoma with a primitive neuronal component (GBM-PN) was renamed from glioblastoma with primitive neuroectodermal tumor-like component (GBM-PNET) in the new WHO classification of tumors of the central nervous system in 2016. GBM-PN is a rare variant of glioblastoma. There were not so many publications on the inve...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-019-00334-1

    authors: Xu G,Zheng H,Li JY

    更新日期:2019-07-01 00:00:00

  • Expression of the multidrug-resistance P-glycoprotein (Pgp, MDR-1) by endothelial cells of the neovasculature in central nervous system tumors.

    abstract::To elucidate the expression of the MDR1 gene products P-glycoprotein (Pgp) in endothelial cells of newly formed blood microvessels in brain tumors, 30 brain tumors were examined by immunohistochemistry using an anti-Pgp monoclonal antibody, JSB-1. Positive reactions for JSB-1 were detected in endothelial cells in newl...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/BF02478898

    authors: Sawada T,Kato Y,Sakayori N,Takekawa Y,Kobayashi M

    更新日期:1999-01-01 00:00:00

  • Pineal parenchymal tumor with marked retinoblastic differentiation: case report.

    abstract::A 53-year-old woman was found to have a tumor in the pineal region. Histologically, Homer-Wright rosettes were sporadically distributed in a diffuse proliferation of round tumor cells that were immunoreactive for synaptophysin and chromogranin. A few perivascular pseudorosettes were also present, and the perivascular ...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/BF02478945

    authors: Utsuki S,Kawano N,Oka H,Fukushima Y,Kondo K,Tanizaki Y,Yashui Y,Fujii K,Yagishita S

    更新日期:2003-01-01 00:00:00

  • Molecular profiling of different glioma specimens from an Ollier disease patient suggests a multifocal disease process in the setting of IDH mosaicism.

    abstract::Ollier disease (OD) and Maffucci syndrome are rare conditions due to a post-zygotic somatic mutation that results in mosaicism. In addition to enchondromas and hemangiomas, some of these patients also develop other unrelated tumors, such as gliomas, that harbor IDH mutations, suggesting that an IDH mutation is a commo...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章,评审

    doi:10.1007/s10014-018-0327-y

    authors: Tan CL,Vellayappan B,Wu B,Yeo TT,McLendon RE

    更新日期:2018-10-01 00:00:00

  • Genetic landscape of meningioma.

    abstract::Meningioma is the most common intracranial tumor, arising from arachnoid cells of the meninges. Monosomy 22 and inactivating mutations of NF2 are well-known genetic alterations of meningiomas. More recently, mutations in TRAF7, AKT1, KLF4, SMO, and PIK3CA were identified by next-generation sequencing. We here reviewed...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章,评审

    doi:10.1007/s10014-016-0271-7

    authors: Yuzawa S,Nishihara H,Tanaka S

    更新日期:2016-10-01 00:00:00

  • The density of microvessels positive for Wilms' tumour-1 protein (WT-1) is an independent predictor of recurrence risk in meningiomas.

    abstract::Wilms' tumour-1 (WT-1) protein m-RNA was recently demonstrated in meningiomas, suggesting the potential application of WT-1 immunotherapy in these tumours. The aim of the present study was to analyze the immunohistochemical expression of WT-1 protein, its correlation with the clinico-pathological variables and associa...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-015-0217-5

    authors: Barresi V,Caffo M,Branca G,Vitarelli E,Tuccari G

    更新日期:2015-07-01 00:00:00

  • Prognostic role of H3K27M mutation, histone H3K27 methylation status, and EZH2 expression in diffuse spinal cord gliomas.

    abstract::The objective of this study is to clarify clinical significance of the H3F3A K27M mutation (H3K27M) and analyze the correlation between H3K27M, H3K27me3 status, and EZH2 expression and prognosis in spinal cord gliomas. Patients with spinal cord diffuse glioma regardless of World Health Organization (WHO) grade underwe...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-020-00369-9

    authors: Ishi Y,Takamiya S,Seki T,Yamazaki K,Hida K,Hatanaka KC,Ishida Y,Oda Y,Tanaka S,Yamaguchi S

    更新日期:2020-07-01 00:00:00

  • High expression of L-type amino acid transporter 1 in infiltrating glioma cells.

    abstract::L-type amino acid transporter 1 (LAT1), a neutral amino acid transport agent, is essential for the transport of large neutral amino acids. LAT1 also corresponds to tumor-associated gene-1 (TA1), an oncofetal antigen that is expressed primarily in fetal tissues and cancer cells such as glioma cells. We have investigate...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-005-0188-z

    authors: Nawashiro H,Otani N,Uozumi Y,Ooigawa H,Toyooka T,Suzuki T,Katoh H,Tsuzuki N,Ohnuki A,Shima K,Shinomiya N,Matsuo H,Kanai Y

    更新日期:2005-01-01 00:00:00

  • Clinicopathological features of sellar region xanthogranuloma: correlation with Rathke's cleft cyst.

    abstract::Xanthogranuloma of the sellar region is a rare clinical observation. Although it was included in the World Health Organization (WHO) brain tumor classification in 2000, its clinical features and pathogenesis remain uncertain. We report herein seven cases of xanthogranuloma of the sellar region who underwent transsphen...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-012-0130-0

    authors: Amano K,Kubo O,Komori T,Tanaka M,Kawamata T,Hori T,Okada Y

    更新日期:2013-10-01 00:00:00

  • Expression and quantitative analysis of matrix metalloproteinase-2 and -9 in human gliomas.

    abstract::The matrix metalloproteinase (MMP) family members catalyze extracellular proteolysis. Recent reports have suggested that expression of MMP-2 and -9 might play a critical role in neoplastic tissue invasion or metastasis. In this study, the relationship between the expression of MMP-2 and -9 and the histological feature...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/BF02482184

    authors: Komatsu K,Nakanishi Y,Nemoto N,Hori T,Sawada T,Kobayashi M

    更新日期:2004-01-01 00:00:00

  • ATRX status correlates with 11 C-methionine uptake in WHO grade II and III gliomas with IDH1 mutations.

    abstract::Recent studies on gliomas have shown frequent alterations in the alpha-thalassemia/mental retardation syndrome X-linked gene (ATRX). This study was designed to determine whether ATRX status correlates with uptake of 11C-methionine in WHO grades II and III gliomas. Sixty-two patients underwent 11C-methionine positron e...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-017-0280-1

    authors: Ogishima T,Tamura K,Kobayashi D,Inaji M,Hayashi S,Tamura R,Nariai T,Ishii K,Maehara T

    更新日期:2017-01-01 00:00:00

  • A case of isolated langerhans cell histiocytosis of the hypothalamus with remission and regrowth after surgery.

    abstract::We describe a new case of isolated Langerhans cell histiocytosis (LCH) of the hypothalamus. A 53-year-old female patient presented with polydipsia, headache, anorexia, and fatigue. Neurological imaging revealed a mass projecting from the hypothalamus into the third ventricle. Gross total removal of the tumor was perfo...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/BF02484517

    authors: Horiguchi K,Fujii T,Nakazato Y

    更新日期:2004-01-01 00:00:00

  • Evaluation of sensitivity and specificity of doublecortin immunostatining for the detection of infiltrating glioma cells.

    abstract::Diffuse gliomas are highly infiltrative intracranial tumors, but there are few useful markers for detecting infiltrating glioma cells in the surrounding brain tissue. Doublecortin (DCX) is a microtubule-associated protein (MAP) that plays a crucial role in neuroblast migration. It was recently demonstrated that DCX is...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-007-0225-1

    authors: Masui K,Mawatari SY,Suzuki SO,Iwaki T

    更新日期:2008-01-01 00:00:00

  • Primary malignant lymphoma of the brain: analysis of MMAC1 (PTEN) tumor suppressor gene.

    abstract::With the use of RT-PCR (reverse transcriptase-polymerase chain reaction), Northern blot analysis, and Western blot analysis, seven primary brain lymphomas were examined for the state of the MMACI tumor suppressor gene. Nucleotide analysis of RT-PCR clones revealed no abnormality in the MMAC1 coding sequence in each ca...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/BF02479427

    authors: Ding X,Endo S,Zhang SJ,Saito T,Kouno M,Kuroiwa T,Washiyama K,Kumanishi T

    更新日期:2001-01-01 00:00:00

  • Primary central nervous system lymphoma in acquired immune deficiency syndrome mimicking toxoplasmosis.

    abstract::A 37-year-old man, a hepatitis B virus carrier due to mother-to-child transmission, had a medical examination in September 2008 in nearby hospitals due to anorexia and weight loss. He was transported to our hospital because computed tomography (CT) detected intracranial lesions, and he had a positive human immunodefic...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-010-0001-5

    authors: Utsuki S,Oka H,Abe K,Osawa S,Yamazaki T,Yasui Y,Fujii K

    更新日期:2011-02-01 00:00:00

  • Detection of failure of bevacizumab treatment for malignant glioma based on urinary matrix metalloproteinase activity.

    abstract::Although antiangiogenic treatment for malignant glioma using bevacizumab in combination with irinotecan chemotherapy has a promising effect on survival, the high incidence of increasing infiltrative tumors can be a problem in resistance to antiangiogenic therapy. In this study, we detected failure of bevacizumab treat...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-010-0271-y

    authors: Takano S,Mashiko R,Osuka S,Ishikawa E,Ohneda O,Matsumura A

    更新日期:2010-10-01 00:00:00

  • Clinicopathological features from long-term observation of a papillary tumor of the pineal region (PTPR): a case report.

    abstract::Papillary tumor of the pineal region (PTPR) was recently added to the 2007 WHO classification of tumors of the central nervous system as a rare pineal tumor. We present a case of a 17-year-old man who developed a 3-cm pineal tumor that was incompletely excised following two operations. The pathological findings presen...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章

    doi:10.1007/s10014-009-0246-z

    authors: Yano H,Ohe N,Nakayama N,Shinoda J,Iwama T

    更新日期:2009-01-01 00:00:00

  • Glioma-initiating cells and molecular pathology: implications for therapy.

    abstract::There is now compelling evidence that gliomas harbor a small population of cells, termed glioma-initiating cells (GICs), characterized by their ability to undergo self-renewal and initiate tumorigenesis. The development of therapeutic strategies targeted toward GIC signaling may improve the treatment of malignant glio...

    journal_title:Brain tumor pathology

    pub_type: 杂志文章,评审

    doi:10.1007/s10014-010-0011-3

    authors: Natsume A,Kinjo S,Yuki K,Kato T,Ohno M,Motomura K,Iwami K,Wakabayashi T

    更新日期:2011-02-01 00:00:00