Database : MEDLINE
Search on : Pinealoma [Words]
References found : 1638 [refine]
Displaying: 1 .. 10   in format [Detailed]

page 1 of 164 go to page                         

  1 / 1638 MEDLINE  
              next record last record
select
to print
Photocopy
Full text

[PMID]: 28960912
[Au] Autor:van Engelen K; Villani A; Wasserman JD; Aronoff L; Greer MC; Tijerin Bueno M; Gallinger B; Kim RH; Grant R; Meyn MS; Malkin D; Druker H
[Ad] Address:Genetics and Genome Biology Program, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
[Ti] Title:DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center.
[So] Source:Pediatr Blood Cancer;65(1), 2018 Jan.
[Is] ISSN:1545-5017
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:BACKGROUND: To expand the current knowledge of DICER1 syndrome and to propose criteria for genetic testing based on experience at a pediatric tertiary care center. PROCEDURE: This study involved a retrospective chart review of the 78 patients (47 probands and 31 family members) seen in the Cancer Genetics Program at The Hospital for Sick Children (SickKids) who were offered genetic testing for DICER1. RESULTS: Of 47 probands offered genetic testing for DICER1, 46 pursued testing: 11 (23.9%) carried a pathogenic variant and one proband (2.1%) carried a missense variant of uncertain significance with evidence for pathogenicity. Thirty-one family members of variant-positive probands were offered testing: eight of the 25 who agreed to testing carried their familial variant (32.0%). Overall, 20 patients were identified to have a variant in DICER1 (eight males, 12 females). Of these, 13 (65.0%) presented with clinical manifestations associated with the syndrome. The most common lesions were pleuropulmonary blastoma (PPB) (five of 20 patients, 25.0%) and pineoblastoma (three of 20 patients, 15.0%). The average age at which individuals were diagnosed with a primary neoplasm was 5.2 years (range 0.8-20 years, median 3.0). Surveillance at our institution, with a median follow-up time of 23 months, has identified PPB in two asymptomatic individuals. These lesions were identified at early stages, thus potentially reducing treatment-related morbidity and mortality. CONCLUSION: This study further delineates the DICER1 syndrome phenotype and demonstrates the feasibility of a DICER1 syndrome surveillance protocol for the early detection of tumors.
[Mh] MeSH terms primary: Brain Neoplasms/genetics
Neoplastic Syndromes, Hereditary/genetics
Pineal Gland
Pinealoma/genetics
Pulmonary Blastoma/genetics
[Mh] MeSH terms secundary: Adolescent
Adult
Brain Neoplasms/metabolism
Brain Neoplasms/pathology
Child
Child, Preschool
Female
Follow-Up Studies
Humans
Infant
Infant, Newborn
Male
Neoplastic Syndromes, Hereditary/mortality
Neoplastic Syndromes, Hereditary/pathology
Pinealoma/mortality
Pinealoma/pathology
Pulmonary Blastoma/mortality
Pulmonary Blastoma/pathology
[Pt] Publication type:CLINICAL TRIAL; JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171201
[Lr] Last revision date:171201
[Js] Journal subset:IM
[Da] Date of entry for processing:170930
[St] Status:MEDLINE
[do] DOI:10.1002/pbc.26720

  2 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 29057188
[Au] Autor:Naqvi S; Rupareliya C; Shams A; Hameed M; Mahuwala Z; Giyanwani PR
[Ad] Address:Jinnah Postgraduate Medical Centre, Jinnah Sindh Medical University (SMC).
[Ti] Title:Pineal Gland Tumor but not Pinealoma: A Case Report.
[So] Source:Cureus;9(8):e1576, 2017 Aug 18.
[Is] ISSN:2168-8184
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:The pineal gland is a small pinecone-shaped and functionally endocrine structure located in the epithalamus region. Developmentally, the pineal gland is considered as a part of the epithalamus. It plays a role in the entrainment of the circadian rhythms of an organism by producing melatonin, a functionally important hormone. Lesions of the pineal region are rare compared to other parts of the brain. A lesion may be tumorous or non-tumorous in nature. The most common lesions are tumors that are pineal parenchymal tumors (PPT) in origin. Gliomas are the second most common tumors in the pineal region. We report a case of a high-grade oligodendroglioma, not commonly seen in the pineal region, in a 45-year-old male. The patient was suspected to have a mass in the pineal region on a computed tomography (CT) scan and histology confirmed the diagnosis of oligodendroglioma. This is a unique case because only five such cases have been reported so far.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1710
[Cu] Class update date: 171025
[Lr] Last revision date:171025
[St] Status:PubMed-not-MEDLINE
[do] DOI:10.7759/cureus.1576

  3 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28777035
[Au] Autor:Roland JL; Price RL; Kamath AA; Akbari SH; Leuthardt EC; Miller BA; Smyth MD
[Ad] Address:Departments of 1 Neurological Surgery.
[Ti] Title:Hydrocephalus presenting as idiopathic aqueductal stenosis with subsequent development of obstructive tumor: report of 2 cases demonstrating the importance of serial imaging.
[So] Source:J Neurosurg Pediatr;20(4):329-333, 2017 Oct.
[Is] ISSN:1933-0715
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:The authors describe 2 cases of triventricular hydrocephalus initially presenting as aqueductal stenosis that subsequently developed tumors of the pineal and tectal region. The first case resembled late-onset idiopathic aqueductal stenosis on serial imaging. Subsequent imaging revealed a new tumor in the pineal region causing mass effect on the midbrain. The second case presented in a more typical pattern of aqueductal stenosis during infancy. On delayed follow-up imaging, an enlarging tectal mass was discovered. In both cases hydrocephalus was successfully treated by cerebrospinal fluid diversion prior to tumor presentation. The differential diagnoses, diagnostic testing, and treatment course for these unusual cases are discussed. The importance of follow-up MRI in cases of idiopathic aqueductal stenosis is emphasized by these exemplar cases.
[Mh] MeSH terms primary: Brain Neoplasms/etiology
Hydrocephalus/complications
Hydrocephalus/surgery
Pineal Gland/pathology
Third Ventricle/surgery
Ventriculostomy/methods
[Mh] MeSH terms secundary: Child
Disease Progression
Female
Follow-Up Studies
Humans
Hydrocephalus/diagnostic imaging
Infant
Magnetic Resonance Imaging
Male
Pineal Gland/diagnostic imaging
Pinealoma/diagnostic imaging
Pinealoma/etiology
Tectum Mesencephali/diagnostic imaging
Tectum Mesencephali/pathology
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1710
[Cu] Class update date: 171006
[Lr] Last revision date:171006
[Js] Journal subset:IM
[Da] Date of entry for processing:170805
[St] Status:MEDLINE
[do] DOI:10.3171/2017.5.PEDS1779

  4 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28719464
[Au] Autor:Coy S; Dubuc AM; Dahiya S; Ligon KL; Vasiljevic A; Santagata S
[Ad] Address:*Department of Pathology, Brigham and Women's Hospital, Harvard Medical School ‡Department of Pathology, Boston Children's Hospital, Harvard Medical School Departments of §Medical Oncology ¶Cancer Biology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA †Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO ∥East Pathology and Neuropathology Center, East Hospital Group, University Hospital of Lyon Bron, France.
[Ti] Title:Nuclear CRX and FOXJ1 Expression Differentiates Non-Germ Cell Pineal Region Tumors and Supports the Ependymal Differentiation of Papillary Tumor of the Pineal Region.
[So] Source:Am J Surg Pathol;41(10):1410-1421, 2017 Oct.
[Is] ISSN:1532-0979
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Papillary tumor of the pineal region (PTPR) is a neuroepithelial neoplasm first described in 2003. Despite the anatomic association of PTPR with the pineal gland, the features of these tumors resemble those of the ependymal circumventricular subcommissural organ (SCO) of the posterior third ventricle. Given the presumed distinct derivation of PTPR and pineal parenchymal tumors, we hypothesized that expression of lineage-specific transcription factors could distinguish these tumors and provide additional insight into the differentiation of PTPR. A broad series of pineal region samples was reviewed, including 7 benign pineal glands, 4 pineal cysts, 13 pineocytomas, 28 pineal parenchymal tumors of intermediate differentiation, 11 pineoblastomas, and 18 PTPR. All samples were evaluated by immunohistochemistry for expression of CRX, a master transcriptional regulator of photoreceptor differentiation expressed in pineal gland and retina and/or FOXJ1, a master transcriptional regulator of ciliogenesis expressed in normal ependymal cells and ependymal neoplasms. Diffuse nuclear CRX expression is present in 100% of pineal samples. FOXJ1 is negative in all pineal samples. CRX staining is present in 53% of PTPR, though expression is nearly always limited to rare cells. Diffuse nuclear FOXJ1 expression is present in 100% of PTPR. Fetal human SCO diffusely expressed FOXJ1 but was negative for CRX. Immunohistochemistry for FOXJ1 and CRX differentiates non-germ cell pineal region tumors with high sensitivity and specificity, including pineal parenchymal tumors and PTPR. Our findings support the hypothesis that PTPR have ependymal differentiation and are phenotypically more similar to SCO than pineal gland.
[Mh] MeSH terms primary: Brain Neoplasms/pathology
Forkhead Transcription Factors
Homeodomain Proteins
Pineal Gland
Pinealoma/pathology
Trans-Activators
[Mh] MeSH terms secundary: Brain Neoplasms/chemistry
Brain Neoplasms/metabolism
Cell Differentiation
Cell Nucleus/metabolism
Forkhead Transcription Factors/analysis
Forkhead Transcription Factors/biosynthesis
Homeodomain Proteins/analysis
Homeodomain Proteins/biosynthesis
Humans
Pinealoma/chemistry
Pinealoma/metabolism
Trans-Activators/analysis
Trans-Activators/biosynthesis
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (FOXJ1 protein, human); 0 (Forkhead Transcription Factors); 0 (Homeodomain Proteins); 0 (Trans-Activators); 0 (cone rod homeobox protein)
[Em] Entry month:1710
[Cu] Class update date: 171002
[Lr] Last revision date:171002
[Js] Journal subset:IM
[Da] Date of entry for processing:170719
[St] Status:MEDLINE
[do] DOI:10.1097/PAS.0000000000000903

  5 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28602925
[Au] Autor:Choque-Velasquez J; Colasanti R; Resendiz-Nieves JC; Jahromi BR; Kozyrev DA; Thiarawat P; Hernesniemi J
[Ad] Address:Department of Neurosurgery, Helsinki University Hospital, Helsinki, Finland. Electronic address: johchove@hotmail.com.
[Ti] Title:Supracerebellar Infratentorial Paramedian Approach in Helsinki Neurosurgery: Cornerstones of a Safe and Effective Route to the Pineal Region.
[So] Source:World Neurosurg;105:534-542, 2017 Sep.
[Is] ISSN:1878-8769
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:OBJECTIVE: The supracerebellar infratentorial (SCIT) paramedian approach in sitting position represents one of the most used surgical routes for dealing with pineal region lesions. The purpose of this study is to determine the cornerstones to perform this approach in a simple, safe, and effective way, so that it could be easily reproduced in other neurosurgical centers, particularly in those with modest resources. METHODS: We reviewed and analyzed the surgical videos of 24 pineal region lesions that were operated on through an SCIT approach between June 2012 and October 2015. The SCIT approach may be divided into 3 main steps: 1) skin-muscle incision; 2) craniotomy; and 3) dura opening and access to the pineal region. RESULTS: Complete lesion removal was accomplished in 23 cases, and subtotal removal was accomplished in 1 case. The pineal region was effectively and safely reached through the SCIT approach in the sitting position with a mean time of 14 minutes, using a basic set of microsurgical instruments. Cornerstones and potential delaying events were carefully recorded for each of the 3 main steps of the approach. Moreover, we present in a short video a step-by-step guide to perform the SCIT approach in a fast and safe way. CONCLUSIONS: A correct application of microsurgical principles may allow to safely and rapidly perform the SCIT approach, therefore offering an effective and relatively atraumatic route for dealing with pineal region lesions.
[Mh] MeSH terms primary: Cerebellum/surgery
Infratentorial Neoplasms/surgery
Microsurgery/methods
Neurosurgical Procedures/methods
Pineal Gland/surgery
Pinealoma/surgery
[Mh] MeSH terms secundary: Adolescent
Adult
Aged
Aged, 80 and over
Cerebellum/diagnostic imaging
Child
Child, Preschool
Female
Humans
Infratentorial Neoplasms/diagnostic imaging
Male
Middle Aged
Patient Positioning/methods
Pineal Gland/diagnostic imaging
Pinealoma/diagnostic imaging
Retrospective Studies
Treatment Outcome
Young Adult
[Pt] Publication type:JOURNAL ARTICLE; VIDEO-AUDIO MEDIA
[Em] Entry month:1710
[Cu] Class update date: 171003
[Lr] Last revision date:171003
[Js] Journal subset:IM
[Da] Date of entry for processing:170613
[St] Status:MEDLINE

  6 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 28215583
[Au] Autor:Flanagan ME; Williams JR; Emerson SN; Chiarelli PA; Ellenbogen RG; Cimino PJ
[Ad] Address:Department of Pathology, Division of Neuropathology, University of Washington, Seattle, WA, USA.
[Ti] Title:Clinicopathologic characteristics of metastatic esophageal carcinoma isolated to the pineal region: A case report and review of the literature.
[So] Source:Exp Mol Pathol;102(2):247-250, 2017 Apr.
[Is] ISSN:1096-0945
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:Metastasis to the pineal region is a rare event, and esophageal adenocarcinoma metastatic to the pineal region is exceptionally rare, with only two cases reported in the current literature. Here, we characterize a third case of metastatic esophageal adenocarcinoma to the pineal region, and compare clinicopathological characteristics among all three cases. The three patients were men, with ages at neurological presentation ranging from 48 to 65years. Time from initial esophageal adenocarcinoma diagnosis to development of neurologic symptoms ranged from 12 to 23months. Neuroimaging in all cases showed an isolated enhancing pineal region mass with sizes ranging from 1.8 to 2.2cm. All cases were believed to have local control of esophageal disease prior to metastatic sequela, with initial treatment including esophageal resection with or without chemoradiation therapy. No cases had evidence of primary site disease progression at time of metastatic presentation, nor were there signs of other sites of metastasis. All patients underwent tumor excision and were referred for subsequent radiotherapy. Overall, all three cases demonstrate similar demographics, histology, and clinical presentations. In the appropriate clinical setting it is important to keep esophageal metastasis in the differential diagnosis, particularly in the setting of isolated pineal lesions.
[Mh] MeSH terms primary: Adenocarcinoma/pathology
Brain Neoplasms/secondary
Esophageal Neoplasms/pathology
Pineal Gland/pathology
Pinealoma/secondary
[Mh] MeSH terms secundary: Adenocarcinoma/therapy
Aged
Brain Neoplasms/therapy
Esophageal Neoplasms/therapy
Fatal Outcome
Female
Humans
Male
Middle Aged
Pinealoma/therapy
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Entry month:1708
[Cu] Class update date: 170809
[Lr] Last revision date:170809
[Js] Journal subset:IM
[Da] Date of entry for processing:170221
[St] Status:MEDLINE

  7 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 27742368
[Au] Autor:Hakar M; Chandler JP; Bigio EH; Mao Q
[Ad] Address:Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, United States.
[Ti] Title:Neuroendocrine carcinoma of the pineal parenchyma. The first reported case.
[So] Source:J Clin Neurosci;35:68-70, 2017 Jan.
[Is] ISSN:1532-2653
[Cp] Country of publication:Scotland
[La] Language:eng
[Ab] Abstract:We report a case of a 35-year-old female patient who presented with worsening headaches, vertigo, and vision changes. MRI of the brain showed an enhancing lesion in the pineal region. The patient was taken for resection of the lesion which was classified as neuroendocrine carcinoma of the pineal parenchyma, intermediate grade. Histologically, the neoplasm was cellular, mitotically active, and composed of tightly packed cells with high nuclear cytoplasmic ratio, scant cytoplasm, and ill-defined cell borders. Immunohistochemically the tumor cells were positive for chromogranin, synaptophysin and AE1/AE3, and negative for CK-7, CK-20, and TTF1. Possible metastasis from any other primary sites was ruled out clinically. This represents the first reported case of neuroendocrine carcinoma of the pineal parenchyma.
[Mh] MeSH terms primary: Carcinoma, Neuroendocrine/diagnostic imaging
Pineal Gland/diagnostic imaging
Pinealoma/diagnostic imaging
[Mh] MeSH terms secundary: Adult
Brain/diagnostic imaging
Carcinoma, Neuroendocrine/pathology
Cell Nucleus/pathology
Cytoplasm/immunology
Female
Humans
Immunohistochemistry
Magnetic Resonance Imaging
Neoplasm Proteins/genetics
Pineal Gland/pathology
Pinealoma/pathology
Positron-Emission Tomography
Tomography, X-Ray Computed
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Nm] Name of substance:0 (Neoplasm Proteins)
[Em] Entry month:1701
[Cu] Class update date: 170123
[Lr] Last revision date:170123
[Js] Journal subset:IM
[Da] Date of entry for processing:161016
[St] Status:MEDLINE

  8 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 27282397
[Au] Autor:Raleigh DR; Solomon DA; Lloyd SA; Lazar A; Garcia MA; Sneed PK; Clarke JL; McDermott MW; Berger MS; Tihan T; Haas-Kogan DA
[Ad] Address:Department of Radiation Oncology, University of California San Francisco, San Francisco, California (D.R.R., S.A.L., A.L., M.A.G., P.K.S., D.A.H.-K.); Division of Neuropathology, Department of Pathology, University of California San Francisco, San Francisco, California (D.A.S., T.T.); Department of
[Ti] Title:Histopathologic review of pineal parenchymal tumors identifies novel morphologic subtypes and prognostic factors for outcome.
[So] Source:Neuro Oncol;19(1):78-88, 2017 Jan.
[Is] ISSN:1523-5866
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:BACKGROUND: Pineal parenchymal tumors (PPTs) are rare neoplasms of the central nervous system, and data concerning clinical outcomes are limited. The purpose of this study was to define the clinical behavior of PPT according to current histopathologic criteria and identify prognostic factors to guide therapeutic decisions. METHODS: Seventy-five patients treated for PPT at a single institution between 1992 and 2015 were retrospectively identified. Forty-five resection specimens were available and re-reviewed. Freedom from progression (FFP) and overall survival (OS) were estimated using the Kaplan-Meier method and compared using log-rank tests. RESULTS: Median follow-up was 4.1 years. All patients initially underwent surgery; 78% of patients with PPT of intermediate differentiation (PPTID) and all patients with pineoblastoma received adjuvant therapy. Pathologic re-review refined classification in 27% of cases, with the majority of these being adult patients with pineal tumors originally classified as pineoblastomas that more accurately resembled PPTID based on the 2007 WHO classification. CLASSIFICATION: Our histologic review also identified that PPTIDs can be classified into small-cell and large-cell morphologic subtypes, which have distinct clinical outcomes. Tumor grade, extent of resection, and neuraxis spread were prognostic for FFP. PPTID subtype, extent of resection, and neuraxis spread were prognostic for OS. Genetic analysis of a pineoblastoma case identified somatic mutations of DICER1, ARID1A, and KDM5C genes. CONCLUSIONS: PPTIDs can be classified into 1 of 2 novel morphologic subtypes that are associated with distinct clinical outcomes. Tumor grade, neuraxis spread, and extent of resection also influence outcome for patients with PPT.
[Mh] MeSH terms primary: Biomarkers, Tumor/genetics
Brain Neoplasms/pathology
Pineal Gland/pathology
Pinealoma/pathology
[Mh] MeSH terms secundary: Adolescent
Adult
Aged
Brain Neoplasms/genetics
Brain Neoplasms/therapy
Child
Child, Preschool
Combined Modality Therapy
Female
Follow-Up Studies
Humans
Male
Middle Aged
Mutation/genetics
Neoplasm Staging
Pineal Gland/metabolism
Pinealoma/genetics
Pinealoma/therapy
Prognosis
Retrospective Studies
Survival Rate
Young Adult
[Pt] Publication type:JOURNAL ARTICLE
[Nm] Name of substance:0 (Biomarkers, Tumor)
[Em] Entry month:1710
[Cu] Class update date: 171003
[Lr] Last revision date:171003
[Js] Journal subset:IM
[Da] Date of entry for processing:160611
[St] Status:MEDLINE
[do] DOI:10.1093/neuonc/now105

  9 / 1638 MEDLINE  
              first record previous record next record last record
select
to print
Photocopy
Full text

[PMID]: 27866682
[Au] Autor:Frappaz D; Sunyach MP; Le Rhun E; Blonski M; Laurence V; Bonneville Levard A; Loiseau H; Meyronnet D; Callies A; Laigle-Donadey F; Faure Conter C; au nom de l'ANOCEF, GO-AJA, de la SFCE
[Ad] Address:Centre Léon-Bérard, 28, Prom. Léa-et-Napoléon-Bullukian, 69008 Lyon, France; Association des neuro-oncologues d'expression française (ANOCEF), 54035 Nancy cedex, France; Société française du cancer de l'enfant (SFCE), 35203 Rennes cedex 2, France; Groupe onco-hématologie adolescents jeunes adultes (
[Ti] Title:La neuro-oncologie des adolescents et adultes jeunes (AJAS) : place d'une RCP nationale. Au nom de l'ANOCEF, GO-AJA et de la SFCE. [Adolescent and Young Adults (AYAS) brain tumor national Web conference. On behalf of ANOCEF, GO-AJA and SFCE societies].
[So] Source:Bull Cancer;103(12):1050-1056, 2016 Dec.
[Is] ISSN:1769-6917
[Cp] Country of publication:France
[La] Language:fre
[Ab] Abstract:The skills of adult versus pediatric neuro-oncologists are not completely similar though additive. Because the tumors and their protocols are different and the tolerance and expected sequelae are specific. Multidisciplinary meetings including adult and pediatric neuro-oncologists are warranted to share expertise. Since 2008, a weekly national web based conference was held in France. Any patient with the following criteria could be discussed: Adolescent and Young Adults aged between 15 and 25 years, and any adult with a pediatric type pathology, including medulloblastoma, germ cell tumors, embryonic tumors, ependymoma, pilocytic astrocytoma. RESULTS: Attendance during the year 2015 was as follows: 42 meetings were held; the median number of cases discussed at each meeting was 4 (1 to 8); the mean number of attendants was 7 (2 to 12). One hundred and sixty-eight cases concerning 121 patients were discussed. Mean age was 30 years old (7 to 67). Forty-eight percent were discussed at diagnosis. The patients had mostly medulloblastomas (40%), germ cell tumors (11%), ependymomas (11%), pineal tumors (7%) and embryonal tumors (8%). The rate of inclusion in protocols was increased since the opening of this web conference, especially for the germ cell tumor SIOP protocol that is opened without age restriction, and in RSMA standard risk or MEVITEM relapse adult medulloblastoma protocols. CONCLUSION: Multidisciplinary Web conference for AYAs is feasible and increases the inclusion rate in protocols. It should be developed further.
[Mh] MeSH terms primary: Brain Neoplasms/therapy
Interdisciplinary Communication
Medical Oncology
Neurology
Telecommunications/organization & administration
[Mh] MeSH terms secundary: Adolescent
Adult
Astrocytoma/therapy
Child
Ependymoma/therapy
Feasibility Studies
France
Humans
Medulloblastoma/therapy
Middle Aged
Neoplasms, Germ Cell and Embryonal/therapy
Pinealoma/therapy
Telecommunications/statistics & numerical data
Young Adult
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1701
[Cu] Class update date: 170131
[Lr] Last revision date:170131
[Js] Journal subset:IM
[Da] Date of entry for processing:161122
[St] Status:MEDLINE

  10 / 1638 MEDLINE  
              first record previous record
select
to print
Photocopy
Full text

[PMID]: 27712799
[Au] Autor:Causil LD; Ames R; Puac P; Castillo M
[Ad] Address:Neuroradiology Section, Department of Radiology, University of North Carolina School of Medicine, Room 3326, Old Infirmary Building, Manning Drive, Chapel Hill, NC 27599-7510, USA. Electronic address: Lazaro_causil@med.unc.edu.
[Ti] Title:Adult Brain Tumors and Pseudotumors: Interesting (Bizarre) Cases.
[So] Source:Neuroimaging Clin N Am;26(4):667-689, 2016 Nov.
[Is] ISSN:1557-9867
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Some brain tumors results are interesting due to their rarity at presentation and overwhelming imaging characteristics, posing a diagnostic challenge in the eyes of any experienced neuroradiologist. This article focuses on the most important features regarding epidemiology, location, clinical presentation, histopathology, and imaging findings of cases considered "bizarre." A review of the most recent literature dealing with these unusual tumors and pseudotumors is presented, highlighting key points related to the diagnosis, treatments, outcomes, and differential diagnosis.
[Mh] MeSH terms primary: Brain Neoplasms/diagnostic imaging
Neuroimaging/methods
Pinealoma/diagnostic imaging
Vascular Malformations/diagnostic imaging
[Mh] MeSH terms secundary: Adult
Brain/diagnostic imaging
Brain Diseases/diagnostic imaging
Diagnosis, Differential
Diagnostic Imaging/methods
Humans
Pineal Gland/diagnostic imaging
[Pt] Publication type:JOURNAL ARTICLE; REVIEW
[Em] Entry month:1703
[Cu] Class update date: 170327
[Lr] Last revision date:170327
[Js] Journal subset:IM
[Da] Date of entry for processing:161008
[St] Status:MEDLINE


page 1 of 164 go to page                         
   


Refine the search
  Database : MEDLINE Advanced form   

    Search in field  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/PAHO/WHO - Latin American and Caribbean Center on Health Sciences Information