[X] Close
You are about to erase all the values you have customized, search history, page format, etc.
Click here to RESET all values       Click here to GO BACK without resetting any value
Items 1 to 25 of about 25
1. Kaji M, Takeshima H, Nakazato Y, Kuratsu J: Low-grade astroblastoma recurring with extensive invasion. Neurol Med Chir (Tokyo); 2006 Sep;46(9):450-4
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Low-grade astroblastoma recurring with extensive invasion.
  • The histological diagnosis was low-grade astroblastoma.
  • Histological examination disclosed wide invasion by tumor cells into the subpial and perivascular space of the surrounding brain tissue.
  • Although gross total resection of astroblastoma usually results in long-term survival, some of these yet unfamiliar tumors may develop a more malignant character.
  • [MeSH-major] Brain Neoplasms / therapy. Neoplasm Recurrence, Local / therapy. Neoplasms, Neuroepithelial / therapy

  • Genetic Alliance. consumer health - Astroblastoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16998280.001).
  • [ISSN] 0470-8105
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  •  go-up   go-down


2. Mastrangelo S, Lauriola L, Coccia P, Puma N, Massimi L, Riccardi R: Two cases of pediatric high-grade astroblastoma with different clinical behavior. Tumori; 2010 Jan-Feb;96(1):160-3
MedlinePlus Health Information. consumer health - Childhood Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Two cases of pediatric high-grade astroblastoma with different clinical behavior.
  • Astroblastoma is a rare glial tumor occurring in older children and defined by histological criteria as low or high-grade.
  • We describe two children with high-grade astroblastoma.
  • The first patient, with multiple recurrences of a frontoparietal tumor, died 10 years from diagnosis after progression of the disease despite surgery, radiotherapy and chemotherapy.
  • The second patient underwent subtotal resection of a temporal mass; the residual tumor progressed five months after radiotherapy, but after a subsequent gross total resection the patient is now in complete remission 54 months from diagnosis.
  • High-grade astroblastoma is usually treated with surgery and radiotherapy, but may have an unpredictable behavior even when tumor excision is deemed complete.
  • [MeSH-major] Brain Neoplasms / diagnosis. Brain Neoplasms / therapy. Cranial Irradiation. Neoplasms, Neuroepithelial / diagnosis. Neoplasms, Neuroepithelial / therapy

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20437876.001).
  • [ISSN] 0300-8916
  • [Journal-full-title] Tumori
  • [ISO-abbreviation] Tumori
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
  •  go-up   go-down


3. Eom KS, Kim JM, Kim TY: A Cerebral Astroblastoma Mimicking an Extra-axial Neoplasm. J Korean Neurosurg Soc; 2008 Apr;43(4):205-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A Cerebral Astroblastoma Mimicking an Extra-axial Neoplasm.
  • Astroblastoma is a rarely diagnosed primary brain neoplasm whose histogenesis has been clarified recently.
  • We present a case of 20-year-old woman with an astroblastoma in the left temporal convexity that was treated with total tumor resection alone.
  • An astroblastoma should be included in the differential diagnosis of a superficially located tumor presenting with the findings of an extra-axial mass, especially in a young patient.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Neuroradiology. 2007 Mar;49(3):203-9 [17216265.001]
  • [Cites] Surg Neurol. 2007 Mar;67(3):308-13 [17320647.001]
  • [Cites] Neuropathology. 2006 Feb;26(1):72-81 [16521483.001]
  • [Cites] Childs Nerv Syst. 2005 Mar;21(3):211-20 [15654633.001]
  • [Cites] Brain Pathol. 2000 Jul;10(3):342-52 [10885653.001]
  • [Cites] J Neurosurg. 1995 Sep;83(3):550-5 [7545227.001]
  • [Cites] Neurosurgery. 1989 Jul;25(1):6-13 [2755581.001]
  • [Cites] Acta Neurochir (Wien). 2004 Jun;146(6):629-33 [15168232.001]
  • [Cites] J Neuroradiol. 1996 Jun;23(1):38-40 [8767917.001]
  • (PMID = 19096646.001).
  • [ISSN] 2005-3711
  • [Journal-full-title] Journal of Korean Neurosurgical Society
  • [ISO-abbreviation] J Korean Neurosurg Soc
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2588258
  • [Keywords] NOTNLM ; Astroblastoma / Intra-axial neoplasm
  •  go-up   go-down


Advertisement
4. Miranda P, Lobato RD, Cabello A, Gómez PA, Martínez de Aragón A: Complete surgical resection of high-grade astroblastoma with long time survival: case report and review of the literature. Neurocirugia (Astur); 2006 Feb;17(1):60-3
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Complete surgical resection of high-grade astroblastoma with long time survival: case report and review of the literature.
  • Astroblastoma is a rare glial neoplasm of unknown origin and uncertain prognosis.
  • The histological features of astroblastoma are the presence of typical astroblastic perivascular pseudorosettes and perivascular hyalinization.
  • Two different subtypes of astroblastoma have been defined based upon histological characteristics.
  • We present a new case of a patient with a high-grade astroblastoma with a long survival time, in whom complete surgical resection was confirmed by an early postoperative MRI.
  • [MeSH-major] Brain Neoplasms / surgery. Neoplasms, Neuroepithelial / surgery

  • Genetic Alliance. consumer health - Astroblastoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16565782.001).
  • [ISSN] 1130-1473
  • [Journal-full-title] Neurocirugía (Asturias, Spain)
  • [ISO-abbreviation] Neurocirugia (Astur)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 21
  •  go-up   go-down


5. Denaro L, Gardiman M, Calderone M, Rossetto M, Ciccarino P, Giangaspero F, Perilongo G, d'Avella D: Intraventricular astroblastoma. Case report. J Neurosurg Pediatr; 2008 Feb;1(2):152-5
Genetic Alliance. consumer health - Astroblastoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intraventricular astroblastoma. Case report.
  • Astroblastoma is a rare primary brain neoplasm that accounts for 0.45-2.8% of brain gliomas.
  • The authors report a case of well-differentiated completely intraventricular astroblastoma in a 6-year-old girl and review the relevant literature.
  • In patients harboring anaplastic astroblastoma, gross-total resection and adjuvant therapy after the initial surgery seems to be the best choice.
  • It is important to distinguish astroblastoma from ependymoma in clinical practice because of the differences in therapeutic approaches.
  • [MeSH-major] Cerebral Ventricle Neoplasms / diagnosis. Neoplasms, Neuroepithelial / diagnosis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18352788.001).
  • [ISSN] 1933-0707
  • [Journal-full-title] Journal of neurosurgery. Pediatrics
  • [ISO-abbreviation] J Neurosurg Pediatr
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 26
  •  go-up   go-down


6. Johnson KA, Bonnin JM, Boaz JC, Douglas-Akinwande AC, Hattab EM: Anaplastic astroblastoma presenting as massive, sudden-onset, intraparenchymal hemorrhage. Pediatr Neurosurg; 2010;46(6):457-61
MedlinePlus Health Information. consumer health - Childhood Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Anaplastic astroblastoma presenting as massive, sudden-onset, intraparenchymal hemorrhage.
  • Astroblastoma is a rare primary glial tumor of children and young adults, typically located in the cerebral hemispheres and presenting as a well-circumscribed, nodular, often cystic enhancing mass.
  • The existence of astroblastoma as a distinct clinicopathologic entity has long been debated but is recognized in the 2007 WHO classification of CNS tumors.
  • We report a case of astroblastoma with 'high-grade/anaplastic' histology in a 12-year-old, previously healthy girl.
  • The diagnosis of anaplastic astroblastoma was rendered.
  • This case illustrates the potential poor outcome of high-grade astroblastoma and highlights the morphologic heterogeneity of this rare neoplasm.
  • [MeSH-major] Brain Neoplasms / complications. Brain Neoplasms / diagnosis. Cerebral Hemorrhage / diagnosis. Cerebral Hemorrhage / etiology. Neoplasms, Neuroepithelial / complications. Neoplasms, Neuroepithelial / diagnosis

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright © 2011 S. Karger AG, Basel.
  • (PMID = 21540623.001).
  • [ISSN] 1423-0305
  • [Journal-full-title] Pediatric neurosurgery
  • [ISO-abbreviation] Pediatr Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
  •  go-up   go-down


7. Kantar M, Ertan Y, Turhan T, Kitis O, Anacak Y, Akalin T, Ersahin Y, Cetingül N: Anaplastic astroblastoma of childhood: aggressive behavior. Childs Nerv Syst; 2009 Sep;25(9):1125-9
MedlinePlus Health Information. consumer health - Childhood Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Anaplastic astroblastoma of childhood: aggressive behavior.
  • OBJECTIVE: Astroblastoma is an unusual brain tumor in childhood.
  • Histopathologically, there are two types of astroblastoma: well-differentiated (low-grade) or anaplastic (high-grade).
  • In low-grade astroblastoma, treatment of choice is complete excision.
  • Histopathologically, the tumor was an anaplastic astroblastoma.
  • However, the tumor recurred early in the course, and she died 18 months after diagnosis.
  • [MeSH-major] Brain Neoplasms / therapy. Neoplasms, Neuroepithelial
  • [MeSH-minor] Brain / pathology. Child. Fatal Outcome. Female. Humans. Magnetic Resonance Imaging. Neoplasm Recurrence, Local / diagnosis. Neoplasm Recurrence, Local / pathology. Neoplasm Recurrence, Local / therapy

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Neurosurg. 1986 Apr;64(4):657-61 [3950749.001]
  • [Cites] Pathology. 2006 Feb;38(1):78-80 [16484017.001]
  • [Cites] J Neurosurg. 1995 Sep;83(3):550-5 [7545227.001]
  • [Cites] J Neurooncol. 1998 Oct;40(1):59-65 [9874187.001]
  • [Cites] Surg Neurol. 2008 Feb;69(2):201-5 [17765957.001]
  • [Cites] J Neurooncol. 2009 Jul;93(3):369-78 [19214707.001]
  • [Cites] Acta Neurochir (Wien). 2004 Jun;146(6):629-33 [15168232.001]
  • [Cites] AJNR Am J Neuroradiol. 2002 Feb;23(2):243-7 [11847049.001]
  • [Cites] J Neurosurg Sci. 2007 Mar;51(1):21-7; discussion 27 [17369788.001]
  • [Cites] Neurocirugia (Astur). 2006 Feb;17(1):60-3 [16565782.001]
  • [Cites] Childs Nerv Syst. 2005 Mar;21(3):211-20 [15654633.001]
  • [Cites] Neurosurgery. 1989 Jul;25(1):6-13 [2755581.001]
  • [Cites] Neurol Med Chir (Tokyo). 2006 Sep;46(9):450-4 [16998280.001]
  • [Cites] J Neuroradiol. 1996 Jun;23(1):38-40 [8767917.001]
  • [Cites] Childs Nerv Syst. 2008 Feb;24(2):165-8 [17653728.001]
  • [Cites] J Neurooncol. 2007 Jul;83(3):277-8 [17332948.001]
  • [Cites] J Neurosurg Pediatr. 2008 Feb;1(2):152-5 [18352788.001]
  • [Cites] Rev Neurol. 2002 May 16-31;34(10):936-9 [12134323.001]
  • [Cites] J Korean Med Sci. 2004 Oct;19(5):772-6 [15483362.001]
  • [Cites] Neuroradiology. 2007 Mar;49(3):203-9 [17216265.001]
  • (PMID = 19357852.001).
  • [ISSN] 1433-0350
  • [Journal-full-title] Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • [ISO-abbreviation] Childs Nerv Syst
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


8. Bell JW, Osborn AG, Salzman KL, Blaser SI, Jones BV, Chin SS: Neuroradiologic characteristics of astroblastoma. Neuroradiology; 2007 Mar;49(3):203-9
Hazardous Substances Data Bank. GADOPENTETATE DIMEGLUMINE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Neuroradiologic characteristics of astroblastoma.
  • INTRODUCTION: Astroblastoma is a rare glial tumor of uncertain origin.
  • Many features previously identified are similar to those of other primary malignant brain tumors.
  • We report the largest imaging series to date and further delineate the CT and MRI features of astroblastoma.
  • We identify those features that may be useful in distinguishing astroblastoma from other neoplasms.
  • METHODS: The radiologic images, pathology reports, and clinical information of 12 patients with pathology-confirmed astroblastoma were retrospectively reviewed.
  • RESULTS: Patients ranged in age from 0 (newborn) to 50 years with a mean of 20 years at the time of initial diagnosis.
  • CONCLUSION: The imaging features of astroblastoma are identified in 12 previously unreported cases.
  • Distinguishing features that can be used to narrow the differential diagnosis with more common primary brain neoplasms reflect a combination of age, anatomic location, and specific imaging findings such as demarcation, heterogeneous tumor enhancement, rim enhancement, and a multicystic "bubbly" appearance.
  • [MeSH-major] Brain Neoplasms / diagnosis. Magnetic Resonance Imaging. Neoplasms, Neuroepithelial / diagnosis. Tomography, X-Ray Computed
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Contrast Media. Diagnosis, Differential. Female. Gadolinium DTPA. Humans. Infant. Infant, Newborn. Male. Middle Aged. Retrospective Studies


9. Ganapathy S, Kleiner LI, Mirkin DL, Broxson E: Unusual manifestations of astroblastoma: a radiologic-pathologic analysis. Pediatr Radiol; 2009 Feb;39(2):168-71
MedlinePlus Health Information. consumer health - MRI Scans.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unusual manifestations of astroblastoma: a radiologic-pathologic analysis.
  • Astroblastoma is a very rare primary glial tumor occurring in children and young adults that is almost exclusively supratentorial in location.
  • We report an extremely unusual presentation of a densely calcified posterior fossa astroblastoma with disseminated spinal and supratentorial metastasis.
  • A companion case of a low-grade astroblastoma that demonstrated classic histologic features but nonspecific and atypical imaging findings is also included.
  • [MeSH-major] Brain Stem Neoplasms / complications. Brain Stem Neoplasms / diagnosis. Calcinosis / complications. Calcinosis / diagnosis. Magnetic Resonance Imaging / methods. Neoplasms, Neuroepithelial / complications. Neoplasms, Neuroepithelial / diagnosis. Tomography, X-Ray Computed / methods
  • [MeSH-minor] Child. Female. Humans. Rare Diseases / diagnosis. Rare Diseases / etiology

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - CT Scans.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Neurooncol. 1998 Oct;40(1):59-65 [9874187.001]
  • [Cites] Surg Neurol. 2008 Feb;69(2):201-5 [17765957.001]
  • [Cites] Brain Tumor Pathol. 2008;25(1):25-31 [18415663.001]
  • [Cites] AJNR Am J Neuroradiol. 2002 Feb;23(2):243-7 [11847049.001]
  • [Cites] J Neurosurg Sci. 2007 Mar;51(1):21-7; discussion 27 [17369788.001]
  • [Cites] Childs Nerv Syst. 2005 Mar;21(3):211-20 [15654633.001]
  • [Cites] Neuropathology. 2006 Feb;26(1):72-81 [16521483.001]
  • [Cites] Neuroradiology. 2007 Mar;49(3):203-9 [17216265.001]
  • (PMID = 18958463.001).
  • [ISSN] 0301-0449
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 8
  •  go-up   go-down


10. Hata N, Shono T, Yoshimoto K, Mizoguchi M, Kawamura T, Nagata S, Matsumoto K, Hayashi K, Iwaki T, Sasaki T: An astroblastoma case associated with loss of heterozygosity on chromosome 9p. J Neurooncol; 2006 Oct;80(1):69-73
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] An astroblastoma case associated with loss of heterozygosity on chromosome 9p.
  • Here, we report an astroblastoma case in which a genetic analysis was performed.
  • Total removal of the tumor was achieved and a histological examination verified that the tumor was an astroblastoma.
  • This is the first reported case of an astroblastoma in which LOH was detected on 9p.
  • [MeSH-major] Brain Neoplasms / genetics. Chromosomes, Human, Pair 9. Neoplasms, Neuroepithelial / genetics


11. Unal E, Koksal Y, Vajtai I, Toy H, Kocaogullar Y, Paksoy Y: Astroblastoma in a child. Childs Nerv Syst; 2008 Feb;24(2):165-8
MedlinePlus Health Information. consumer health - Childhood Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Astroblastoma in a child.
  • BACKGROUND: Astroblastoma, an uncommon neuroepithelial tumor, typically presents in young adults as a well-circumscribed cortical or subcortical spherical mass.
  • Astroblastoma may cause a diagnostic problem to anyone unfamiliar with its architectural and histological features.
  • Total removal of the tumor mass was performed, and a diagnosis of high grade (malignant) variant of astroblastoma was made.
  • PROGNOSIS: The best treatment modality for astroblastoma is surgical resection if possible, whereas adjuvant therapy (radiotherapy and/or chemotherapy) can be considered in high-grade astroblastomas, with a close follow-up for all cases.
  • [MeSH-major] Brain Neoplasms / pathology. Neoplasms, Neuroepithelial / pathology

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Neurooncol. 1998 Oct;40(1):59-65 [9874187.001]
  • [Cites] Brain Pathol. 2000 Jul;10 (3):342-52 [10885653.001]
  • [Cites] Acta Neurochir (Wien). 2004 Jun;146(6):629-33 [15168232.001]
  • [Cites] AJNR Am J Neuroradiol. 2002 Feb;23(2):243-7 [11847049.001]
  • [Cites] Neurocirugia (Astur). 2006 Feb;17(1):60-3 [16565782.001]
  • [Cites] Childs Nerv Syst. 2005 Mar;21(3):211-20 [15654633.001]
  • [Cites] Neurosurgery. 1989 Jul;25(1):6-13 [2755581.001]
  • [Cites] Acta Neuropathol. 1989;78(5):472-83 [2683559.001]
  • [Cites] Neuropathology. 2006 Feb;26(1):72-81 [16521483.001]
  • (PMID = 17653728.001).
  • [ISSN] 1433-0350
  • [Journal-full-title] Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • [ISO-abbreviation] Childs Nerv Syst
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


12. Kubota T, Sato K, Arishima H, Takeuchi H, Kitai R, Nakagawa T: Astroblastoma: immunohistochemical and ultrastructural study of distinctive epithelial and probable tanycytic differentiation. Neuropathology; 2006 Feb;26(1):72-81
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Astroblastoma: immunohistochemical and ultrastructural study of distinctive epithelial and probable tanycytic differentiation.
  • We report the clinicopathological findings of astroblastoma found in an 8-year-old girl who was subsequently treated for 11 years.
  • The tumor cells showed typical features of astroblastoma comprising prominent perivascular pseudorosettes with remarkable vascular sclerosis.
  • We report these unique histological features, and stress that astroblastoma should be categorized as a specific type of neuroepithelial tumor.
  • [MeSH-major] Brain Neoplasms / ultrastructure. Epithelial Cells / pathology. Neoplasms, Neuroepithelial / ultrastructure
  • [MeSH-minor] Biomarkers, Tumor / analysis. Cell Lineage. Child. Diagnosis, Differential. Female. Glioma / pathology. Humans. Immunohistochemistry. Magnetic Resonance Imaging. Microscopy, Electron, Transmission

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • MedlinePlus Health Information. consumer health - Childhood Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16521483.001).
  • [ISSN] 0919-6544
  • [Journal-full-title] Neuropathology : official journal of the Japanese Society of Neuropathology
  • [ISO-abbreviation] Neuropathology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  •  go-up   go-down


13. Scheithauer BW, Aker AT, Ketterling RP, Carlson AW, Knudson RA, Tyler M: Anaplastic astroblastoma-sarcoma in neurofibromatosis Type 1. Clin Neuropathol; 2010 Sep-Oct;29(5):289-96
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Anaplastic astroblastoma-sarcoma in neurofibromatosis Type 1.
  • Astroblastoma is a distinctive brain tumor when its histologic features occur in pure form.
  • Astroblastoma as a de novo component of gliosarcoma has not previously been described.
  • Furthermore, astroblastoma has only once been reported to occur in the setting of neurofibromatosis Type I (NF1), a condition more often associated with pilocytic and diffuse or infiltrative astrocytic tumors.
  • Herein, we describe a unique case of anaplastic de novo astroblastoma-sarcoma, in essence a variant of gliosarcoma, occurring in a 50-year-old female with documented NF1.
  • The latter alterations, having been reported in astroblastoma, were noted in both tumor components, thus confirming the common origin of the glial and sarcomatous elements.
  • [MeSH-major] Brain Neoplasms / diagnosis. Neoplasms, Neuroepithelial / diagnosis. Neurofibromatosis 1 / diagnosis. Sarcoma / diagnosis
  • [MeSH-minor] Brain / pathology. Chromosome Aberrations. Comorbidity. Female. Humans. Middle Aged. PTEN Phosphohydrolase / genetics. Sequence Deletion / genetics


14. Notarianni C, Akin M, Fowler M, Nanda A: Brainstem astroblastoma: a case report and review of the literature. Surg Neurol; 2008 Feb;69(2):201-5
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Brainstem astroblastoma: a case report and review of the literature.
  • BACKGROUND: Astroblastoma is a rare glial tumor that occurs mainly in the cerebral hemispheres of young adults.
  • Our purpose in writing this article is to report one case of astroblastoma located within the medulla and review the literature on this infrequent tumor.
  • METHODS: One case of astroblastoma was retrospectively reviewed.
  • CONCLUSIONS: The combination of the radiologic and histopathologic characteristics of this tumor is necessary for making the diagnosis of astroblastoma.
  • [MeSH-major] Brain Stem Neoplasms / diagnosis. Neoplasms, Neuroepithelial / diagnosis

  • Genetic Alliance. consumer health - Astroblastoma.
  • COS Scholar Universe. author profiles.
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17765957.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 21
  •  go-up   go-down


15. Mangano FT, Bradford AC, Mittler MA, Valderrama E, Schneider SJ: Astroblastoma. Case report, review of the literature, and analysis of treatment strategies. J Neurosurg Sci; 2007 Mar;51(1):21-7; discussion 27
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Astroblastoma. Case report, review of the literature, and analysis of treatment strategies.
  • Astroblastoma, a unique glial tumor, has been described in the literature in case reports and small series.
  • Imaging studies of the brain demonstrated a large heterogeneously enhancing solid mass in the left frontal lobe with punctate calcifications and cystic components that created subfalcine and uncal herniation.
  • After tumor resection, histological diagnosis revealed a high-grade cerebral astroblastoma.
  • Since the first description of astroblastoma, its histopathological and clinical features have been debated.
  • We review the histology, immunohistochemistry, and cytogenetics of astroblastoma as well as examine the current literature and treatment strategies for the management of both low and high-grade tumors.
  • [MeSH-major] Brain Neoplasms / pathology. Brain Neoplasms / physiopathology. Frontal Lobe / pathology. Frontal Lobe / physiopathology. Neoplasms, Neuroepithelial / pathology. Neoplasms, Neuroepithelial / physiopathology
  • [MeSH-minor] Age Factors. Biomarkers, Tumor / analysis. Biomarkers, Tumor / metabolism. Brain Edema / etiology. Brain Edema / physiopathology. Child. Chromosome Aberrations. DNA Mutational Analysis. Humans. Hydrocephalus / etiology. Hydrocephalus / physiopathology. Hydrocephalus / therapy. Intracranial Hypertension / etiology. Intracranial Hypertension / pathology. Intracranial Hypertension / physiopathology. Magnetic Resonance Imaging. Male. Neurosurgical Procedures. Postoperative Complications / etiology. Postoperative Complications / physiopathology. Postoperative Complications / therapy. Radiotherapy. Tomography, X-Ray Computed. Treatment Outcome. Ventriculoperitoneal Shunt

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • MedlinePlus Health Information. consumer health - Childhood Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17369788.001).
  • [ISSN] 0390-5616
  • [Journal-full-title] Journal of neurosurgical sciences
  • [ISO-abbreviation] J Neurosurg Sci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  •  go-up   go-down


16. Tumialán LM, Brat DJ, Fountain AJ, Barrow DL: An astroblastoma mimicking a cavernous malformation: case report. Neurosurgery; 2007 Mar;60(3):E569-70; discussion E570
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] An astroblastoma mimicking a cavernous malformation: case report.
  • An astroblastoma was diagnosed after resection and neuropathological examination.
  • CONCLUSION: A rare radiological to pathological correlation of astroblastoma is presented in which the evolving hematoma, as observed on magnetic resonance imaging scans, complicated the radiographic diagnosis of this lesion.
  • [MeSH-major] Brain Neoplasms / radiography. Brain Neoplasms / surgery. Hemangioma, Cavernous, Central Nervous System / radiography. Hematoma, Epidural, Cranial / radiography. Hematoma, Epidural, Cranial / surgery. Neoplasms, Neuroepithelial / radiography. Neoplasms, Neuroepithelial / surgery
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans

  • Genetic Alliance. consumer health - Astroblastoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17327764.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


17. Salvati M, D'Elia A, Brogna C, Frati A, Antonelli M, Giangaspero F, Raco A, Santoro A, Delfini R: Cerebral astroblastoma: analysis of six cases and critical review of treatment options. J Neurooncol; 2009 Jul;93(3):369-78
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cerebral astroblastoma: analysis of six cases and critical review of treatment options.
  • Astroblastoma is one of the rarest tumors of the central nervous system (CNS), and its classification, histogenesis, diagnosis and therapeutic management are still being debated.
  • To clarify the clinical, radiological, histopathological, prognostic and therapeutic characteristics, which have been treated only recently and are not well established yet due to the rarity of this tumor, six cases of histologically proven astroblastoma were retrospectively analyzed in light of more pertinent literature and paying special attention to therapeutic remarks.
  • Between 1996 and 2005, six patients with cerebral astroblastoma were surgically treated at the Department of Neurosciences-Neurosurgery of Sapienza University in Rome.
  • In three cases the lesion was termed low-grade astroblastoma, and high grade in the other three, according to current standard parameters.
  • The time to diagnosis ranged from 1 week to 18 months.
  • The three patients with low-grade astroblastoma are still alive today after a follow-up of 2, 5 and 19 years, respectively.
  • We propose an aggressive standardized treatment for those lesions that meet anaplastic criteria, owing to their postulated glial origin and the propensity to have aggressive courses, and we advocate the use of a safe adjuvant chemotherapeutic regimen with TMZ, used concomitantly and subsequently to radiotherapy, especially for the high-grade astroblastoma cases.
  • [MeSH-major] Brain Neoplasms / pathology. Brain Neoplasms / therapy. Neoplasms, Neuroepithelial / pathology. Neoplasms, Neuroepithelial / therapy

  • Genetic Alliance. consumer health - Astroblastoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Surg Neurol. 1985 Aug;24(2):218-22 [4012581.001]
  • [Cites] J Neurosurg. 1986 Apr;64(4):657-61 [3950749.001]
  • [Cites] Pathology. 2006 Feb;38(1):78-80 [16484017.001]
  • [Cites] Acta Neuropathol. 2016 Jun;131(6):803-20 [27157931.001]
  • [Cites] J Neurosurg. 1995 Sep;83(3):550-5 [7545227.001]
  • [Cites] J Neurooncol. 1998 Oct;40(1):59-65 [9874187.001]
  • [Cites] AJNR Am J Neuroradiol. 1993 Jul-Aug;14 (4):946-50 [8352168.001]
  • [Cites] Brain Pathol. 2000 Jul;10 (3):342-52 [10885653.001]
  • [Cites] Acta Neurochir (Wien). 2004 Jun;146(6):629-33 [15168232.001]
  • [Cites] Comput Med Imaging Graph. 2002 May-Jun;26(3):187-91 [11918982.001]
  • [Cites] AJNR Am J Neuroradiol. 2002 Feb;23(2):243-7 [11847049.001]
  • [Cites] Surg Neurol. 1991 Feb;35(2):116-21 [1990478.001]
  • [Cites] Ultrastruct Pathol. 1999 Sep-Oct;23(5):325-32 [10582270.001]
  • [Cites] Neuropathology. 2000 Sep;20(3):228-32 [11132940.001]
  • [Cites] Clin Neurol Neurosurg. 1975;78(2):89-98 [1222508.001]
  • [Cites] Neurosurgery. 1989 Jul;25(1):6-13 [2755581.001]
  • [Cites] Acta Neuropathol. 1986;70(1):10-6 [3727930.001]
  • [Cites] J Neuroradiol. 1996 Jun;23(1):38-40 [8767917.001]
  • [Cites] Pediatr Pathol. 1993 May-Jun;13(3):323-32 [8516227.001]
  • [Cites] Acta Neuropathol. 1989;78(5):472-83 [2683559.001]
  • [Cites] Cancer. 1985 Feb 15;55(4):745-50 [3967170.001]
  • [Cites] Genes Chromosomes Cancer. 1996 Apr;15(4):199-205 [8703845.001]
  • (PMID = 19214707.001).
  • [ISSN] 1573-7373
  • [Journal-full-title] Journal of neuro-oncology
  • [ISO-abbreviation] J. Neurooncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 34
  •  go-up   go-down


18. Huhn SL, Yung Y, Cheshier S, Harsh G, Ailles L, Weissman I, Vogel H, Tse V: Identification of phenotypic neural stem cells in a pediatric astroblastoma. J Neurosurg; 2005 Nov;103(5 Suppl):446-50
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Identification of phenotypic neural stem cells in a pediatric astroblastoma.
  • OBJECT: The goal of this study was to illustrate the findings of a significant subpopulation of cells within a pediatric astroblastoma that have the specific cell surface phenotype found on known human neural stem cells.
  • METHODS: Cells with a cell surface marker profile characteristic of human neural stem cells were isolated using fluorescence-activated cell sorting from a mostly nonmitotic astroblastoma removed from the brain of an 11-year-old girl.
  • CONCLUSIONS: Although this astroblastoma contained a high proportion of phenotypic neural stemlike cells, the cells had limited proliferative capacity and multipotency.
  • Their role in astroblastoma formation and growth is unknown.
  • [MeSH-major] Antigens, CD / analysis. Brain Neoplasms / pathology. Neoplasms, Neuroepithelial / pathology. Stem Cells


19. Alaraj A, Chan M, Oh S, Michals E, Valyi-Nagy T, Hersonsky T: Astroblastoma presenting with intracerebral hemorrhage misdiagnosed as dural arteriovenous fistula: review of a rare entity. Surg Neurol; 2007 Mar;67(3):308-13
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Astroblastoma presenting with intracerebral hemorrhage misdiagnosed as dural arteriovenous fistula: review of a rare entity.
  • BACKGROUND: Astroblastoma is one of the most unusual types of tumors whose histogenesis has been recently clarified.
  • The lesion was resected, and pathology showed a GFAP-positive lesion with prominent astroblastoma rosettes.
  • Because of its high degree of proliferation, the presence of astroblastic pseudorosettes, prominent perivascular hyalinization, regional hyaline changes, and pushing borders with regard to the adjacent brain, the tumor was considered anaplastic.
  • CONCLUSIONS: Astroblastoma is a rare pure pathologic entity--a distinct form of astrocytic gliomas.
  • The diagnosis of astroblastoma is often difficult because of the astroblastic aspects that can be found in astrocytic tumors, in ependymomas, and in nonneuroepithelial tumors.
  • [MeSH-major] Central Nervous System Vascular Malformations / diagnosis. Cerebral Hemorrhage. Diagnostic Errors. Neoplasms, Neuroepithelial
  • [MeSH-minor] Adult. Cerebral Angiography. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male. Neoplasm Staging

  • Genetic Alliance. consumer health - Astroblastoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17320647.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


20. Fathi AR, Novoa E, El-Koussy M, Kappeler A, Mariani L, Vajtai I: Astroblastoma with rhabdoid features and favorable long-term outcome: report of a case with a 12-year follow-up. Pathol Res Pract; 2008;204(5):345-51
Hazardous Substances Data Bank. DACARBAZINE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Astroblastoma with rhabdoid features and favorable long-term outcome: report of a case with a 12-year follow-up.
  • Astroblastoma is a historically traded microscopic diagnosis to denote a rare neuroepithelial tumor of uncertain nosology, involving a distinctive pattern of pseudorosette arrangement of neoplastic cells.
  • We report on clinicopathologic correlations in a case of astroblastoma involving an extensive rhabdoid phenotype of tumor cells.
  • A review of pathology samples from both surgeries showed well-differentiated astroblastoma according to current standards, with an MIB-1 labeling index of 1% and 4%, respectively.
  • [MeSH-major] Brain Neoplasms / pathology. Neoplasm Recurrence, Local. Neoplasms, Neuroepithelial / pathology. Parietal Lobe / pathology. Rhabdoid Tumor / pathology

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18280055.001).
  • [ISSN] 0344-0338
  • [Journal-full-title] Pathology, research and practice
  • [ISO-abbreviation] Pathol. Res. Pract.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Antibodies, Antinuclear; 0 / Antibodies, Monoclonal; 0 / Antineoplastic Agents, Alkylating; 0 / Glial Fibrillary Acidic Protein; 0 / Ki-67 Antigen; 0 / MIB-1 antibody; 0 / Vimentin; 7GR28W0FJI / Dacarbazine; 85622-93-1 / temozolomide
  •  go-up   go-down


21. Navarro R, Reitman AJ, de León GA, Goldman S, Marymont M, Tomita T: Astroblastoma in childhood: pathological and clinical analysis. Childs Nerv Syst; 2005 Mar;21(3):211-20
Genetic Alliance. consumer health - Astroblastoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Astroblastoma in childhood: pathological and clinical analysis.
  • METHODS: Eight children with astroblastomas of the brain were examined.
  • Diagnosis was based on cell morphology, vascular attachment of the cell main process, lack of an epithelial-free surface differentiation, and poor intercellular cohesiveness.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Surg Neurol. 1985 Aug;24(2):218-22 [4012581.001]
  • [Cites] J Neurosurg. 1986 Apr;64(4):657-61 [3950749.001]
  • [Cites] J Neurosurg. 1995 Sep;83(3):550-5 [7545227.001]
  • [Cites] J Neurooncol. 1998 Oct;40(1):59-65 [9874187.001]
  • [Cites] No Shinkei Geka. 1982 Mar;10(3):291-3 [7099371.001]
  • [Cites] AJNR Am J Neuroradiol. 1993 Jul-Aug;14 (4):946-50 [8352168.001]
  • [Cites] Brain Pathol. 2000 Jul;10 (3):342-52 [10885653.001]
  • [Cites] Z Zellforsch Mikrosk Anat. 1954;39(6):588-617 [13206296.001]
  • [Cites] J Neuropathol Exp Neurol. 1983 May;42(3):256-67 [6302229.001]
  • [Cites] AJNR Am J Neuroradiol. 2002 Feb;23(2):243-7 [11847049.001]
  • [Cites] Neurocirugia (Astur). 2002 Oct;13(5):378-84; discussion 384 [12444409.001]
  • [Cites] Surg Neurol. 1991 Feb;35(2):116-21 [1990478.001]
  • [Cites] Ultrastruct Pathol. 1999 Sep-Oct;23(5):325-32 [10582270.001]
  • [Cites] Neuropathology. 2000 Sep;20(3):228-32 [11132940.001]
  • [Cites] Neuropathol Appl Neurobiol. 2000 Jun;26(3):295-8 [10886687.001]
  • [Cites] J Neurooncol. 1988;6(1):9-23 [3294353.001]
  • [Cites] Clin Neurol Neurosurg. 1975;78(2):89-98 [1222508.001]
  • [Cites] Neurosurgery. 1989 Jul;25(1):6-13 [2755581.001]
  • [Cites] Acta Neuropathol. 1986;70(1):10-6 [3727930.001]
  • [Cites] Am J Clin Pathol. 1969 Dec;52(6):741-4 [5353841.001]
  • [Cites] J Neuroradiol. 1996 Jun;23(1):38-40 [8767917.001]
  • [Cites] Acta Neuropathol. 1986;69(1-2):23-7 [3962596.001]
  • [Cites] Pediatr Pathol. 1993 May-Jun;13(3):323-32 [8516227.001]
  • [Cites] Acta Neuropathol. 1989;78(5):472-83 [2683559.001]
  • [Cites] Cancer. 1985 Feb 15;55(4):745-50 [3967170.001]
  • [Cites] No To Shinkei. 1969 Jun;21(6):610-3 [5820332.001]
  • (PMID = 15654633.001).
  • [ISSN] 0256-7040
  • [Journal-full-title] Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • [ISO-abbreviation] Childs Nerv Syst
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


22. Hirano H, Yunoue S, Kaji M, Tsuchiya M, Arita K: Consecutive histological changes in an astroblastoma that disseminated to the spinal cord after repeated intracranial recurrences: a case report. Brain Tumor Pathol; 2008;25(1):25-31
MedlinePlus Health Information. consumer health - Brain Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Consecutive histological changes in an astroblastoma that disseminated to the spinal cord after repeated intracranial recurrences: a case report.
  • After the third surgery, this case was reported as a low-grade astroblastoma that is characterized by perivascular pseudorosettes consisting of elongated tumor cells arranged around the blood vessels.
  • However, the fourth and fifth surgical specimens demonstrated very interesting histological changes in the astroblastoma.
  • [MeSH-major] Brain Neoplasms / pathology. Neoplasms, Neuroepithelial / secondary. Spinal Cord Neoplasms / secondary

  • Genetic Alliance. consumer health - Astroblastoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18415663.001).
  • [ISSN] 1433-7398
  • [Journal-full-title] Brain tumor pathology
  • [ISO-abbreviation] Brain Tumor Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Glial Fibrillary Acidic Protein; EC 4.2.1.11 / Phosphopyruvate Hydratase
  •  go-up   go-down


23. Lehman NL: Central nervous system tumors with ependymal features: a broadened spectrum of primarily ependymal differentiation? J Neuropathol Exp Neurol; 2008 Mar;67(3):177-88
MedlinePlus Health Information. consumer health - Stem Cells.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Several other CNS tumor entities, including astroblastoma, chordoid glioma, papillary tumor of the pineal region, angiocentric glioma, and pilomyxoid astrocytoma, variably display histopathologic features of ependymal differentiation.
  • [MeSH-minor] Biomarkers, Tumor / genetics. Biomarkers, Tumor / metabolism. Diagnosis, Differential. Humans

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18344909.001).
  • [ISSN] 0022-3069
  • [Journal-full-title] Journal of neuropathology and experimental neurology
  • [ISO-abbreviation] J. Neuropathol. Exp. Neurol.
  • [Language] eng
  • [Grant] United States / NINDS NIH HHS / NS / K08 NS45077
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  • [Number-of-references] 81
  •  go-up   go-down


24. Fan YS, Lui PC, Tam FK, Hung KN, Ng HK, Leung SY: A 33-year-old Chinese woman with a left frontal tumor. Brain Pathol; 2009 Apr;19(2):337-40
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Rhabdoid tumor cells are typically observed in atypical teratoid/rhabdoid tumor (AT/RT) but may also be seen in meningioma,glioma, melanoma, rhabdomyosarcoma and metastatic carcinoma.We present an astroblastoma with unusual rhabdoid features which is rarely described in the English literature.
  • Apart from the rhabdoid tumor cells, all the histopathological features typical for astroblastoma are present in this case.
  • The diagnosis of astroblastoma is also well supported by the age of presentation, anatomical location and radiological features of the tumor.We believe that on top of the above-mentioned unusual tumors with rhabdoid cells, astroblastoma should also be considered in the list of differential diagnosis.
  • [MeSH-major] Brain Neoplasms / pathology. Frontal Lobe. Neoplasms, Neuroepithelial / pathology

  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19291001.001).
  • [ISSN] 1750-3639
  • [Journal-full-title] Brain pathology (Zurich, Switzerland)
  • [ISO-abbreviation] Brain Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
  •  go-up   go-down


25. Bannykh SI, Fan X, Black KL: Malignant astroblastoma with rhabdoid morphology. J Neurooncol; 2007 Jul;83(3):277-8
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Malignant astroblastoma with rhabdoid morphology.
  • [MeSH-major] Brain Neoplasms / pathology. Neoplasms, Neuroepithelial / pathology. Rhabdoid Tumor / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male

  • Genetic Alliance. consumer health - Astroblastoma.
  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17332948.001).
  • [ISSN] 0167-594X
  • [Journal-full-title] Journal of neuro-oncology
  • [ISO-abbreviation] J. Neurooncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
  •  go-up   go-down






Advertisement