A Case Report Of Rare Location Of Ganglioglioma

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Desmoplastic Infantile Ganglioglioma/Astrocytoma (DIG/DIA

Aug 01, 2018 P14ARF gene were seen in one case (32). Lonnrot and colleagues, identified MYCN amplifications in 2 cases and EGFR amplifica-tions in 3 cases (39). Several negative TP53 analyses in patients withDIG/DIAhavebeenperformed(7,31,32,39,40),with1case report of a TP53 SNV found in both a primary DIG and in its subsequent malignant transformation (22).

Desmoplastic Non-Infantile Ganglioglioma; An Incidental

desmoplastic ganglioglioma: a report of 2 cases. Pediatr Radiol 36(6): 541-545. 10. Khubchandani SR, Chitale AR, Doshi PK (2009) Desmoplastic non-infantile ganglioglioma: A low-grade tumor, report of two patients. Neurol India 57(6): 796-799.

Case Report Supratentorial Intracerebral Schwannoma : Its

cytic astrocytoma, ganglioglioma, pleomorphic xanthoastrocy-toma, and dysembryoplastic neuroepithelial tumor, with radio-graphic evidence only. Large intraparenchymal schwannomas have been mistaken for meningioma or high-grade glioma11,14). Our case appears to share many of the previously described typical features of intracerebral schwannoma.

Malignant Transformation of a Desmoplastic Infantile

We describe a rare case of desmoplastic infantile ganglioglioma that appears to have transformed into a glioblastoma multiforme tumor in a 5-year-old girl. The patient was initially treated with total removal of the tumor, without subsequent radiation therapy or chemotherapy. She was in good health for 3 years,

Ganglion cell choristoma of the deep branch of the radial

Ganglioglioma of the neurohypophysis. Endocr Pathol 2008;19:112 6. 6 Sharma MC, Karak AK, Mahapatra AK, et al. Pituitary adenoma with neuronal choristoma: a report of two rare cases. Clin Neurol Neurosurg 1999;101:128 32. 7 Rios JJ, Diaz-Cano SJ, Rivera-Hueto F, et al. Cutaneous ganglion cell choristoma. Report of a case. J Cutan Pathol

Ganglioglioma of the Optic Chiasm: Case Report and Review of

Summary: We report a case of a hypothalamic chiasmatic ganglioglioma in a 21-year-old woman who presented with hyperprolactinemia and developed visual field defects. This circumscribed cystic lesion with an enhancing mural nod-ule was radiologically indistinguishable from a pilocytic as-trocytoma. Although rare, gangliogliomas should be in-

Intraparenchymal Choroid Plexus Papilloma: A Case Report and

Case Report. Intraparenchymal Choroid Plexus Papilloma: A Case Report and Literature Review. Cheng-Che Hung, I-Han Hsiao, Chun-Chung Chen* and Der-Yang Cho. Department of Neurosurgery, China Medical University Hospital, Taiwan. Abstract. Choroid plexus papilloma (CPP) is a rare tumor of the central nervous system,

Case Report Ganglioglioma in Brainstem : Case Report and a

Ganglioglioma in Brainstem : Case Report and a Review of Literatures Infratentorial ganglioglioma is a very rare entity with a rare location. Nevertheless, ganglioglioma should be included in the

Cerebellopontine Angle Ganglioglioma: MR Findings

stem, and optic nerve (3). The common location of ganglioglioma is the temporal lobe, and other lo-cations are the frontal, parietal, and occipital lobes. We present the MR imaging findings of a case of a cerebellopontine (CP) angle ganglioglioma. Case Report A 2-year-old boy was brought to the hospital because of developmental delay.

Rare Case of a Bronchial Endodermal Cyst of the Cauda Equina

2. Establish a differential diagnostic approach based on location and imaging patterns; 3. Discuss neurenteric cysts of the spine; 4. Present a rare case of a bronchial endodermal cyst of the caudal equina.

Cerebellar Ganglioglioma in Childhood: Histopathologic

We report the case of a 19-year-old female with cere-bellar ganglioglioma that was diagnosed at 4 years of age. Despite treatment with partial resection, radiation, and chemotherapy, residual tumor slowly expanded into the brainstem and upper cervical cord, resulting in noc-turnal hypopnea, progressive tetraparesis, and feeding

CASE REPORT Atypical Teratoid/Rhabdoid Tumor of the Spine

CASE REPORT Atypical Teratoid/Rhabdoid Tumor of the Spine K.K. Moeller S. Coventry S. Jernigan T.M. Moriarty SUMMARY: Atypical teratoid/rhabdoid tumor (AT/RT) is a highly malignant central nervous system neoplasm usually seen in young children and infants. Prognosis for AT/RT is poor, with most patients dying within 1 year of presentation.

Anaplastic Ganglioglioma of the Pineal Region ACaseReport

case, we employed adjuvant therapy based on current treatment standards for other high-grade gliomas aimed at an extended recurrence-free survival. Conclusion This reportdescribes avery rare case ofa 32-year-oldwoman with anaplastic ganglioglioma of the pineal region, which tested negative for biomarkers. The surgical approach

Case Gangliogliomas: A Report of Five Cases

Although the most frequent intracranial location of the ganglioglioma is the temporal lobe, other locations in order of frequency include frontal, parietal and occipital lobes.8 Brain stem and spinal cord are also involved.9 Intraventricular location is rare for gangliogliomas.3 In our series 2 cases were situated in the parietal lobe, one


location in the cerebral hemispheres and involvement of the meninges [1]. Although there have been case reports on PXA of other sites (e.g. uncal, cerebellum) and some reports have an older age distrubition [2,3]. Many patients have a long history of seizures (epilepsy is a common clinical feature) because of the superficial, cortical location.

Ganglioglioma Arising From Desmoplastic Medulloblastoma: A

Feb 22, 2017 medulloblastoma. This case raises the possibility that a malignant medulloblastoma can differentiate into a benign tumor and suggests that differentiation therapy may have value in the treatment of medulloblastoma. PEDIATRICS Volume 139 , number 3 , March 2017 :e 20161403 CASE REPORT To cite: Valvi S and Ziegler DS. Ganglioglioma


cribesthis rare entity.1 Dysplastic cerebellar ganglio-cytoma is seen most frequently in young adults i.e. third or fourth decade of life with an average age of 34 years.1,2 Less frequently, it occurs in pediatric group.2 There is no sex predilection. We report a rare case of Lhermitte-Duclos disease in a young male patient.

279 Intractable & Rare Diseases Research. 2019; 8(4):279-282

Intractable & Rare Diseases Research. 2019; 8(4):279-282. high-grade glioneuronal tumors so far in the literature. Here, we discuss a case of glioneuronal tumor with anaplasia and KIAA1549/BRAF fusion. 2. Case Report 2.1. Clinical history A ten-year-old boy presented to hospital with one year of headache and three months of blurry vision and

Desmoplastic infantile ganglioglioma - A case report

positivity. Desmoplastic infantile ganglioglioma is a rare tumor of infancy, which has excellent prognosis after total exci-sion. No adjuvant therapy is required. This is the first Indian report of desmoplastic infantile ganglioglioma out of less than fifty cases reported worldwide. Key Words: Desmoplastic infantile ganglioglioma, supraten-

Case Report

ganglioglioma (ganglion cell-giant cell glioblastoma): a case report and review of the literature.Arch Pathol Lab Med 4: 342 345, 1999 6) Haddad SF, Moore SA, Menezes AH, Van Gilder JC: Ganglioglioma: 13 years of experience. Neurosurgery 31: 171 178, 1992 7) Hakim R, Loeffler JS, Anthony DC, Black PM: Gangliogliomas in adults. Cancer 79

Cheng et al. Cystoid angiocentric glioma: A case report and

Radiology Case. 2015 Jul; 9(7):1-9 :: DOI: 10.3941/jrcr.v9i7.2413 Angiocentric glioma is a rare subtype of neuroepithelial tumor that is associated with a history of epilepsy. We report a case of cystoid angiocentric glioma associated with an area of calcification. This 25 year old

8 Case Report Anaplastic ganglioglioma originating from the

Abstract: Ganglioglioma (GG) is a rare kind of intracranial tumor with low potential malignancy (WHO grade I), which could occur in any part of the brain. However, a patient with anaplastic ganglioglioma (WHO grade III) in the medulla oblongata is a more peculiar and rare clinical case. In our report, we presented a

Cerebellar ganglioglioma in a young woman

Open Access Case Report ISSN: 2641-0362 Introduction Ganglioglioma is a very uncommon primary neoplasm of the central nervous system, most commonly found in the supratentorial compartment. Occurrence in the posterior fossa is extremely rare. Moreover most reported cases concern children. No previous reports have compared the imaging semiology of

Purely Cystic Desmoplastic Ganglioglioma: An Incidental

tures of desmoplastic ganglioglioma. Hence, the current case is reporting the rare histologic finding of cystic change in desmoplastic ganglioglioma. Case Report A 12-month-old infant was referred to neurosurgery out patient department from pediatrics department with histo-ry of developmental delay and a large cyst on the right side

Case Report A Rare Case of Concomitant Intramedullary

Ganglioglioma of the brainstem : report of three cases and review of the literature. Surg Neurol 56 : 315-322; discussion 322-324, 2001 10. Milligan BD, Giannini C, Link MJ : Ganglioglioma in the cerebellopon-tine angle in a child. Case report and review of the literature. J Neuro-surg 107 (4 Suppl) : 292-296, 2007 11.

A case report of rare location of ganglioglioma

CASE REPORT Open Access A case report of rare location of ganglioglioma Vikas Sharma1*, S. Bhaskar2, Sumit Ramdas Hire2 and Arvind Ahuja3 Abstract Background: Gangliogliomas are rare tumors of the centralnervous system. They can occur anywhere in the central nervous system but are most commonly located in the temporal lobe and are mainly found

Subependymal giant cell astrocytoma (SEGA): a case report and

Case presentation: We report a case of subependymal giant cell astrocytoma in a 10-year-old white girl, who had no clinical symptoms of tuberous sclerosis. A computed tomography scan revealed a voluminous mass in her perilateral ventricle. An extemporaneous examination was in favor of a benign ganglioglioma tumor. After fixation in 10 % neutral-

Ganglioglioma of Conus Medullaris A Rare Case

Their location in the spinal cord is rare.1-4 Usually they are intramedullary, and exophytic extension is very rare. It is because of this rare location that this case is being reported. Case Report An 11-year-old boy was admitted with complaints of pain, weakness of the right lower limb, and difficulty in walking of

case report Desmoplastic Infantile Ganglioglioma Masquerading

desmoplastic infantile ganglioglioma (dIG) is a rare supratentorial brain tumor, which is usually diagnosed before the age of two and has a favorable prognosis. o date, only t a few cases have been reported in the literature. We report a case of dIG in a three-month-old boy who presented to our pediatric emergency department with decreased

Successful Treatment With Dabrafenib (GSK2118436) in a

Wetmore C: Location, location, location: Gene expression studies of brainstem ganglioglioma A rare tumor in a very rare location. Pediatr Blood Cancer 59:1153-1154, 2012 2. Luyken C, Blu¨mcke I, Fimmers R, et al: Supratentorial gangliogliomas: Histopathologic grading and tumor recurrence in 184 patients with a median follow-up of 8 years.

Former DNB Resident at Apollo Hospital Bangalore, with

Ganglioglioma is one of the common tumour responsible for refractory temporal lobe epilepsy in children and young adults. Positioned in the group glioneural tumours, it is mostly of low grade histology. Here we outline a rare case of intraventricular ganglioglioma at atypical location with atypical morphology, lacking its most

Primary atypical teratoid/rhabdoid tumor of the optic nerve

2006, Allen et al. described a case of an AT/RT of the optic nerve secondarily arising in a ganglioglioma [14]. Verma et al. reported in 2008 a case of primary AT/RT in optic nerve in 2-years-old boy [15]. In addition, Fujita et al. reported in 2005 a case of multicentric AT/RTs occurring in the eye and fourth ventricle but without involvement of

Rare and Unusual Case of Intramedullary Spinal Cord Neurofibroma

ganglioglioma. The Ki-67/MIB1 proliferation index was less than 2%, consistent with an indolent lesion (Figure 2D). The immune profile was in keeping with the diagnosis of neurofibroma. This case was reviewed by two neuropathologists who agreed with the rendered diagnosis. DISCUSSION Neurofibromas and schwannomas belong to family of a

Case Report - researchgate.net

Case Report Brainstem ganglioglioma in an infant: Case Brainstem location has been reported infrequently. As with cortically based we present a rare case of a brainstem ganglioglioma in an

Cervicomedullary Ganglioglioma in a Child A Case Report

Abstract: Ganglioglioma is a benign slow-growing neoplasm that most frequently occurs at the supratentorial region. Nevertheless, there are occasional reports of ganglioglioma occurring in the brainstem and spinal cord. Here we report a rare case of the craniocervical ganglioglioma. A 3.5-year-old male, presented with

Calcified Cerebellar Ganglioglioma in an Adult Patient: Case

Ganglioglioma originating in the cerebellum with a large cyst a case report and review of the literature. Clin Neuropathol. 2008;27(6):369-72. 12. Mizuno J, Nishio S, Barrow DL, Davis PC, Tindall GT. Ganglioglioma of the cerebellum: case report. Neurosurgery. 1987;21(4):584-8. 13. Jay V, Greenberg M. Unusual cerebellar

Intraventricular ganglioglioma: case report

quent intracranial location of gan-glioglioma is the temporal lobe, any location in the central nervous sys-tem may be seen. Nevertheless an exclusively intraventricular location is exceptional. To our knowledge this is the first complete radiological report of a purely intraventricular ganglioglioma. Key words Ganglioglioma ×

Osseous erosion by herniated nucleus pulposus mimicking

et al (1998) MR of spinal cord ganglioglioma. Am J Neuroradiol 19:879 887 7. Tabaddor K, Lamorgese JR (1975) Lumbar epidermoid cyst following single spinal puncture: case report. J Bone Joint Surg Am 57:1168 1169 8. Wakely SL (2006) The posterior vertebral scalloping sign. Radiology 239:607 609 9. Crawford AH, Parikh S, Schorry EK, Von

Radiation Therapy of Cerebellar Gangliogliomas: Case Report

Case Report and Review of the Literature. Author(s): Lalya I , Bellefqih S , Khalil J, Allaoui M, Elkhannoussi B, Hassouni K, Kebdani T, Elgueddari B, Benjaafar N. Abstract. Gangliogliomas are rare neoplasms, histologically defined by the presence of both atypical ganglion cells and neoplastic glial cells. Usually located in the

Case Report Intracranial ganglioglioma A rare case report

neoplasms associated with good prognosis. We report a rare case of intracranial ganglioglioma in a 10 year old boy who underwent surgery and adjuvant radiotherapy. Keywords: Adjuvant radiotherapy, Gangliogliomas, Glial, Ganglion cells, Intracranial neoplasms. Introduction Ganglioglioma is a rare neuroepithelial tumor of