scholarly journals Fourth ventricular ependymoma with a distant intraventricular metastasis: Report of a rare case

2013 ◽  
Vol 04 (S 01) ◽  
pp. S121-S124 ◽  
Author(s):  
Sudheer Ambekar ◽  
Manish Ranjan ◽  
Sampath Somanna ◽  
Chandrajit Prasad ◽  
Vani Santosh
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Primary Tumor ◽  
Rare Case ◽  
Age Group ◽  
Anaplastic Ependymoma ◽  
Rare Presentation ◽  
Adult Age ◽  
The Central Nervous System

ABSTRACTEpendymoma is one of the uncommon tumors of the central nervous system (CNS) in the adult age group. These tumors have a distinct propensity for metastasis, both within and outside the CNS. However, dissemination at the time of first presentation and retrograde dissemination of the tumor is rare. We report the case of a patient with fourth ventricular anaplastic ependymoma who presented with left lateral ventricular metastasis which was anatomically different from the primary tumor. We describe the clinic‑pathological detail of the patient and discuss the probable pathophysiological basis for this rare presentation and its significance in management of the patient.

scholarly journals Schwannoma of the arythenoid

2013 ◽  
Vol 11 (2) ◽  
pp. 224-226 ◽  
Author(s):  
Carlos Eduardo Molinari Nardi ◽  
Alexandre Wakil Burzichelli ◽  
Elio Gilberto Pfuetzenreiter ◽  
Rogerio Aparecido Dedivitis
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Schwann Cells ◽  
Rare Case ◽  
Nerve Fibers ◽  
Endoscopic Procedure ◽  
The Central Nervous System

Schwannoma is a benign encapsulated tumor that originates from the Schwann cells lining nerve fibers outside the central nervous system. We report a rare case of schwannoma that arose from the left arythenoid cartilage The patient underwent excision of the mass through microlaryngeal endoscopic procedure. No recurrence was observed during follow-up.

scholarly journals A Rare Case of Pericallosal Lipoma Associated with Bilaterally Symmetrical Lateral Ventricular Choroid Plexus Lipomas without Corpus Callosal Anomalies

2013 ◽  
Vol 3 ◽  
pp. 69 ◽  
Author(s):  
Parag Suresh Mahajan ◽  
Nawal M. Al Moosawi ◽  
Islam Ali Hasan
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Brain Tumors ◽  
Corpus Callosum ◽  
Choroid Plexus ◽  
Rare Case ◽  
Rare Presentation ◽  
Pericallosal Lipoma ◽  
Central Nervous System Anomalies

Lipomas constitute less than 5% of primary brain tumors. Pericallosal lipomas (PCLp) constitute almost half of all intracranial lipomas. Corpus callosal anomalies commonly occur in cases with PCLps. Although PCLp is often described as corpus callosal lipoma, it is most often pericallosal in location. PCLps may have calcification in the periphery and may continue into lateral ventricles, which is a very rare presentation. We observed a case of PCLp with peripheral calcifications associated with PCLp continuing as bilaterally symmetrical lateral ventricular choroid plexus lipomas (CPLp) without any corpus callosal or other central nervous system anomalies, and as this is not been previously reported, we are presenting it. The appearance of PCLp in this case does not correspond to the descriptions of any of the existing morphological types (anterior and posterior) of classification of PCLps; it is rather mixed, where PCLp occupies both anterior and posterior locations around the corpus callosum.

scholarly journals A Rare Case of Cysticercosis Involving the Whole Spinal Canal

2021 ◽  
Author(s):  
Xiaoyan Zheng ◽  
Fei Wang ◽  
Lei Wang ◽  
Xiaoli Li ◽  
Jingjing Li ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Central Nervous System ◽  
Nervous System ◽  
Spinal Canal ◽  
Rare Case ◽  
Parasitic Disease ◽  
Epidemiological Investigation ◽  
Case Presentation ◽  
Life Threatening ◽  
The Central Nervous System

Abstract Background Cysticercosis is the commonest parasitic disease to affect the central nervous system (CNS). However, cysticercosis affecting the spine is extremely rare. We reported a rare case of cysticercosis involving the whole spinal canal in China. Case Presentation A rare case of cysticercosis involving the entire spinal cord, in a 52-year-old Chinese man, was detected in 2021. Epidemiological investigation, clinical and etiological examination was performed. Conclusion Since spinal cysticercosis is a rare but potentially life-threatening disease, clinicians should always consider the differential diagnosis of space-occupying lesions.

Diagnostic Difficulties in Primary Pauci-Melanotic Leptomeningeal Melanomatosis

2018 ◽  
Vol 80 (1-2) ◽  
pp. 68-70
Author(s):  
Ewa Koziorowska-Gawron ◽  
Maciej Kaczorowski ◽  
Joanna Bladowska ◽  
Sławomir Budrewicz ◽  
Magdalena Koszewicz ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Malignant Melanoma ◽  
Rare Case ◽  
Diagnostic Procedures ◽  
Postmortem Examination ◽  
Primary Malignant Melanoma ◽  
Diagnostic Difficulties ◽  
The Central Nervous System

We present a rare case of primary malignant melanoma of the central nervous system. We underline the difficulties we faced during diagnostic procedures. Finally, postmortem examination revealed the diagnosis of primary pauci-­melanotic leptomeningeal melanomatosis.

scholarly journals A STUDY ON A CASE OF SPINAL NEUROCYSTICERCOSIS: A RARE CASE REPORT

2021 ◽  
pp. 44-45
Author(s):  
Piyush Modi ◽  
Rajeev Kumar Singh ◽  
K.S Shahi ◽  
Prateek Shakya
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Case Report ◽  
Rare Case ◽  
Parasitic Infection ◽  
Review Of Literature ◽  
Rare Case Report ◽  
The Central Nervous System

Neurocysticercosis is the most common parasitic infection of the central nervous system worldwide. However , cysticercosis affecting the spine is considered extremely rare. We report one case of spinal cysticercosis with review of literature.

scholarly journals A Rare Case of Spontaneous Remission and Relapse of a Primary Central Nervous System Lymphoma

2018 ◽  
Vol 31 (12) ◽  
pp. 777 ◽  
Author(s):  
Rui Ramos ◽  
João Soares Fernandes ◽  
Marta Almeida ◽  
Rui Almeida
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Rare Case ◽  
Central Nervous System Lymphoma ◽  
Brain Biopsy ◽  
B Cell Lymphoma ◽  
Spontaneous Remission ◽  
Neurological Deficits ◽  
Pubmed Search ◽  
The Central Nervous System

Primary central nervous system lymphoma remission after steroid treatment is a well-known phenomenon, but remission without any type of treatment is extremely rare. We present a rare case of spontaneous remission of a diffuse large B-cell lymphoma of the central nervous system as well as its subsequent reappearance in another location. The atypical presentation misled the neurosurgeons and neurologists, delaying diagnosis and treatment. The patient underwent brain biopsy after the relapse and started radiotherapy and chemotherapy with cytarabine + methotrexate + rituximab. As of 32 months after the diagnosis, the patient remained asymptomatic, with no focal neurological deficits and the disease in complete remission. A PubMed search of the literature up to June 2017 regarding spontaneous remission central nervous system lymphoma was also carried out.

Primary malignant lymphoma of the central nervous system

1986 ◽  
Vol 65 (5) ◽  
pp. 600-607 ◽  
Author(s):  
Kevin Murray ◽  
Larry Kun ◽  
James Cox
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Malignant Lymphoma ◽  
Primary Tumor ◽  
Craniospinal Irradiation ◽  
Late Relapse ◽  
Prior History ◽  
Content Type ◽  
The Central Nervous System ◽  
Fine Print

✓ Eleven patients with primary malignant lymphoma of the central nervous system (CNS) were treated at the Medical College of Wisconsin Affiliated Hospitals between 1964 and 1984. Three patients had a prior history of immunosuppressive therapy following renal transplantation. All patients had biopsy-proven disease and 10 of the 11 were treated with external radiation therapy. The doses to the primary tumor ranged from 34 to 59.4 Gray (Gy). Actuarial (life-table) survival rate was 82% at 1 year and 43% at 3 years. No recurrence was seen after 13 months. Eighty-six reports totaling 693 cases of primary malignant lymphoma of the CNS were found in the literature. Of these, 308 cases were treated with a combination of surgery and irradiation. Overall survival at 5 years for those patients who received more than 50 Gy compared with less than 50 Gy to the primary tumor was 42.3% versus 12.8% (p < 0.05). Twenty-one patients survived longer than 5 years. Late relapse was notable, with 10 (47.6%) of 21 tumors recurring between 5 and 12.5 years after diagnosis. Based on this review, a minimum of 50 Gy radiation to the primary tumor is recommended. While no statement regarding the efficacy of craniospinal irradiation or chemotherapy can be made in view of the small numbers, the use of craniospinal irradiation and/or systemic chemotherapy should be considered for future trials.

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