scholarly journals Fatty falx cerebri

2021 ◽  
Author(s):  
Naqibullah Foladi
Keyword(s):  
Falx Cerebri

Verkalkung der Falx cerebri

HNO ◽  
2005 ◽  
Vol 53 (8) ◽  
pp. 701-706 ◽  
Author(s):  
J. T. Lambrecht ◽  
S. Stübinger ◽  
B. Siewert ◽  
F. Härle
Keyword(s):  
Falx Cerebri

scholarly journals Ossification of the falx cerebri: A review

2017 ◽  
Vol 7 ◽  
pp. 20-22 ◽  
Author(s):  
Andre Granger ◽  
Seunghwan Kim ◽  
Theofanis Kollias ◽  
Tina Rajnauth
Keyword(s):  
Falx Cerebri

scholarly journals Falx Cerebri Giant Chondroma ‒ Case Report

2017 ◽  
Vol 08 (04) ◽  
Author(s):  
Mugurel Petrinel Radoi ◽  
Ram Vakilnejad ◽  
Lidia Gheorghitescu ◽  
Florin Stefanescu
Keyword(s):  
Case Report ◽  
Falx Cerebri

scholarly journals Idiopathic Hypertrophic Pachymeningitis Manifesting with Frontal Brain Edema

2001 ◽  
Vol 19 (3) ◽  
pp. 491-495
Author(s):  
Mário Emílio Teixeira Dourado Júnior ◽  
Ricardo Humberto de Miranda Félix ◽  
Marcos Dias Leão
Keyword(s):  
Dura Mater ◽  
Histopathological Study ◽  
Hypertrophic Pachymeningitis ◽  
Falx Cerebri ◽  
Additional Information ◽  
Frontal Brain ◽  
History Of ◽  
Cerebral Parenchyma ◽  
Magnetic Resonance Imaging Mri ◽  
The Brain

Introduction. Hypertrophic pachymeningitis (HP) is a rare inflammatory disease that results in thickening of the dura mater. Atypically, it can progress to include the involvement of the cerebral parenchyma. Method. In this paper, we report the rare case of a 31-year-old man with a three-week history of headaches, seizures, impairments of cognitive function, and changes in behavior and mood. Magnetic resonance imaging (MRI) of the brain showed a thickening and an abnormal enhancement of the dura mater over the falx cerebri with extensions into the adjacent cranial base and with brain edemas in the frontal lobes. Histopathological study of meningeal and brain biopsies showed an inflammatory process that was compatible with HP. The results of an extensive laboratory investigation were unremarkable and did not provide additional information on the cause of the meningeal disease. The patient exhibited relapses despite immunosuppressive therapy. Conclusion. This case shows the challenges associated with the management of the disease and the importance of early diagnosis to avoid worsening of the condition and cerebral damage.

Intracranial xanthogranuloma of the dura in Hand-Schüller-Christian disease

1993 ◽  
Vol 78 (2) ◽  
pp. 297-300 ◽  
Author(s):  
Zain Alabedeen B. Jamjoom ◽  
Vinita Raina ◽  
Abdulfattah Al-Jamali ◽  
Abdulhakim B. Jamjoom ◽  
Basim Yacub ◽  
...  
Keyword(s):  
Intracranial Pressure ◽  
Clinical Features ◽  
Obstructive Hydrocephalus ◽  
Relevant Literature ◽  
Increased Intracranial Pressure ◽  
Falx Cerebri ◽  
Content Type ◽  
Tentorium Cerebelli ◽  
Ultrastructural Studies ◽  
Fine Print

✓ The authors describe a 37-year-old man with the classic clinical features of Hand-Schüller-Christian disease. He presented with symptoms of increased intracranial pressure due to obstructive hydrocephalus secondary to a huge xanthogranuloma involving falx cerebri and tentorium cerebelli. Immunohistochemical and ultrastructural studies failed to demonstrate Langerhans histiocytes, however. The implication of this finding is discussed in light of the recent relevant literature.

Ossification of falx cerebri: a case report

2018 ◽  
Vol 67 ◽  
pp. S16
Author(s):  
M. Angom ◽  
D. Bandopadhay ◽  
S. Kumar
Keyword(s):  
Case Report ◽  
Falx Cerebri

scholarly journals Giant pericallosal artery aneurysm – Literature review and report of a rare case

2013 ◽  
Vol 32 (03) ◽  
pp. 195-199
Author(s):  
José Fernando Guedes Corrêa ◽  
Ari Boulanger Sucussel Junior ◽  
Rogério Martins Pires Amorim ◽  
Lucas Santos Loiola ◽  
Maristella Reis ◽  
...  
Keyword(s):  
Surgical Treatment ◽  
Cerebral Arteries ◽  
Clinical Status ◽  
Artery Aneurysm ◽  
Mass Effect ◽  
Imaging Studies ◽  
Falx Cerebri ◽  
Aneurysm Neck ◽  
Pericallosal Artery ◽  
Medial Surfaces

AbstractGiant pericallosal artery aneurysms are extremely rare. Aneurismatic lesions involving this artery are usually small, tend to early bleeding and might be associated with other lesions. Differential diagnosis of giant aneurysms are not easy and includes tumoral, infectious and vascular mass effect lesions. We report a case of a giant and partially thrombosed left pericallosal artery aneurysm. A 58-year-old man, presented with progressive headaches, seizures and speech alterations initially misdiagnosed as a falx cerebri meningioma. As clinical status continue to worsen, magnetic resonance imaging and digital cerebral angiography were performed and a vascular etiology was considered. The patient was then referred to our hospital for surgical treatment. The peculiarity of this case concerns the difficulty of surgical treatment once the surgeon was not able to obtain control of the afferent artery and the aneurysm neck could not be visualized. Also, the aneurysm adhered to the medial surfaces of the frontal lobes and covered the anterior cerebral arteries. Treatment by means of microsurgical thrombectomy, clipping and resection of the lesion was successfully performed. Microsurgical treatment may provide good results when carefully planned with the help of imaging studies of the lesion. It is essential to keep in mind that flexible approach is of great importance when dealing with giant aneurysmatic lesions of pericallosal artery due to its variety of intraoperative presentation.

Fenestrated Falx Cerebri and Additional Sinuses in the Tentorium Cerebelli

2020 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Satheesha B. Nayak ◽  
Soumya K. Vasudeva
Keyword(s):  
Falx Cerebri ◽  
Tentorium Cerebelli

scholarly journals Intracranial solitary chondroma

1984 ◽  
Vol 61 (2) ◽  
pp. 399-401 ◽  
Author(s):  
Tunçalp Özgen ◽  
M. Necmettin Pamir ◽  
Nejat Akalan ◽  
Vural Bertan ◽  
Behsan Önol
Keyword(s):  
Computerized Tomography ◽  
Pathological Condition ◽  
Diagnostic Value ◽  
Falx Cerebri ◽  
Content Type ◽  
Intracranial Chondroma ◽  
Fine Print

✓ A patient is described who had a solitary left frontal intracranial chondroma originating from the falx cerebri. The tumor was totally removed. The diagnostic value of computerized tomography and the surgical findings in this rare pathological condition are discussed.

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