scholarly journals A rare case of intracerebral hemorrhage due to arteriovenous malformation located at petrous portion of the temporal bone.

2012 ◽  
Author(s):  
Emre Cemal Gokce ◽  
Berker Cemil ◽  
Ismail Kirbas ◽  
Alper Bozkurt ◽  
Bulent Erdogan
Keyword(s):  
Intracerebral Hemorrhage ◽  
Arteriovenous Malformation ◽  
Temporal Bone ◽  
Rare Case ◽  
Petrous Portion

scholarly journals Aneurysmal Bone Cyst in the Temporal Bone and Complete Resection with Preoperative Embolization

2014 ◽  
Vol 20 (5) ◽  
pp. 609-613 ◽  
Author(s):  
Byoung Je Kim ◽  
Eun Ju Lee ◽  
Hyuk Won Chang ◽  
Hae Ra Jung ◽  
Ealmaan Kim ◽  
...  
Keyword(s):  
Temporal Bone ◽  
Rare Case ◽  
Bone Cyst ◽  
Complete Removal ◽  
Complete Resection ◽  
Preoperative Embolization ◽  
Aneurysmal Bone Cysts ◽  
Technical Details ◽  
Petrous Portion ◽  
Good Treatment Option

We describe a rare case of aneurysmal bone cysts (ABCs) that occurred in the petrous portion of the temporal bone. The ABCs were treated with preoperative embolization and complete removal of the mass from the adjacent tissue. The technical details suggest that preoperative embolization is a good treatment option for ABCs.

scholarly journals Endolymphatic Sac Tumor: A Rare Case

2020 ◽  
pp. 1-4
Author(s):  
Amal Algarni ◽  
Amal Algarni ◽  
Yaser Orz ◽  
Sofia Muzzafar ◽  
Wafa Alshakweer
Keyword(s):  
Hearing Loss ◽  
Temporal Bone ◽  
Rare Case ◽  
Disease Patient ◽  
Endolymphatic Sac ◽  
Endolymphatic Sac Tumor ◽  
Von Hippel Lindau ◽  
Von Hippel Lindau Disease ◽  
Petrous Portion ◽  
Vhl Disease

Endolymphatic sac tumor is rare, locally aggressive and non-metastasizing neoplasm arising from the endolymphatic sac of the petrous portion of the temporal bone. Most occur in adult and present with ipsilateral hearing loss. They can be sporadic or associated with Von-Hippel-Lindau disease. Patient with endolymphatic sac tumor should be screened for VHL disease. We report a case of 52-year-old female with dizziness and headache. Histopathology was consistent with typical features of endolymphatic sac tumor. This was confirmed by cytokeratin and EMA positivity and TTF-1 negativity. This case is presented for its rarity with only few cases reported.

Diagnostic and Therapeutic Tricks in a Rare Case of Pediatric Ileal Congenital Arteriovenous Malformation

2010 ◽  
Vol 51 (1) ◽  
pp. 90-92 ◽  
Author(s):  
Massimiliano Silveri ◽  
Piergiorgio Falappa ◽  
Emanuele Casciani ◽  
Gianluigi Natali ◽  
Massimo Rivosecchi
Keyword(s):  
Arteriovenous Malformation ◽  
Rare Case ◽  
Congenital Arteriovenous Malformation

Extracranial meningioma presenting as a tumour of the external auditory meatus: a case report

1997 ◽  
Vol 111 (2) ◽  
pp. 148-151 ◽  
Author(s):  
Reiko Tsunoda ◽  
Takashi Fukaya
Keyword(s):  
Temporal Bone ◽  
Rare Case ◽  
External Auditory Meatus ◽  
Middle Cranial Fossa ◽  
External Meatus ◽  
Cranial Fossa ◽  
Magnetic Resonance Imaging Mri ◽  
Extracranial Meningioma ◽  
Operative Findings ◽  
Intradural Space

AbstractA rare case of extracranial meningioma presenting as a tumour of the external auditory meatus is reported. Biopsy indicated a diagnosis of meningioma, but the radiological appearance was unusual. For example, computed tomography (CT) scans showed an unenhanced tumour mainly located in the squamous part of the temporal bone which expanded into the external meatus destroying the temporal bone. Magnetic resonance imaging (MRI) revealed that the tumour did not extend into the intradural space.This meningioma, had an obvious tendency for extracranial development. According to the operative findings, the tumour arose from the middle cranial fossa dura and extended through the air cells of the temporal bone into the external meatus, instead of growing intracranially.Secondary extracranial meningiomas of the temporal bone usually have a large intracranial component and cause neurological symptoms. However, this was a very rare case of a small meningioma causing no symptoms except for conductive hearing loss.

scholarly journals Postoperative ‘STEMI’ in Intracerebral Hemorrhage due to Arteriovenous Malformation: A Case Report and Review of Literature

2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Ravinder Datt Bhanot ◽  
Jasleen Kaur ◽  
Shitiz Sriwastawa ◽  
Kendall Bell ◽  
Kushak Suchdev
Keyword(s):  
Myocardial Infarction ◽  
Intracerebral Hemorrhage ◽  
Arteriovenous Malformation ◽  
Cardiac Biomarkers ◽  
Review Of Literature ◽  
Fibrinolytic Agents ◽  
Intraparenchymal Hemorrhage ◽  
Ecg Changes ◽  
St Segment ◽  
Electrocardiogram Ecg

Electrocardiogram (ECG) changes suggestive of cardiac ischemia are frequently demonstrated in patients with ischemic stroke and subarachnoid hemorrhage. However, little is known of such changes particularly acute ST segment myocardial infarction (STEMI) in patients with intracerebral hemorrhage (ICH), especially after neurosurgery. We present a patient with intraparenchymal hemorrhage due to cerebral arteriovenous malformation (AVM) who exhibited acute STEMI after neurosurgery. Serial cardiac biomarkers and echocardiograms were performed which did not reveal any evidence of acute myocardial infarction. The patient was managed conservatively from cardiac stand point with no employment of anticoagulants, antiplatelet therapy, fibrinolytic agents, or angioplasty and recovered well with minimal neurological deficit. This case highlights that diffuse cardiac ischemic signs on the ECG can occur in the setting of an ICH after neurosurgery, potentially posing a difficult diagnostic and management conundrum.

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