Spontaneous intraventricular hemorrhage from low-grade optic glioma: case report and review of the literature

2011 ◽  
Vol 28 (2) ◽  
pp. 327-330 ◽  
Author(s):  
Jason D. Hill ◽  
Michael S. Rhee ◽  
John R. Edwards ◽  
Matthew C. Hagen ◽  
Daniel H. Fulkerson
2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Gene M. Weinstein ◽  
Knarik Arkun ◽  
James Kryzanski ◽  
Michael Lanfranchi ◽  
Gaurav K. Gupta ◽  
...  

Ependymomas are common spinal lesions, with the vast majority arising in an intramedullary location. Several cases have been described in the literature of ependymomas in an intradural, extramedullary location. The authors present a case of a 56-year-old female who presented with several weeks of lower back pain and weakness. MRI revealed an intradural, extramedullary enhancing mass at L1-L2. The mass was successfully resected surgically. Pathologic evaluation revealed a low grade glioma with components of both ependymoma and pilocytic astrocytoma with MUTYH G382D mutation. Extramedullary ependymomas are very rare tumors. To the authors’ knowledge, this is the first case of ependymoma/astrocytoma collision tumors described in an extramedullary location.


Author(s):  
Masami Kawaharada ◽  
Wataru Katagiri ◽  
Satoshi Maruyama ◽  
Hideyoshi Nishiyama ◽  
Takafumi Hayashi ◽  
...  

2015 ◽  
Vol 7 ◽  
pp. 168-171 ◽  
Author(s):  
Barbara A. Morais ◽  
Djalma F.S. Menendez ◽  
Raphael S.S. Medeiros ◽  
Manoel J. Teixeira ◽  
Guilherme A. Lepski

2018 ◽  
Vol 2018 ◽  
pp. 1-5
Author(s):  
Rauf Melekoglu ◽  
Ebru Celik ◽  
Hasim Kural

Intrauterine transfusion is the most common and successful intrauterine procedure for the treatment of fetal anemia due to red cell alloimmunization. Fetal intracranial hemorrhage is a very rare complication of intrauterine transfusion in patients with Rh(D) alloimmunization and it has been demonstrated only in a few case reports in the literature. Herein, we described a case of grade IV intraventricular hemorrhage that was diagnosed following the first intrauterine transfusion and reviewed the literature about the fetal intracranial hemorrhage that occurred after intrauterine intravascular transfusion procedure.


2012 ◽  
Vol 48 (3) ◽  
pp. 174-180 ◽  
Author(s):  
Venkatesh S. Madhugiri ◽  
Sudheer Kumar Gundamaneni ◽  
Awdhesh Kumar Yadav ◽  
Gopalakrishnan M. Sasidharan ◽  
Kumar V.R. Roopesh

2016 ◽  
Vol 12 (02) ◽  
pp. 97
Author(s):  
Michel Kmeid ◽  
Elie Azar ◽  
Selim Nasser ◽  
Pierre Abi Hanna ◽  
Maya Saroufim ◽  
...  

Background: Invasive laryngeal aspergillosis is an uncommon disorder. The presentation can be misleading, mimicking other laryngeal disorders, specifically laryngeal cancer. The isolated involvement of the larynx is even more unusual making the diagnosis even more challenging. Case report: We describe the case of a 66-year-old man with diabetes who presented with a sore throat, low grade fever, dysphagia, and odynophagia of 3 days duration. He was initially diagnosed as having a supraglottic laryngeal cancer with involvement and paralysis of the left vocal cord. However, further histopathologic examination revealed the presence of an invasive epiglottic aspergillosis with no evidence of malignancy. He was treated with surgical debridement and voriconazole for 3 weeks and responded well to therapy with full recovery. Conclusion: In the presence of laryngeal ulcerative and/or granulomatous lesions, the possibility of invasive fungal laryngitis (aspergillosis specifically), although improbable, should always be kept in mind especially in the presence of predisposing conditions. Starting empiric antifungal therapy is integral when the disease is suspected but therapy is often delayed until pathologic confirmation is obtained. Prognosis is usually poor and will depend on the immune status of the patient.


Sign in / Sign up

Export Citation Format

Share Document