Invasive Epiglottic Aspergillosis Mimicking Supraglottic Laryngeal Carcinoma—A Case Report and Review of the Literature

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.

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.


2011 ◽  
Vol 28 (2) ◽  
pp. 327-330 ◽  
Author(s):  
Jason D. Hill ◽  
Michael S. Rhee ◽  
John R. Edwards ◽  
Matthew C. Hagen ◽  
Daniel H. Fulkerson

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

1997 ◽  
Vol 47 (4) ◽  
pp. 264-267 ◽  
Author(s):  
Soichiro Shizawa ◽  
Hironobu Sasano ◽  
Takashi Suzuki ◽  
Hirhi Ishii ◽  
Tetsutaro Takeda ◽  
...  

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