scholarly journals Burkitt lymphoma presenting rapid progression from unilateral to bilateral cavernous sinus syndrome as the initial symptom

2014 ◽  
Vol 2 (6) ◽  
pp. 204-206 ◽  
Author(s):  
Yuji Tanaka ◽  
Yui Takagi ◽  
Senji Kasahara ◽  
Hideko Goto ◽  
Takeshi Takahashi ◽  
...  
Author(s):  
A. Aramburu-González ◽  
P. Rivera-Pérez De Rada ◽  
L. Antón-Méndez ◽  
M. Cisneros-Carpio ◽  
O. Arce-Fernández

Author(s):  
Weronika Jakubowska ◽  
Sarah Chorfi ◽  
Caroline Bélanger ◽  
Jean-Claude Décarie ◽  
Luis H. Ospina

Medicine ◽  
2017 ◽  
Vol 96 (46) ◽  
pp. e8687
Author(s):  
Florette Reyneke ◽  
Neo Mokgoro ◽  
Mariza Vorster ◽  
Mike Sathekge

Author(s):  
Enzo Emanuelli ◽  
Maria Baldovin ◽  
Claudia Zanotti ◽  
Sara Munari ◽  
Luca Denaro ◽  
...  

AbstractWhile the so-called pseudoaneurysms can result from arterial injury during trans-sphenoidal surgery or after a trauma, spontaneous aneurysms of cavernous–internal carotid artery (CICA) are rare. Symptoms vary and the differential diagnosis with other, more frequent, sellar lesions is difficult. We describe three cases of misdiagnosed CICA spontaneous aneurysm. In two cases the onset was with neuro-ophthalmological manifestations, classifiable as “cavernous sinus syndrome.” The emergency computed tomography scan did not show CICA aneurysm and the diagnosis was made by surgical exploration. The third patient came to our attention with a sudden severe unilateral epistaxis; endonasal surgery revealed also in this case a CICA aneurysm, eroding the wall and protruding into the sphenoidal sinus. When the onset was with a cavernous sinus syndrome, misdiagnosis exposed two patients to potential serious risk of bleeding, while the patient with epistaxis was treated with embolization, using coils and two balloons. Intracavernous nontraumatic aneurysms are both a diagnostic and therapeutic challenge, because of their heterogeneous onset and risk of rupture, potentially lethal. Intracavernous aneurysms can be managed with radiological follow-up, if asymptomatic or clinically stable, or can be surgically treated with endovascular or microsurgical techniques.


2021 ◽  
pp. 329-333
Author(s):  
Kanako Kurihara ◽  
Jun Tsugawa ◽  
Shinji Ouma ◽  
Toshiyasu Ogata ◽  
Mikiko Aoki ◽  
...  

A 66-year-old woman with a history of bronchial asthma had shortness of breath and fatigue upon mild exercise. She was diagnosed as congestive heart failure. A blood test showed eosinophilia without the presence of anti-neutrophil cytoplasmic antibody (ANCA), and a myocardial biopsy specimen revealed eosinophilic infiltration in the myocardium. Eosinophilia was improved when she was administered short-term methylprednisolone. After that, she had numbness and pain in her lower limbs with re-elevation of eosinophils. She had dysesthesia and hypalgesia in the distal part of the limbs. Sural nerve biopsy revealed axonal degeneration and thickness of the arterial wall, indicating a diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA). Two courses of steroid pulse therapy were performed, resulting in marked improvement of her sensory symptoms. ANCA-negative EGPA might be associated with myocarditis and peripheral neuropathy. A sufficient immunotherapy should have been considered to prevent rapid progression.


2008 ◽  
Vol 15 (10) ◽  
pp. 1148-1151 ◽  
Author(s):  
Shu-Mei Chen ◽  
Chen-Nen Chang ◽  
Kuo-Chen Wei ◽  
Shih-Ming Jung ◽  
Chi-Cheng Chuang

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