scholarly journals Imaging findings of malignant bilateral carotid body tumors: A case report and review of the literature

2016 ◽  
Vol 11 (4) ◽  
pp. 2457-2462 ◽  
Author(s):  
HAN LV ◽  
XIAOHONG CHEN ◽  
SHUAI ZHOU ◽  
SUPING CUI ◽  
YUNLONG BAI ◽  
...  
1987 ◽  
Vol 5 (4) ◽  
pp. 648-650 ◽  
Author(s):  
Jeffrey DuBois ◽  
William Kelly ◽  
Patrick McMenamin ◽  
G. Andrew Macbeth

1987 ◽  
Vol 5 (4) ◽  
pp. 648-650 ◽  
Author(s):  
Jeffrey DuBois ◽  
William Kelly ◽  
Patrick McMenamin ◽  
G.Andrew Macbeth

2016 ◽  
Vol 4 (2) ◽  
pp. 41-44
Author(s):  
Sadi Kaplan ◽  
Tuğba Avcı ◽  
Çetin Murat Songur

1989 ◽  
Vol 82 (2) ◽  
pp. 265-270
Author(s):  
Kunihiko Chinzei ◽  
Seiji Kishimoto ◽  
Haruo Saito ◽  
Yoichi Katto ◽  
Shunji Takeuchi ◽  
...  

2018 ◽  
pp. e000109
Author(s):  
Ahsan Zil-E-Ali ◽  
Zubair Ahmed ◽  
Amber Ehsan Faquih ◽  
Muhammad Ishaq ◽  
Muhammad Aadil

Background: Carotid body paragangliomas are rare neuroendocrine neoplasms of chromaffin negative glomus cells. This case report explains an atypical case with unusual presentation and treatment. Case Report: A healthy smoker technician by profession was brought to the emergency room (ER) with coprolalia. The general physical exam did not reveal any information. His history revealed unilateral tinnitus and odynophagia leading to a consultation by the neurologist with head imaging. Acoustic neuroma was ruled out and the caregiver was asked to elaborate the events mentioned in the history and a psychiatric examination was done. The personality changes were evaluated by the psychiatrist that showed overlapping of delirium and depression. The patient was further examined by a vascular surgeon. After careful revisiting of the history, examination and indication of tender mass in the neck by the patient's vascular surgeon, the diagnosis of carotid body paraganglioma was made which was followed by surgical resection for treatment. Conclusion: Carotid Body Paragangliomas are very vascular structures and their manipulation in a surgery setting requires expertise. This case presented with personality changes and tinnitus, a very less likely event to occur in a carotid body tumor. The present care report, thus adds on to the literature of carotid body tumors and its presenting symptoms.


2021 ◽  
Vol 20 ◽  
Author(s):  
Mustafa Etli ◽  
Oguz Karahan

Abstract Moyamoya disease is a rare disorder that involves the cerebrovascular system. Usually, it leads to occlusion of the arteries of the cerebral system and causes cerebral circulatory complaints. A 48-year-old female patient was admitted to our clinic with intermittent claudication in both legs. Biphasic and monophasic waveform patterns were detected bilaterally in distal (trifurcation arteries) lower extremities with Doppler sonography. The patient therefore underwent systemic vascular examination. Computed tomography angiography revealed bilateral carotid occlusion at the level of supraclinoid segments, and opacifications were detected at the distal segments of the bilateral anterior cerebellar and middle cerebellar arteries. The patient was diagnosed with moyamoya disease, and anticoagulant treatment was started. In conclusion, most previous reports have presented the cerebrovascular involvement of moyamoya disease. However, this disease can involve different peripheral vascular systems and careful and systemic vascular examination is necessary for an exact diagnosis.


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