Jugular foramen schwannoma presenting with glossopharyngeal neuralgia syncope syndrome

2010 ◽  
Vol 124 (12) ◽  
pp. 1305-1308 ◽  
Author(s):  
Y Saman ◽  
D Whitehead ◽  
M Gleeson

AbstractIntroduction:Jugular foramen schwannomas are rare skull base tumours which typically have a variable clinical presentation. Glossopharyngeal syncope syndrome is an unusual clinical presentation; in the following case report, it was the sole presentation of an extracranial jugular foramen tumour.Methods:The presentation of a patient with glossopharyngeal neuralgia syncope syndrome is reviewed and the pathophysiology, clinical features and treatment discussed.Results:A 45-year-old woman presented with unilateral throat pain, bradycardia and hypotension leading to episodes of impaired consciousness when lying on her left side or turning her head to the left. Imaging detected a left-sided extracranial jugular foramen schwannoma. The tumour was excised, and the patient had no more syncopal attacks.Conclusion:Glossopharyngeal neuralgia syncope syndrome can be the sole presentation of a jugular foramen schwannoma. Although this syndrome may be treated with anti-dysrhythmic drugs, cardiac pacing or nerve section, in the presented patient excision of the jugular foramen schwannoma was successful in preventing further episodes of syncope.

2012 ◽  
Vol 16 (4) ◽  
pp. 288-290 ◽  
Author(s):  
Ashley O'toole ◽  
Maureen O'malley

Background: Keratoderma is a group of conditions characterized by hyperkeratosis affecting the skin on the soles of the feet and palms of the hands bilaterally. The classification of keratodermas depends on whether it is inherited or acquired and on its clinical features, including diffuse or focal involvement of the skin and the morphology of lesions present. Case Report: We describe the rare case of a 54-year-old female who presented with a nearly 40-year history of punctate keratoderma on her right palm and sole. History taking revealed that her biologic son also has unilateral left-sided keratoderma. The clinical presentation of unilateral keratoderma has been reported only four times in the literature.


1970 ◽  
Vol 14 (2) ◽  
pp. 248-252 ◽  
Author(s):  
Ki Won Lee ◽  
Young Joon Choi ◽  
Hyung Sun Ahn ◽  
Chung Hwan Kim ◽  
Jae Kwang Hwang ◽  
...  

PURPOSE: We report a case of chronic recurrent multifocal osteomyelitis of the shoulder.MATERIALS AND METHODS: A 16 year-old male who had suffered from chronic recurrent multifocal osteomyelitis of the shoulder was diagnosed by clinical features and biopsy and was treated with arthroscopic debridement and Naproxen.RESULTS: Symptoms was subsided without relapse during 16 months follow up.CONCLUSION: Chronic recurrent multifocal osteomyelitis is rare disease and it can be misdiagnosis because of its rarity and non-specific clinical presentation. This is a report of a case of chronic recurrent multifocal osteomyelitis of the shoulder in 16 years man.


2008 ◽  
Vol 05 (02) ◽  
pp. 109-111 ◽  
Author(s):  
SGS Datta

AbstractBilateral vertex extra dural hematomas (EDH) are a rare form of extra dural hematomas with many unique features. We report one such case of bilateral vertex extra dural hematoma. A young house wife had a fall in the bathroom and sustained head injury. She showed clinical features of progressive raised intra cranial pressure. Neuroimaging revealed bilateral vertex EDH. The larger left sided hematoma was evacuated surgically while the smaller right sided hematoma was managed non operatively, with excellent outcome. This case report presents this rare case and briefly reviews the literature. Vertex EDH has a special uniqueness as to their etiopathology, clinical presentation, diagnosis & management principles.


Neurosurgery ◽  
1987 ◽  
Vol 21 (6) ◽  
pp. 916-919 ◽  
Author(s):  
K. Reddy ◽  
D.E. Hobson ◽  
A. Gomori ◽  
G.R. Sutherland

Abstract Glossopharyngeal neuralgia is an uncommon craniofacial pain syndrome. An association with syncope is even less common. We report a case illustrating that the glossopharyngeal neuralgia-syncope syndrome can occur without pain in the sensory distribution of the glossopharyngeal nerve and that it can have similar consequences. We suggest that permanent cardiac pacing alone may be a viable option in the initial management of such cases.


2017 ◽  
Vol 4 (4) ◽  
pp. 1444
Author(s):  
Dileep Kumar Singh Rathor ◽  
Narender Singh Jhajhria ◽  
V. K. Gupta

Primary intracardiac tumors are rare and approximately 50% are myxomas. Majority of myxomas are located in left atrium. Most of myxomas are attached to inter-atrial septum and have variable clinical presentation depending on size, location and mobility of the tumor. We report a case of large myxoma in the right atrium with atypical clinical presentation and location for this type of tumor.


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Matthias Sperl ◽  
Michael Novak ◽  
Daniela Sperl ◽  
Martin Svehlik ◽  
Georg Singer ◽  
...  

The incidence of osteomyelitis constantly declines. While the disease most commonly affects the long bones, involvement of the patella is rarely seen. Due to this rarity and the variable clinical presentation, diagnosis is often delayed. The present case report describes a 10-year-old female patient with a delayed diagnosis of patella osteomyelitis. The diagnostic procedures and the treatment regimen are described. Additionally, a detailed literature review of the available publications reporting osteomyelitis of the patella in children is presented.


2017 ◽  
Vol 8 (2) ◽  
pp. 89-92
Author(s):  
Ashok Bhansali ◽  
Setu Mathur ◽  
Gunjan Bhansali ◽  
Anuroopa Kishan

ABSTRACT Palmoplantar keratodermas (PPKs) comprise a heterogeneous group of keratinization disorders with hyperkeratotic thickening of palms and soles. The PPKs are distinguished by their mode of inheritance and by the presence of certain associated clinical features. Periodontitis was reported in association with more than one syndrome characterized by PPK. Knowledge about heterogeneous groups of acquired or hereditary PPK is important, leading to an appropriate diagnosis and corrective therapies in the future. This case report aims at critically reviewing the literature concerned with PPK and its clinical presentation, in addition to other syndromes manifested along with periodontitis. How to cite this article Bhansali A, Kishan A, Mathur S, Bhansali G. Palmoplantar Keratoderma with Periodontitis. J Health Sci Res 2017;8(2):89-92.


2014 ◽  
Vol 75 (S 01) ◽  
Author(s):  
Óscar Feo Lee ◽  
Juan Carlos Acevedo G. ◽  
Roberto Díaz O ◽  
Miguel Berbeo C. ◽  
Óscar Zorro G. ◽  
...  

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