Benign Osteoblastoma - An Unusual Rare Clinical Presentation

2012 ◽  
Vol 3 (1) ◽  
pp. 21-24 ◽  
Author(s):  
Chandramani B. More ◽  
Sunanda K. Das ◽  
Khushbu S. Bhavsar ◽  
Mansi N. Tailor
2019 ◽  
Vol 36 (1) ◽  
pp. 107-111
Author(s):  
Dhanya Mary Sam ◽  
Sreeja P. Kumar ◽  
Beena Varma ◽  
Anju P. David ◽  
Rakesh Suresh

1995 ◽  
Vol 109 (6) ◽  
pp. 565-568 ◽  
Author(s):  
Ahmad Khashaba ◽  
Giuseppe De Donato ◽  
Gabriele Vassallo ◽  
Mauro Landolfi ◽  
Alessandra Russo ◽  
...  

AbstractOsteoblastoma is a benign bone lesion that mainly affects the long bones and rarely the temporal bones. Very few cases have been reported in the literature. This paper reviews the literature, discusses the differential diagnosis, clinical presentation, and CT scan findings of such a condition and details our experience with a young patient who had a temporal bone (mastoid process) osteoblastoma.


Author(s):  
Line Buhl ◽  
David Muirhead

There are four lysosomal diseases of which the neuronal ceroid lipofuscinosis is the rarest. The clinical presentation and their characteric abnormal ultrastructure subdivide them into four types. These are known as the Infantile form (Santavuori-Haltia), Late infantile form (Jansky-Bielschowsky), Juvenile form (Batten-Spielmeyer-Voght) and the Adult form (Kuph's).An 8 year old Omani girl presented wth myclonic jerks since the age of 4 years, with progressive encephalopathy, mental retardation, ataxia and loss of vision. An ophthalmoscopy was performed followed by rectal suction biopsies (fig. 1). A previous sibling had died of an undiagnosed neurological disorder with a similar clinical picture.


2012 ◽  
Vol 21 (3) ◽  
pp. 75-84
Author(s):  
Venkata Vijaya K. Dalai ◽  
Jason E. Childress ◽  
Paul E Schulz

Dementia is a major public health concern that afflicts an estimated 24.3 million people worldwide. Great strides are being made in order to better diagnose, prevent, and treat these disorders. Dementia is associated with multiple complications, some of which can be life-threatening, such as dysphagia. There is great variability between dementias in terms of when dysphagia and other swallowing disorders occur. In order to prepare the reader for the other articles in this publication discussing swallowing issues in depth, the authors of this article will provide a brief overview of the prevalence, risk factors, pathogenesis, clinical presentation, diagnosis, current treatment options, and implications for eating for the common forms of neurodegenerative dementias.


2001 ◽  
Vol 71 (6) ◽  
pp. 341-344
Author(s):  
Johanna Rose ◽  
Ian Civil ◽  
Timothy Koelmeyer ◽  
David Haydock ◽  
Dave Adams

2016 ◽  
Vol 22 ◽  
pp. 21
Author(s):  
Sri Nagesh. V ◽  
Y. Muralidhar Reddy ◽  
Prajnya Ranganath ◽  
Vikrant Reddy

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