Glomus tumour: A review of clinical presentation and treatment

2020 ◽  
Vol 10 (2) ◽  
pp. 52
Author(s):  
Ibad Sha ◽  
Ajin Edwin ◽  
Namitha Shah ◽  
Roshna Cini
2012 ◽  
Vol 3 (2) ◽  
pp. 37-38
Author(s):  
Sharmin Ferdousi ◽  
SM Badruddoza

Paraganglioma or glomus tumour are named according to their origin. Jugulotympanic  paragangliomas (JTP) originates in the middle ear. There are several diagnostic pitfalls of this tumour. We now report a rare case of JTP in a 47 years old female. Pre-operative diagnosis of this case was chronic suppurative otitis media, Per-operatively it revealed an irregular     somewhat polypoid mass. On histologic examination the mass composed of nests of round to oval cells surrounded by delicate vascular septae and the diagnosis was JTP. Because JTPs are rare tumour and have variable clinical presentation & different histologic findings they are easy to misdiagnose. However this case report may help to generate awareness and to avoid misinterpretation of JTPs.   DOI: http://dx.doi.org/10.3329/akmmcj.v3i2.11693   AKMMC J 2012: 3(2): 37-38  


2016 ◽  
Vol 8 (3) ◽  
pp. 197-198 ◽  
Author(s):  
Jessica Lunn ◽  
Jeremy Stanton ◽  
Anand Arya

Glomus tumours of the elbow remain a challenge to diagnose correctly and efficiently. We present a case of a glomus tumour as a complication of elbow surgery. This has not been described previously. This case highlights the possibility of injury as a causative factor in these tumours and the difficulty in differentiating them from postoperative neuromas by clinical presentation and ultrasound imaging alone.


1991 ◽  
Vol 105 (11) ◽  
pp. 950-953 ◽  
Author(s):  
A. W. Forrest ◽  
J. J. Turner ◽  
P. A. Fagan

AbstractA rare middle ear tumour is reported. The clinical presentation was similar to that of a glomus tumour but the pathology that of an aggressive papillary middle ear tumour. This is a recently recognized subgroup of middle ear glandular tumours. Clinical findings, imaging, pathology and treatment are presented.


2010 ◽  
Vol 90 (4) ◽  
pp. 415-416 ◽  
Author(s):  
Y Ishitsuka ◽  
K Ohara ◽  
F Otsuka

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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