scholarly journals GIST of Mesocolon: A Case Report

2012 ◽  
Vol 10 (1) ◽  
pp. 37-39
Author(s):  
S Malla ◽  
SB Rawal ◽  
NK Giri
Keyword(s):  
Medical Journal ◽  
Case Report ◽  
Clinical Practice ◽  
Soft Tissue ◽  
Gastrointestinal Stromal Tumor ◽  
World Literature ◽  
Rare Case ◽  
Soft Tissue Tumor ◽  
Tissue Tumor ◽  
The World

Gastrointestinal Stromal Tumor (GIST) is a rare soft tissue tumor and a GIST arising from the mesocolon is even rarer and sparsely reported in the world literature. Herein we report one such case that we encountered in our clinical practice and review the literature on the management of such a rare case. DOI: http://dx.doi.org/10.3126/mjsbh.v10i1.6448 Medical Journal of Shree Birendra Hospital Jan-June 2011 10(1) 37-39

scholarly journals A case of soft-tissue tumor over the sternum: A rare case report

2021 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
SagarDilip Rathod ◽  
Dhirendra Wagh ◽  
S Niveditha
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Soft Tissue Tumor ◽  
Tissue Tumor ◽  
Rare Case Report

scholarly journals Mass on thigh mimicking soft tissue tumor – a rare case report

2015 ◽  
Vol 1 (1) ◽  
pp. 25-29
Author(s):  
Dr. Ezhil Arasi. N ◽  
◽  
Anunayi. J ◽  
Lakshmi Surekha. M ◽  
Naga Kalyani. P ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Soft Tissue Tumor ◽  
Tissue Tumor ◽  
Rare Case Report

scholarly journals Management of a soft tissue tumor in a child with Worster Drought syndrome using 810 nm diode laser - A case report

LASER THERAPY ◽  
2015 ◽  
Vol 24 (2) ◽  
pp. 113-117
Author(s):  
Praveen Kumar Jayakumar ◽  
Jayakumar Paramasivam ◽  
Naveen Kumar Jayakumar ◽  
Gayathri Praveen Kumar ◽  
Alex Mathews Muruppel
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Diode Laser ◽  
Soft Tissue Tumor ◽  
Tissue Tumor

Congenital cholesteatoma in identical twins

2012 ◽  
Vol 127 (1) ◽  
pp. 67-69 ◽  
Author(s):  
T Al Balushi ◽  
J Z Naik ◽  
M Al Khabori
Keyword(s):  
Case Report ◽  
World Literature ◽  
Rare Case ◽  
Identical Twins ◽  
Rare Entity ◽  
Ear Surgery ◽  
Congenital Cholesteatoma ◽  
The World ◽  
Local Trauma ◽  
Clinical Pictures

AbstractObjective:We present an extremely rare case of congenital cholesteatoma in identical twins.Method:Case report of congenital cholesteatoma in identical twins, and a literature review, are presented.Results:Both cases presented to the ENT out-patient clinic, but with different clinical pictures. Both were managed surgically.Conclusion:Congenital cholesteatoma presents as a whitish mass in the middle ear, with an intact tympanic membrane. It is a rare entity comprising between 3.7 and 24 per cent of total cholesteatoma cases. The key to its diagnosis is the absence of previous ear infection, ear surgery and local trauma. To our best knowledge, this paper represents the first report in the world literature of congenital cholesteatoma in identical twins.

Congenital cholesteatoma of occipital bone or intradiploic epidermoid cyst? One and the same disease

2008 ◽  
Vol 123 (6) ◽  
pp. 673-675 ◽  
Author(s):  
M P A Clark ◽  
P M Pretorius ◽  
D Beaumont ◽  
C A Milford
Keyword(s):  
Case Report ◽  
Middle Ear ◽  
Epidermoid Cyst ◽  
World Literature ◽  
Rare Case ◽  
Occipital Bone ◽  
Epidermoid Cysts ◽  
Congenital Cholesteatoma ◽  
Imaging Characteristics ◽  
The World

AbstractObjective:We report an extremely rare case of congenital cholesteatoma affecting the occipital bone.Methods:We present a case report, plus a review of the world literature on similar lesions.Results:This case report describes the presentation and treatment of a congenital cholesteatoma arising in an apparently unique location within the occipital bone, with no effect on middle-ear structure or function. The different imaging characteristics of this lesion are described and illustrated. The discussion centres on the differentiation of this lesion from intradiploic epidermoid cysts, more commonly described in the neurosurgical literature. The possible methods of pathogenesis are discussed, along with treatment suggestions.Conclusion:Congenital cholesteatomas and intradiploic epidermoid cysts are indistinguishable both histologically and radiologically, and would appear to be the same disease.

scholarly journals IgG4-Related Disease Presenting as a Soft Tissue Tumor Affecting Skeletal Muscle: A Case Report

2013 ◽  
Vol 04 (12) ◽  
pp. 1-4 ◽  
Author(s):  
David Sáez Martínez ◽  
Felipe López Oliva ◽  
María Jesús Fernández Aceñero ◽  
Elena Fontoira Moyer ◽  
Juan Luis Arranz Cozar
Keyword(s):  
Skeletal Muscle ◽  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Related Disease ◽  
Tissue Tumor ◽  
Igg4 Related Disease

scholarly journals Lipomas of Larynx: The Rare Entities

2012 ◽  
Vol 2 (2) ◽  
pp. 79-81 ◽  
Author(s):  
Somanath B Megalamani ◽  
Ravindra Gadag ◽  
A Raza ◽  
A Satish
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Spindle Cell ◽  
Anterior Commissure ◽  
The Body ◽  
Spindle Cell Lipoma ◽  
Tissue Tumor

ABSTRACT Lipoma is the commonest soft tissue tumor arising anywhere in the body, but its occurrence in the larynx is relatively rare. We present a rarest case of lipoma with cartilaginous metaplasia arising from the larynx just above the anterior commissure. The second case report is about a large spindle cell lipoma of larynx presented with stridor. How to cite this article Megalamani SB, Gadag R, Raza A, Satish A. Lipomas of Larynx: The Rare Entities. Int J Phonosurg Laryngol 2012;2(2):79-81.

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