A Large Malignant Glomus Tumor involving Bones and Soft tissues of the Wrist: A Rare Case Report

2016 ◽  
Vol 5 (2) ◽  
pp. 195-198
Author(s):  
Bharat Rekhi ◽  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Soft Tissues ◽  
Glomus Tumor ◽  
Rare Case Report

scholarly journals Complete Ossification of the Stylohyoid Chain as Cause of Eagle's Syndrome: A Very Rare Case Report

2014 ◽  
Vol 15 (4) ◽  
pp. 500-505 ◽  
Author(s):  
Antônio Sérgio Guimarães ◽  
Daniel Humberto Pozza ◽  
Idercy Cabral de Castro ◽  
Iván Claudio Suazo Galdames ◽  
Sandro Palla
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Soft Tissues ◽  
Surgical Excision ◽  
Styloid Process ◽  
Eagle’S Syndrome ◽  
Elongated Styloid Process ◽  
Rare Case Report ◽  
The Right ◽  
Stylohyoid Chain

ABSTRACT Aim To report on a patient with Eagle's syndrome with a complete and very large ossification of the stylohyoid complex on the right side that to our best knowledge has never been published previously. Background Eagle's syndrome is characterized by a set of symptoms that are caused by the irritation of the neurovascular and soft-tissues caused by an elongated styloid process or ossification of stylohyoid ligament. Case description Because of the high discomfort and pain degree as well as limitations of mandibular and head mobility and also the thickness of the ossified stylohyoid chain, the patient was treated surgically by removing the hypertrophic segment. Conclusion These symptoms subsided completely after the surgical excision of the anomaly. The elongated styloid process on the left side was symptom free. Clinical significance Eagle's syndrome symptoms are not specific and can mimic those of other disorders, the syndrome must be included in the differential diagnosis of patients with pain in the orofacial, pharyngeal and cervical area. How to cite this article Guimarães AS, Pozza DH, de Castro IC, Galdames ICS, Palla S. Complete Ossification of the Stylohyoid Chain as Cause of Eagle's Syndrome: A Very Rare Case Report. J Contemp Dent Pract 2014;15(4):500-505.

Glomus Tumor of the Pterygopalatine Fossa: A Rare Case Report

2020 ◽  
Author(s):  
Pankaj Chauhan ◽  
Trilok C. Guleria ◽  
R. S. Minhas ◽  
Suresh Thakur ◽  
Mahender Singh ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Glomus Tumor ◽  
Pterygopalatine Fossa ◽  
Rare Case Report

scholarly journals HEMANGIOPERICYTOMA OF PALATE A RARE CASE REPORT

2021 ◽  
Vol 9 (07) ◽  
pp. 863-866
Author(s):  
Sushmita Batra ◽  
Pramod Krishna B. ◽  
Rajdeep Singh ◽  
Amy E. Thomas ◽  
Surabhi Singhai
Keyword(s):  
Blood Flow ◽  
Case Report ◽  
Oral Cavity ◽  
Rare Case ◽  
Soft Tissues ◽  
External Surface ◽  
Review Of Literature ◽  
Vascular Tumour ◽  
High Propensity ◽  
Rare Case Report

The Hemangiopericytoma is a rare vascular tumour originating from the pericytes, which are found on the external surface of the capillaries and are thought to act as a sphincter that controls blood flow. It has a high propensity for recurrence and metastasis.The tumor usually develops as a slowly enlarging painless mass.It typically occurs in the soft tissues of the extremities and trunk, and is rarely seen in the oral cavity.15–16% are seen in the head and neck region.The most common sites of involvement are scalp, face, neck, nasal cavities and paranasal sinuses. Involvement of the palate is extremely rare and so here weare presenting a case of hemangiopericytoma of palate, its diagnosis, management and a brief review of literature.

scholarly journals Primary glomus tumor of the liver: A rare case report and review of the literature

2011 ◽  
Vol 54 (3) ◽  
pp. 584 ◽  
Author(s):  
Bita Geramizadeh ◽  
Saman Nikeghbalian ◽  
Alireza Shamsaifar ◽  
Kourosh Kazemi ◽  
Hassan Tavoosi ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Glomus Tumor ◽  
Review Of The Literature ◽  
Rare Case Report

scholarly journals Osteochondroma of the Parapharyngeal Space: A Rare Case Report

2013 ◽  
Vol 5 (4) ◽  
pp. 30-32
Author(s):  
Ashok K Gupta ◽  
Karan Gupta ◽  
Kim Vaiphei ◽  
Darwin Kaushal
Keyword(s):  
Case Report ◽  
Malignant Transformation ◽  
Rare Case ◽  
Soft Tissues ◽  
Parapharyngeal Space ◽  
Histopathological Examination ◽  
Rare Case Report

ABSTRACT Extraskeletal osteochondroma in parapharyngeal space is very rare. It is important to note that such a diagnosis be considered when a discrete, ossified mass is localized in soft tissues, even at atypical sites. Its diagnosis is based on radiological and histopathological examination. We should be clinically aware of this benign entity as no malignant transformation or metastasis has been reported. Excision with adequate cuff of tissue is treatment of choice. We did not encounter any case report of osteochondroma in the parapharyngeal space in literature, with our best possible effort.

scholarly journals Glomus tumor of the anterior urethra: A rare case report and review of the literature

2016 ◽  
Vol 4 (6) ◽  
pp. 1057-1059 ◽  
Author(s):  
TAO HE ◽  
JIA HU ◽  
LU JIN ◽  
YIFAN LI ◽  
JIAJU LIU ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Glomus Tumor ◽  
Review Of The Literature ◽  
Anterior Urethra ◽  
Rare Case Report

Intraosseous glomus tumor of distal phalanx thumb -A rare case report

2017 ◽  
Vol 4 (2) ◽  
pp. 137-140
Author(s):  
Ruchi Rathore ◽  
◽  
Deepshikha Arora ◽  
Ankit Jain ◽  
Sarla Agarwal ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Glomus Tumor ◽  
Distal Phalanx ◽  
Rare Case Report

scholarly journals Disseminated Extramedullary Plasmacytoma with Unusual Cardiac and Pancreatic Involvement—Literature Review and Rare Case Report

2021 ◽  
Author(s):  
S. Babu Peter ◽  
V. Raghu Nandhan ◽  
R. Sandhiya
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Soft Tissues ◽  
Extramedullary Plasmacytoma ◽  
Imaging Features ◽  
Clinical Scenario ◽  
Pancreatic Involvement ◽  
Rare Case Report ◽  
Work Up ◽  
Detailed Work

AbstractDisseminated extramedullary plasmacytoma (EMP) is an unusual entity that has nonspecific imaging features at MRI. Nevertheless, knowledge of its imaging features and unusual locations might help radiologists to suspect it in the appropriate clinical scenario. Some noncontiguous EMPs might mimic lymphoma and MRI would be useful as a problem-solving tool in EMP and would help in treatment planning. We report an unusual cardiac mass in cardiac MRI, a detailed work-up of which led to the diagnosis of multifocal EMP involving the heart, ribs, pancreas, retroperitoneum, and soft tissues of the thigh, rarely reported in the literature.

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