scholarly journals A Rare Case of Synovial Sarcoma Involving the Brachial Plexus

2011 ◽  
Vol 2 (1) ◽  
pp. 24-26 ◽  
Author(s):  
Anand Vasant Ghiya ◽  
Mrunal Nitin Ketkar ◽  
Shilpa Patankar ◽  
Sudhir Kothari
Keyword(s):  
Brachial Plexus ◽  
Synovial Sarcoma ◽  
Rare Case

scholarly journals A Rare Case of Synovial Sarcoma Involving the Brachial Plexus, Treated with Wide Local Excision and Reconstructed with Sural Nerve Grafts

2019 ◽  
Vol 10 (3) ◽  
pp. 435-436
Author(s):  
Kuldeepsinh Pradipkumar Atodaria ◽  
Nikunj KishorkumarVithalani ◽  
Atul Gajendra Bharambe ◽  
Bharat Chandra Mishra ◽  
Keshvi Mahendrasinh Chauhan
Keyword(s):  
Brachial Plexus ◽  
Synovial Sarcoma ◽  
Local Excision ◽  
Wide Local Excision ◽  
Sural Nerve ◽  
Rare Case ◽  
Nerve Grafts

PLEXIFORM NEUROFIBROMA OF THE BRACHIAL PLEXUS – A RARE CASE REPORT

2021 ◽  
pp. 13-15
Author(s):  
Surya Rao Rao Venkata Mahipathy ◽  
Alagar Raja Durairaj ◽  
Narayanamurthy Sundaramurthy ◽  
Anand Prasath Jayachandiran ◽  
Suresh Rajendran
Keyword(s):  
Brachial Plexus ◽  
Rare Case ◽  
Autosomal Dominant ◽  
Plexiform Neurofibroma ◽  
Autosomal Dominant Disorder ◽  
Surgical Debulking ◽  
Rare Case Report ◽  
Benign Tumours ◽  
Common Benign Tumour

Neurobroma is a common benign tumour occurring as part of an autosomal dominant disorder, neurobromatosis type 1, leading to the formation of benign tumours or neurobromas of the peripheral nervous system. Large neurobromas of the brachial plexus are rare and present a difcult challenge for surgeon due to the anatomical complexity of the brachial plexus. Dermal neurobromas usually present with swelling and occasional pain, but neurobromas associated with the brachial plexus present with pain and neurological symptoms. These plexiform neurobromas of the brachial plexus are known to undergo malignant transformation. Here, we present a case of a large plexiform neurobroma affecting the left brachial plexus and extending till the elbow, conrmed with MRI and surgical debulking was done.

scholarly journals Synovial sarcoma of the brachial plexus – a rare tumor in a rare area: a case report

2018 ◽  
Vol 12 (1) ◽  
Author(s):  
Sreekanth Raveendran ◽  
Albert Abhinay Kota ◽  
Edwin Stephen ◽  
Samuel C. R. Pallapati ◽  
Binu Prathap Thomas
Keyword(s):  
Case Report ◽  
Brachial Plexus ◽  
Synovial Sarcoma ◽  
Rare Tumor

scholarly journals Unresectable retrovesical synovial sarcoma treated by chemotherapy and radiotherapy: A rare case report

2019 ◽  
Vol 4 (2) ◽  
Author(s):  
Mohammed Afif ◽  
Saoussan Kharmoum ◽  
Youssef Omor ◽  
Jihane Khalil ◽  
Mohamed Elhfid
Keyword(s):  
Case Report ◽  
Synovial Sarcoma ◽  
Rare Case ◽  
Rare Case Report

A rare case of metastatic cardiac synovial sarcoma

2018 ◽  
Vol 2 (1) ◽  
pp. 82
Author(s):  
SurajKumar Kulkarni ◽  
CN Manjunath ◽  
S Shankar ◽  
SS Prakash ◽  
Shivakumar Bhairappa ◽  
...  
Keyword(s):  
Synovial Sarcoma ◽  
Rare Case ◽  
Cardiac Synovial Sarcoma

scholarly journals 256 Monophasic Synovial Sarcoma Presenting as a Parapharyngeal Mass—Report of a Rare Case

2018 ◽  
Vol 149 (suppl_1) ◽  
pp. S109-S109
Author(s):  
Faisal Saeed ◽  
Taliya Farooq ◽  
Yasmin Yusuf
Keyword(s):  
Synovial Sarcoma ◽  
Rare Case

Synovial Sarcoma of the Brachial Plexus

Neurosurgery ◽  
2011 ◽  
Vol 70 (5) ◽  
pp. 1329-1333 ◽  
Author(s):  
Farhad Pirouzmand ◽  
Kavya Kommaraju ◽  
Kenneth J. Craddock ◽  
David Howarth
Keyword(s):  
Brachial Plexus ◽  
Synovial Sarcoma ◽  
Soft Tissue Tumor ◽  
Clinical Presentation ◽  
Clinical Course ◽  
Relevant Literature ◽  
Adjuvant Radiation ◽  
Malignant Soft Tissue Tumor ◽  
Malignant Soft Tissue ◽  
Firm Mass

Abstract BACKGROUND AND IMPORTANCE: Synovial sarcoma (SS) is a malignant soft-tissue tumor that rarely involves brachial plexus. The authors report a case of brachial plexus SS and review the relevant literature. CLINICAL PRESENTATION: A 53-year-old woman presented with gradually enlarging right subclavicular mass over 5 years associated with sharp aching pain radiating down toward the radial 3 fingers. On examination, she had a corresponding firm mass in the supraclavicular region with a positive Tinel sign. There was no objective neurological deficit. She underwent partial excision of this mass without any further adjuvant radiation or chemotherapy. Pathology was consistent with SS. CONCLUSION: Lack of any recurrence in this case 6 years after incomplete excision with no adjuvant therapy suggests slow clinical course in some of these sarcomas.

scholarly journals Rare case of synovial sarcoma of anterior abdominal wall in a young Indian male

2017 ◽  
Vol 4 (7) ◽  
pp. 2358
Author(s):  
Abhishek Katyal ◽  
Yash Patel
Keyword(s):  
Abdominal Wall ◽  
Synovial Sarcoma ◽  
Rare Case ◽  
Anterior Abdominal Wall ◽  
Close Association ◽  
Abdominal Cavity ◽  
Typically Develop ◽  
Synovial Sarcomas ◽  
Upper Abdominal ◽  
Malignant Soft Tissue

Synovial Sarcomas (synoviomas) are the fourth most common malignant soft-tissue tumours, and typically develop in para-articular locations of the extremities in close association with joint capsules, tendon sheaths, bursae and fascial structures. Other less common sites include the head and neck, abdominal wall, intra-abdominal cavity, and mediastinum. In this article, an interesting and rare case of a 25-year-old man with left upper abdominal lump is reported which was subsequently diagnosed as biphasic synovial sarcoma (spindle cell variety) of anterior abdominal wall. 

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