نتایج جستجو برای: synovial sarcoma

تعداد نتایج: 88112  

Journal: :The Journal of bone and joint surgery. British volume 2005
A Matsumine K Kusuzaki H Hirata K Fukutome M Maeda A Uchida

We describe a case of intraneural metastasis of a synovial sarcoma, the first published case of a metastasis of a soft-tissue sarcoma to a peripheral nerve.

Journal: :The Medical journal of Malaysia 2011
L C Lina S Rosalind R Philip C Patricia Ann

Synovial sarcoma is a rare soft tissue sarcoma that commonly involves the lower extremities and occurs predominantly in young adults. It very rarely occurs in the head and neck region and carries a poor prognosis. The tumor demonstrates both a loco-regional and a systemic pattern of spread that makes management challenging. Combined modality therapy of this aggressive tumor yields better result...

Journal: :Annals of the Royal College of Surgeons of England 2008
Z Su J Zhang P Gao J Shi M Qi L Chen X Wang

This report outlines the work-up and management of a 35-year-old man with a synovial sarcoma of the lateral border of the tongue. Synovial sarcoma of the tongue is an extremely rare tumour with variable morphological microscopic types and characters of immunohistochemical profile. There have only been 15 cases previously reported. This report aims to update the literature on this subject and ex...

2017
Kelechukwu U Okoro Matthew D Roby David C Sane Robert E Budin

Primary cardiac sarcoma is a rare malignant myocardial neoplasm that does not exhibit gender predominance or age predilection. The classification of these tumors includes several subtypes, of which synovial sarcoma is a rare manifestation. When present, these tumors portend a poor prognosis with high morbidity and mortality that is attributable to their inherent infiltrative capacity, especiall...

2014
H. Krishna Moorthy Biju S. Pillai Jophy Varghese

Primary renal synovial sarcoma is a rare tumor having a specific chromosomal translocation t(X; 18) (p11.2; q11.2). The clinical features of this tumor and radiologic appearances are quite similar to those of renal cell carcinoma. Confirmatory diagnosis requires fluorescent in situ hybridization or reverse transcriptase polymerase chain reaction validation for differentiating the tumors from sa...

Journal: :Romanian Journal of Rhinology 2021

Abstract BACKGROUND. Synovial sarcomas of the soft tissue are a particular type that rarely appear in head and neck region. CASE REPORT AND COMMENTS. We present case 27-year-old patient diagnosed 2017 with palate biphasic synovial sarcoma who presented recurrent microepistaxis, nasal obstruction, left cephalalgia aural fullness ear. The clinical examination showed tumor approximately 4/6 cm dia...

2016
Elizabeth L McKinnon Thomas J Cummings Xiaoyin Sara Jiang

Synovial sarcoma is a soft tissue malignancy that generally arises adjacent to joint capsules. The development of this entity in the abdomen is an uncommon presentation. We present a case of a 38-year old male who presented to the emergency room with anemia and abdominal pain. The patient was found to have hemoperitoneum, and on imaging the patient was also noted to have nodular lesions of the ...

Journal: :Journal of Ayub Medical College, Abbottabad : JAMC 2015
Nabila Javed Javed Iqbal

Synovial sarcoma is a mesenchymal spindle cell tumour that displays variable epithelial differentiation. It most commonly occurs in lower extremities. Head and neck is a rare site for synovial sarcoma accounting for less than 10%. Larynx is an extremely rare site and only 16 cases with laryngeal location have been reported. Immunohistochemistry is important for correct diagnosis. Surgical excis...

2009
Benjamin Henninger Martin Freund Bettina Zelger Daniel Putzer Hugo Bonatti Ludwig Müller Michael Fiegl Christian Geltner

Primary mediastinal synovial sarcoma is a rare malignancy with only a few cases reported so far. A 56-year-old woman was admitted to our hospital for an investigation of a nodule in the left middle lung on chest radiography. Computed tomography revealed a mediastinal mass first described as a solitary fibrous tumor. The diagnosis of synovial sarcoma was established by computed tomography-guided...

2017
Takahito Kondo Yukiko Sato Hiroko Tanaka Toru Sasaki Kazuyoshi Kawabata Hiroki Mitani Hiroyuki Yonekawa Hirofumi Fukushima Wataru Shimbashi

Ectopic hamartomatous thymoma (EHT) is an extremely rare benign tumor. EHTs are difficult to differentiate from sarcomas, especially synovial sarcomas. We encountered two cases of EHT that were referred from other hospitals because sarcoma was suspected. In these cases, fusion gene detection via polymerase chain reaction or fluorescence in situ hybridization was useful for differentiating EHT f...

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