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Relevant bibliographies by topics / Surgical resection of synovial sarcoma

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Academic literature on the topic 'Surgical resection of synovial sarcoma'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Surgical resection of synovial sarcoma"

1

Beck, Sarah E., G. Petur Nielsen, Kevin A. Raskin, and Joseph H. Schwab. "Intraosseous Synovial Sarcoma of the Proximal Tibia." International Journal of Surgical Oncology 2011 (2011): 1–5. http://dx.doi.org/10.1155/2011/184891.

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Synovial Sarcoma is a malignant mesenchymal tumor that comprises 5–10% of all soft tissue sarcomas. The mean age of onset is thirty years old. Intraosseous presentation is very rare and has only been documented a few times. We report herein a case of a 53-year-old man with synovial sarcoma arising in the left proximal tibia. The patient underwent a wide surgical resection and reconstruction, followed by adjuvant chemotherapy. Three years later, the patient developed a local recurrence that resulted in an above-the-knee amputation. Eight months later, the patient has completed chemotherapy and

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Gulum, Mehmet, Ercan Yeni, Murat Savas, et al. "Primary Renal Synovial Sarcoma." Case Reports in Urology 2011 (2011): 1–3. http://dx.doi.org/10.1155/2011/810184.

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Synovial sarcomas are generally deep-seated tumors that most often occur in the proximity of large joints of adolescents and young adults. We describe two cases of primary renal synovial sarcoma that were treated successfully by radical nephrectomy. Synovial sarcoma originating from the kidney is extremely rare and the histogenesis is uncertain. Surgical resection and ifosfamide based chemotherapy are the mainstay for the management of renal synovial sarcoma. Fewer than 40 patients have been described in the English literature. Physicians should be aware of the possibility of malignancy in cys

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Nakamura, Tomoki, Yuya Saito, Kunihiko Tsuchiya, et al. "Is perioperative chemotherapy recommended in childhood and adolescent patients with synovial sarcoma? A systematic review." Japanese Journal of Clinical Oncology 51, no. 6 (2021): 927–31. http://dx.doi.org/10.1093/jjco/hyab039.

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Abstract Objective Synovial sarcoma is the most common soft tissue sarcomas among childhood and adolescents, accounting for 8–10% of all soft tissue sarcoma. Synovial sarcoma is considered a relatively chemosensitive tumor compared with other soft tissue sarcomas. However, the role of perioperative chemotherapy in synovial sarcoma remains controversial. The purpose of this systematic review is to evaluate the role of perioperative chemotherapy in childhood and adolescent patients with synovial sarcoma. Methods We evaluated studies published between 1 January 1990 and 31 December 2017. The foll

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Corrales, C. E., G. Berry, and E. J. Damrose. "Primary cervical tracheal monophasic synovial sarcoma confirmed by SYT–SSX gene rearrangement." Journal of Laryngology & Otology 125, no. 6 (2011): 651–54. http://dx.doi.org/10.1017/s0022215110002975.

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AbstractObjective:To review the existing diagnostic modalities and treatment for primary tracheal synovial sarcoma, and to report a case of primary cervical synovial sarcoma arising in the trachea.Design:Retrospective.Setting:Head and neck surgery unit at a tertiary university centre.Patient:One case of primary cervical tracheal monophasic synovial sarcoma diagnosed by SYT–SSX gene rearrangement.Intervention:This patient underwent surgical resection of the synovial sarcoma, together with tracheal resection and primary anastomosis assisted by laryngeal-releasing manoeuvres, without complication

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Mistarihi, Dina, Anas Obaideen, Deborah Mukherji, and Walid Faraj. "Incidental intra-abdominal synovial sarcoma." BMJ Case Reports 16, no. 12 (2023): e255628. http://dx.doi.org/10.1136/bcr-2023-255628.

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Intra-abdominal synovial sarcomas are a rare type of soft tissue sarcomas that arise in the soft tissues of the abdominal cavity. They account for less than 1% of all primary synovial sarcoma cases. We report a case of a male patient in his early 30s who presented to the hospital with abdominal pain of 2 weeks duration. On examination, a mass was felt in the left mid-abdomen. MRI revealed a 12.7 cm×8.2 cm×8.6 cm soft tissue mass on the mesentery of the jejunum. The patient underwent surgical resection of the tumour, and the final pathology was synovial sarcoma, pT2b, grade 3.

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Bergene, Eyerusalem, and Dr Samuel Equar. "PAEDIATRIC-06 PEDIATRIC RECURRENT PRIMARY OCCIPITAL SYNOVIAL SARCOMA: A CASE REPORT." Neuro-Oncology Advances 5, Supplement_4 (2023): iv10. http://dx.doi.org/10.1093/noajnl/vdad121.040.

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Abstract BACKGROUND Synovial sarcoma is one of the malignant soft tissue sarcomas with an unknown histological origin. It has a unique t(X;18) (p11.2; q11.2) chromosomal translocation, resulting in the SYT-SSX fusion protein. The intracranial occurrence is mainly metastatic, and primary intracranial synovial sarcoma is extremely rare, with few case reports and case series in the literature.Surgical resection of the tumor followed by adjuvant radiotherapy and chemotherapy, regardless of the extent of tumor resection, has been shown to have a significant benefit. CASE PRESENTATION Here we report

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Krstic, Viktor, Milos Milosavljevic, Slobodanka Mitrovic, et al. "Synovial sarcoma of carotid space." Open Medicine 7, no. 4 (2012): 497–502. http://dx.doi.org/10.2478/s11536-012-0004-1.

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AbstractSynovial sarcomas are malignant tumors of mesenchymal origin, extremely rarely located in the area of the head and neck. Histologically they can be monophasic, biphasic or poorly differentiated with numerous differential diagnostic dilemmas. A 54-year-old male with synovial sarcoma of the carotid space is presented. The patient refused suggested postoperative radiotherapy and, nine months after the primary surgery, local relapse was verified. Following surgical resection of the local relapse, postoperative radiotherapy treatment was utilized. Ten months after the second surgery, second

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Lahlou, Chaimae, Hadj Hssain Ihssan, Meslouhi Kaoutar, et al. "Unprecedented presentation of pelvic synovial sarcoma: A compelling case report." Journal of Case Reports and Images in Oncology 10, no. 2 (2024): 20–25. http://dx.doi.org/10.5348/100137z10cl2024cr.

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Synovial sarcoma (SS) is a rare tumor that typically arises in various body regions, with its manifestation in the abdominal-pelvic area being exceptionally uncommon. However, despite its rarity in this location, it often metastasizes to the thorax. Despite its slow growth, it can be misdiagnosed as benign in less than 10% of cases. Diagnosis necessitates identification of the SYT-SSX fusion transcript, alongside immunohistochemical and cytogenetic assessments. Treatment involves surgical resection followed by radiotherapy for localized tumors, while chemotherapy is necessary for metastatic ca

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Georgeanu, V., T. Atasiei, D. Gartonea, B. Shazam, G. Goleşteanu, and Şt Cristea. "The Therapeutic Approach of Soft – Tissue Sarcomas. A 12 Cases Analysis." Romanian Journal of Orthopaedic Surgery and Traumatology 1, Supplement (2018): 58. http://dx.doi.org/10.2478/rojost-2018-0069.

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Abstract Introduction. Soft Tissue Sarcomas (STS) is a group of rare malignant tumors with mesenchymal tissue origin. At present, over 50 histopathological types with typical chromosome changes are described. Treatment is multidisciplinary, centered on the surgical approach. Method. Between 2014 and 2016, 12 STS cases were treated in our clinic: 3 liposarcomas, 2 synovial sarcomas, 1 angiosarcoma, 2 rhabdomyosarcomas, 2 myxofibrosarcomas, 1 fibroblast sarcoma and 1 clear cell sarcoma. With the exception of angiosarcoma that benefited only from chemotherapy, the other cases were surgically appr

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Dhiman, Sapna, Sarita Negi, Sandeep Moudgil, Jagdeep S. Thakur, and Ramesh K. Azad. "Synovial Sarcoma of Ethmoidal Sinus." Surgery Journal 07, no. 03 (2021): e195-e198. http://dx.doi.org/10.1055/s-0041-1731634.

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Abstract Background Synovial sarcoma is an aggressive soft tissue cancer of extremities mainly and rare in head and neck region, whereas rarest in ethmoidal sinus as only three cases have been reported till date. Case Reports We managed two cases of synovial sarcoma who presented with nasal obstruction, epistaxis, and swelling around the nasofacial region. Endoscopic nasal biopsy and immunohistochemistry markers confirmed synovial sarcoma in both the cases. While one case was managed by surgery and chemoradiation, the second patient received two cycles of ifosfamide-based chemotherapy and succ

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Book chapters on the topic "Surgical resection of synovial sarcoma"

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Anderson, Karen K., Paul M. Arnold, and Maura F. O’Neil. "Metastatic Spinal Cord Compression from Synovial Sarcoma: Surgical Resection." In Tumors of the Central Nervous System, Volume 10. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5681-6_32.

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Wu, Ming-Ho, I.-Ting Wang, Jen-Wei Tsai, and Chao-Tien Hsu. "Synovial Sarcoma in the Pleura." In Surgical Pathology. Springer Nature Singapore, 2025. https://doi.org/10.1007/978-981-97-8995-5_39.

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Özger, Harzem, and Buğra Alpan. "Alternative to Extra-Articular Resection in Synovial Sarcoma of the Knee." In Diagnosis and Treatment of Soft Tissue Tumors. Springer Nature Switzerland, 2025. https://doi.org/10.1007/978-3-031-77061-6_41.

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Takahashi, Hideaki E. "Case 4: Recurrent Synovial Sarcoma of the Pubic Region Treated with a Wide Resection, Including the Pubic Bone and Female Genitalia in a 50-Year-Old Woman." In Operative Treatment of Pelvic Tumors. Springer Japan, 2003. http://dx.doi.org/10.1007/978-4-431-66865-7_17.

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Gronchi, Alessandro, Angelo P. Dei Tos, and Paolo G. Casali. "Sarcomas of soft tissues and bone." In Oxford Textbook of Oncology. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199656103.003.0055.

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Sarcomas are rare tumours that can arise from bone or a variety of soft tissues in a variety of body sites. Surgery is the treatment mainstay for localized disease. Margins of resection are contingent on accurate histologic diagnosis. Adjuvant chemotherapy is routinely employed in osteosarcoma and Ewing Sarcomas, while it is used only on an individualized basis in high-risk soft tissue sarcoma. Isolated lung metastases from either bone or soft tissue sarcoma are primarily treated by surgery, especially if the disease-free interval is long and the number limited. Otherwise chemotherapy is the f

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Gronchi, Alessandro, Angelo P. Dei Tos, and Paolo G. Casali. "Sarcomas of soft tissues and bone and gastrointestinal stromal tumour." In Oxford Textbook of Oncology. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199656103.003.0055_update_001.

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Sarcomas are rare tumours that can arise from bone or a variety of soft tissues in a variety of body sites. Surgery is the treatment mainstay for localized disease. Margins of resection are contingent on accurate histologic diagnosis. Adjuvant chemotherapy is routinely employed in osteosarcoma and Ewing Sarcomas, while it is used only on an individualized basis in high-risk soft tissue sarcoma. Isolated lung metastases from either bone or soft tissue sarcoma are primarily treated by surgery, especially if the disease-free interval is long and the number limited. Otherwise chemotherapy is the f

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Lerut, Jan, and Quirino Lai. "Primary neoplasms of the liver." In Liver, Gall Bladder, and Bile Ducts, edited by Mohamed Rela, Pierre-Alain Clavien, Samiran Nundy, and Dirk J. Gouma. Oxford University PressOxford, 2023. http://dx.doi.org/10.1093/med/9780192862457.003.0019.

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Abstract Non-hepatocellular, non-cholangiocellular cancers are rare tumours which cover a broad spectrum. Their diagnostic and therapeutic algorithm is not standardized due to their rare occurrence, protean clinical manifestations, and evolution. This chapter gives an overview about the hepatic vascular tumours and about different types of sarcomatous tumours based on the analysis of the recent literature and the findings of the detailed European Liver Transplant Registry–European Liver Intestine Transplantation Association vascular tumour-study. Special attention is given to the role of liver

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Cairncross, Lydia, Francois Malherbe, and Dirk Strauss. "Tumours of the retroperitoneum and management of retroperitoneal sarcomas." In Abdominal Trauma, Peritoneum, and Retroperitoneum, edited by Aditya J. Nanavati, Sanjay Nagral, Samiran Nundy, and Dirk J. Gouma. Oxford University PressOxford, 2022. http://dx.doi.org/10.1093/med/9780192862433.003.0014.

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Abstract Retroperitoneal sarcomas (RPS) are rare tumours representing less than 0.3 per cent of all adult malignancies. Although rare, a knowledge of their presentation, workup and principles of management is important for primary care clinicians, radiologists and general surgeons, as early diagnosis and treatment is critical to the successful management of these complex and aggressive malignancies. Primary retroperitoneal tumours (RPT) arise separate from the organs of the retroperitoneum i.e. the kidneys, adrenals, pancreas and retroperitoneal colon. They may be benign or malignant and repre

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Conference papers on the topic "Surgical resection of synovial sarcoma"

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Pasetto, Camila Vitola, Diego Wallace Nascimento, Gabriela Bezerra Nóbrega, and José Roberto Filassi. "AXILLARY ACCESSORY BREAST SARCOMA IN A YOUNG PATIENT." In XXIV Congresso Brasileiro de Mastologia. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s1007.

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The accessory breast tissue in the axillary region is rare, but as there is breast tissue, there is the possibility of pathological degeneration. With an even greater rarity, breast sarcoma is a diverse group of malignancies derived from mesenchymal tissues. The aim of this report was to describe a case of a young patient with sarcomatous neoplasia in the axillary accessory breast topography. Patient LPMS, 19 years old, female, admitted to the mastology service of the Hospital das Clínicas of the Universidade de São Paulo with a nodule realized in the left axillary region with progressive grow

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Melo, Maria Eduarda Bernardino Martins, Darley de Lima Ferreira, Irnanda Layanna Gomes Oliveira, Julia Cavalcanti dos Santos Carneiro, and Gabriela Prado Lopes. "RECONSTRUCTION OF THE THORACIC WALL WITH EPIPLOON AND DERMO-CUT ABDOMINAL LOWER NEO FLAP IN BREAST ANGIOSARCOMA - CASE REPORT." In Scientifc papers of XXIII Brazilian Breast Congress - 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s1070.

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Introduction: Breast angiosarcoma is very rare and highly aggressive. It has an incidence of 0.5% to 1% of cases and its presentation is typically in women between 14 and 82 years of age with an average age that revolves around 35 years. Breast angiosarcoma presents clinically as a unilateral, softened tumor with ill-defined borders and skin thickening, with a variable growth rate. However, if compared to epithelial breast cancer, angiosarcoma has a faster growth rate. The second is known as stromal sarcoma, fibrosarcoma, leiomyosarcoma, histiocytoma, and giant cell sarcoma. Regarding adjuvant

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Ferreira, Darley, Nancy Ferreira, and Thais Ferreira. "RECONSTRUCTION OF THE THORACIC WALL WITH EPIPLOON AND ABDOMINAL LOWER DERMOCUTANEOUS RETAIL IN ANGIOSARCOMA MAMMARY." In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2102.

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Introduction: Breast angiosarcoma is a very rare and highly aggressive lesion, with an incidence of 0.5% to 1%. Berg et al. recognized two groups of sarcoma: the first group includes malignant phylloid cysts, lymphomas, and hemangiosarcomas, and the second group includes stromal sarcomas, fibrosarcomas, leiomyosarcomas, histiocytomas, and giant cell sarcoma. Angiosarcomas are lesions of indefinite and friable masses, with a mean age of 35 years. Case Report: A 35-year-old man from Paulo Afonso-PE presents complaining of breast lump. He underwent tumorectomy and confirmed fibroadenoma and phyll

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