Synovial Sarcoma Kidney //

Sep 10, 2015 · Synovial sarcoma is a rare and aggressive soft tissue sarcoma. In the early stages of the condition, it may cause no noticeable signs or symptoms. However, as the tumor grows larger, affected people may notice a lump or swelling. In some cases, the tumor can limit range of motion or cause numbness and/or pain if it presses on nearby nerves. May 26, 2018 · Synovial sarcoma Synovial sarcoma is a rare type of cancer that tends to arise near large joints, particularly the knee, in young adults. Despite its name, it typically doesn't affect the interior of joints, where synovial tissue and fluid are located. The first sign of trouble is usually a deep-seated lump that may be tender or painful. Aug 02, 2017 · Synovial sarcoma is a rare type of soft tissue sarcoma, or cancerous tumor. About one to three people in a million receive a diagnosis of this disease each year. Anyone can. Three histologic subtypes of synovial sarcoma are noted: monophasic, biphasic, and poorly differentiated. There is a clinical challenge to diagnose it. As spindle cell morphology its differential diagnosis would be sarcomatoid renal cell sarcoma, primary Ewing sarcoma of kidney, adult Wilms tumour, and undifferentiated carcinoma. The renal parenchyma is a rare site of origin for primary synovial sarcoma SS. The present study describes the clinicopathologic, immunohistochemical, and molecular analysis of 7 cases of SS occurring in the kidney. There were 5 female and 2 male patients, with an age range of 15 to 46 years.

Synovial sarcoma is a kind of soft tissue sarcoma, which is a type of cancer that arises from soft tissues near the joints but can sometimes develop in the kidney and lung. Despite its name and its location near the joints, synovial sarcoma does not arise from actual. Primary synovial sarcoma arising from the kidney is extremely rare. We report two cases with primary renal synovial sarcoma. Both were initially diagnosed as renal cell carcinoma. The first case was a 30-year-old woman who presented with right flank soreness. Synovial sarcoma is a cancer that can come from different types of soft tissue, such as muscle or ligaments. It is often found in the arm, leg, or foot, and near joints such as the wrist or ankle. It can also form in soft tissues in the lung or abdomen. Synovial sarcoma may also be called malignant synovioma. The biology of synovial sarcoma probably falls between most typical adult soft tissue sarcomas and paediatric small round cell tumors such as rhabdomyosarcoma or Ewing’s sarcoma. The response rate to chemotherapy, in fact, is approximately 60% for synovial sarcoma, less than 40% for adult soft tissue sarcomas and 80% for rhabdomyosarcoma.

A synovial sarcoma also known as: malignant synovioma is a rare form of cancer which occurs primarily in the extremities of the arms or legs, often in proximity to joint capsules and tendon sheaths. It is a type of soft tissue sarcoma. Mucinous, gland predominant synovial sarcoma of a large peripheral nerve: a rare case closely mimicking metastatic mucinous carcinoma. J Clin Pathol. 2008 May;615:672-6. Kosemehmetoglu K, Vrana JA, Folpe AL. TLE1 expression is not specific for synovial sarcoma: a whole section study of 163 soft tissue and bone neoplasms.

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