Synovial Sarcoma of the Nerve—Clinical and Pathological Features: Case Series and Systematic Review

Burks, S. Shelby; Puffer, Ross C.; Cajigas, Iahn; Valdivia, David; Rosenberg, Andrew E.; Spinner, Robert J.; Levi, Allan D.

doi:10.1093/neuros/nyz321

Cited by 6 publications

(3 citation statements)

References 57 publications

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“…Therefore, a high rate of local recurrence and metastasis was observed, while data showed that the survival rate was 20% to 50% in the last 5 years. [ 7 ]…”

Section: Discussionmentioning

confidence: 99%

Primary renal synovial sarcoma

Zhang

Tian

et al. 2020

Medicine

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Rationale: Synovial sarcoma (SS) is a malignant neoplasm that arises from soft tissues proximal to the joints. It occurs primarily at the major joints of the extremities, but may also occur in the deep soft tissues around the joints. While primary renal synovial sarcoma (PRSS) is extremely rare, it is important to have a better understanding of their imaging and clinical features to establish an effective treatment plan. Correct identification of PRSS is also useful for treating renal neoplasms. Patient's concerns: A 56-year-old Chinese man was admitted to our hospital due to moderate, paroxysmal left-sided loin pain. Diagnosis: Renal enhanced computed tomography (CT) scanning showed a relatively hypovascular lesion with calcification in the left kidney. A radical nephrectomy was performed in the left kidney. Postoperative pathology indicated SS with necrosis. The immunohistochemical findings were as follows: 34βE12 (Epithelium+), Bcl-2(+), CD99(+), CK-pan((Epithelium+), EMA(Epithelium+), Ki-67(+60%), and Vimentin(+), CD34(−). Interventions: The patient underwent radical left nephrectomy with no complications. Outcomes: After discharge, a close review for 3 months showed no evidence of recurrence. Lessons: PRSS should be considered for the differential diagnosis of renal hypovascular tumors. When problems arise in distinguishing renal hypovascular tumors, surgical pathology is helpful in the final diagnosis and further treatment of the disease.

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“…Therefore, a high rate of local recurrence and metastasis was observed, while data showed that the survival rate was 20% to 50% in the last 5 years. [ 7 ]…”

Section: Discussionmentioning

confidence: 99%

Primary renal synovial sarcoma

Zhang

Tian

et al. 2020

Medicine

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“… 1 2 According to the reported series, the main symptoms are neuropathic and local pain, motor deficit, and palpable mass; in our patient, the insidious symptomatology and history of rheumatic disease delayed the diagnosis. 3 …”

Section: Discussionmentioning

confidence: 99%

“… 1 2 De acordo com a série relatada, os principais sintomas são dor neuropática e local, déficit motor e massa palpável; em nosso paciente, a sintomatologia insidiosa e a história da doença reumática atrasaram o diagnóstico. 3 …”

Section: Discussionunclassified

Sarcoma sinovial insidioso de osso em um paciente com artrite reumatoide

Reyes-Villarreal

Pineda-Galindo

Vera‐Lastra

et al. 2021

Rev Bras Ortop (Sao Paulo)

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ResumoSarcoma sinovial é uma rara malignidade de origem mesenquimal; a abordagem diagnóstica geralmente começa documentando um tumor de tecido mole; no entanto, resulta em um diagnóstico desafiador quando é mais profundo, de pequeno porte ou primário do osso.O presente relato descreve um paciente que apresentou dor insidiosa no quadril atribuída a artrite reumatoide, com desfecho fatal devido a doenças de base e complicações cirúrgicas.A subestimação da dor no quadril, principalmente quando não há massa palpável, pode atrasar o diagnóstico.

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