Adult Renal Sarcoma: Clinical Features and Survival in a Series of Patients Treated at a High-volume Institution

Wang, Xianding; Xu, Ruiling; Yan, Libo; Zhuang, Jing; Wei, Bing; Kang, Deying; Wu, Ke; Xie, Linlin; Xie, Zhiyuan; Wang, Qiang; Li, Xiang; Zeng, Hao; Lu, Yiping

doi:10.1016/j.urology.2010.09.028

Cited by 30 publications

(30 citation statements)

References 22 publications

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“…Both lesions are rare. Adult renal sarcoma accounts for 0.8% of renal cancer cases and generally has a poor prognosis [21]. RCC with sarcomatoid features is also associated with a poor prognosis, but unlike renal carcinoma targeted therapy has no clear benefits [22].…”

Section: Discussionmentioning

confidence: 99%

“…RCC with sarcomatoid features is also associated with a poor prognosis, but unlike renal carcinoma targeted therapy has no clear benefits [22]. Treatment of inferior vena cava tumour thrombus should be based on the primary pathology and natural behaviour of a given tumour in a specific patient rather than only focusing on the level and extent of venous invasion [21]. …”

Section: Discussionmentioning

confidence: 99%

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Sarcomatoid Variant of Urothelial Carcinoma of the Renal Pelvis with Inferior Vena Cava Tumour Thrombus: A Case Report and Literature Review

Rashid

Akhtar

2018

Case Reports in Pathology

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Sarcomatoid variant of urothelial carcinoma (SVUC) of the renal pelvis is a rare entity. To the best of our knowledge, around 25 cases of this neoplasm have been reported in the literature to date, most of which were of high stage. The inferior vena cava tumour thrombus, which is a hallmark of renal cell carcinoma (RCC), may rarely be found in urothelial carcinoma of renal pelvis. In this report, a case of SVUC associated with tumour extension to inferior vena cava is documented. This association has been encountered in only one previously reported case. The possibility of urothelial carcinoma of the renal pelvis should therefore be included in the differential diagnosis of tumour thrombus of the inferior vena cava.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Sarcomatoid Variant of Urothelial Carcinoma of the Renal Pelvis with Inferior Vena Cava Tumour Thrombus: A Case Report and Literature Review

Rashid

Akhtar

2018

Case Reports in Pathology

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“…Wang et al analyzed 41 cases of renal sarcoma from 1989 to 2009. The most common histological subtype was leiomyosarcoma in 16 patients (39%), followed by liposarcoma in 12 (29.3%), and other in 13 (31.7%) . Diagnosis of renal sarcoma can be made through radiological and histological techniques by using biomarkers such as desmin, vimentin, neuron‐specific enolase, and S‐100.…”

Section: Discussionmentioning

confidence: 99%

Adult renal sarcoma: A rare case of recurrence 13 years after initial resection

Alameddine

Zheng

Yusufali

et al. 2018

Clinical Case Reports

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Key Clinical MessageRenal sarcoma is a rare and aggressive malignancy without proper guidelines for treatment. Due to the aggressiveness of this disease and the potential for recurrence, we believe that extensive surgical resection with healthy margins may be the best option to treat this condition during both initial resection and resection of the recurrent lesion. Clinical follow‐up is also important to monitor for tumor recurrence.

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“…The most common sign at presentation was abdominal mass and the predominant histologic subtype was leiomyosarcoma. In Wang et al study, approximately 15% of the patients had metastatic disease at diagnosis 47 . Most of the patients died in the first 3 years following surgery.…”

Section: Genetic and Molecular Factorsmentioning

confidence: 93%

Renal sarcoma – a rare parenchymal tumor with a very poor prognosis

Iorga¹,

Anghel²,

Marcu³

et al. 2018

Arch Balk Med Union

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Le sarcome rénal-une tumeur parenchymateuse rare avec un pronostic très mauvais Le but de cet article était d'analyser les caractéristiques pronostiques, la présentation clinique, le diagnostic et le traitement des sarcomes rénaux primaires. Une revue approfondie de la littérature a été réalisée à l'aide de la base de données PubMed. Les sarcomes du rein sont des tumeurs malignes très rares, avec un très mauvais pronostic par rapport aux autres sarcomes urogénitaux. Plusieurs types histologiques ont été rapportés, le type le plus courant étant le léiomyosarcome. Outre la résection chirurgicale complète à larges marges, des facteurs anatomiques, histologiques, moléculaires

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Adult Renal Sarcoma: Clinical Features and Survival in a Series of Patients Treated at a High-volume Institution

Cited by 30 publications

References 22 publications

Sarcomatoid Variant of Urothelial Carcinoma of the Renal Pelvis with Inferior Vena Cava Tumour Thrombus: A Case Report and Literature Review

Sarcomatoid Variant of Urothelial Carcinoma of the Renal Pelvis with Inferior Vena Cava Tumour Thrombus: A Case Report and Literature Review

Adult renal sarcoma: A rare case of recurrence 13 years after initial resection

Renal sarcoma – a rare parenchymal tumor with a very poor prognosis

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