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leiomyosarcoma/fièvre

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OBJECTIVE Whole-body hyperthermia (WBH) in combination with chemotherapy is a relatively new promising treatment modality for patients with cancer. The objective of this report is to present the development of an acute systemic inflammatory response syndrome (SIRS) with multiple organ dysfunction

Leiomyosarcoma of the Broad Ligament With Fever Presentation: A Case Report and Review of Literature.

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BACKGROUND Leiomyosarcoma is a rare gynecologic malignancy that accounts for less than 1% of gynecological malignancies. Leiomyosarcoma of the broad ligament is an even rarer condition. According to Gardner's criteria, the diagnosis is made when the mass is completely separated from the uterus and

Complete disappearance of a leiomyosarcoma of the lower extremity following preoperative hyperthermia and intra-arterial doxorubicin.

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Leiomyosarcoma of the extremities is an unusual tumor. Herein we report a unique and what we believe is the first case of a patient in whom there was complete disappearance of such a tumor following regional hyperthermia and chemotherapy.
Advanced uterine leiomyosarcoma (LMS) is a rare and extremely aggressive disease. In patients with advanced and unresected uterine LMS, multidisciplinary therapy is the best treatment option, although no consensus exists on the efficacy of the treatment. The present study describes the case of a

Leiomyosarcoma of the small intestine presenting as fever of unknown origin.

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We report a patient with a jejunal leiomyosarcoma who presented with fever of unknown origin. Resection of the tumour resulted in resolution of his symptoms.
Pazopanib-a multitargeted tyrosine kinase inhibitor with prominent antiangiogenic effects-has shown promise in the treatment of soft-tissue sarcomas. Hyperthermia has been also applied as an adjunctive treatment to chemotherapy for these malignancies. Here, we show that pazopanib and hyperthermia

An unusual case of colonic leiomyosarcoma presenting with fever--significant uptake of radioactivity of gallium-67 in the tumor.

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Leiomyosarcoma of the large intestine, excluding the rectum, is a rare lesion and only 58 cases have been previously reported. Significant uptake of radioactivity of gallium-67 to the tumor has not been reported and this report may be the first case. Although preoperative diagnosis is considered to

[Uterine leiomyosarcoma as a cause of fever of unknown origin].

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Pyrexia of unknown origin: a case of uterine leiomyosarcoma.

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Uterine Leiomyosarcoma Presenting with a Fever of Unknown Origin.

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Leiomyosarcoma of the duodenum; report of case with fever and abdominal pain for 7 years.

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Pharyngeal leiomyosarcoma with fever of unknown origin.

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Positive response of a primary leiomyosarcoma of the breast following salvage hyperthermia and pazopanib.

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Uterine leiomyosarcoma with osteoclast like giant cells and long standing systemic symptoms.

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BACKGROUND The leiomyomatous type of uterine sarcoma with osteoclast-type giant cell component is a rare variant of uterine tumors with poor prognosis. The histological diagnosis of these rare tumors can be problematic and only five such tumors have been published previously. METHODS A 54-year-old

[Primary leiomyosarcoma of the liver 37 years after successful treatment of hereditary retinoblastoma].

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In patients successfully treated for hereditary retinoblastoma, the risk of developing a second non-ocular tumor has been reported. We report the first case of primary hepatic leiomyosarcoma in a 39 year-old woman who has been treated 37 years before for hereditary retinoblastoma of the left eye.
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