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P. Saint-Blancard, K. Hardy, A. Bonnichon, et al., “Three-Year Survival after Treatment of a Primary Pulmonary Angiosarcoma,” Revue de Pneumologie Clinique, Vol. 63, No. 1, 2007, pp. 55-58.

has been cited by the following article:

• TITLE: Metastatic Primary Pulmonary Angiosarcoma

  AUTHORS: Brendan F. Judy, Jarrod D. Predina, Jay Mittal, Charuhas Deshpande, Sunil Singhal

  KEYWORDS: Angiosarcoma; Pulmonary; Tumor; Surgery

  JOURNAL NAME: Surgical Science, Vol.2 No.3, May 18, 2011

  ABSTRACT: Angiosarcoma is an extremely aggressive tumor with a high rate of mortality. It can arise in any tissue of the body and is most commonly found in the skin and soft tissue[1]. Pulmonary angiosarcoma is usually secondary to a primary location of the body and presents as both solitary and multiple nodules. Primary pulmonary angiosarcoma is a rare disease with less than 20 cases reported in the English literature. In our report we present a case of metastatic primary pulmonary angiosarcoma involving the most ( > 100) pulmonary nodules known to date. Novel treatment strategy using an anti-angiogenic inhibitor was used to treat this disease for the first time to our knowledge; however, it was unsuccessful in controlling disease progression. This report reviews the literature of this rare and devastating disease.