Boulay V, Jeanfaivre T, Enon B, Saint-André J P, Tuchais E
Service de Pneumologie, Centre Hospitalier et Universitaire, Angers.
Rev Pneumol Clin. 1998 Oct;54(5):259-62.
Angiosarcoma is an uncommon tumor accounting for approximately 1% of all soft tissue tumors which, themselves account for 0.7% of all malignant tumors. Thoracic parietal localizations are reported exceptionally and prognosis is poor. We report the case of a 79-year-old woman who developed an angiosarcoma of the thoracic wall. The inaugural symptom was a hemothorax. Besides the localization, this case was particularly exceptional since the patient has remained asymptomatic three years after treatment by wide resection followed by radiotherapy.
血管肉瘤是一种罕见的肿瘤,约占所有软组织肿瘤的1%,而软组织肿瘤本身占所有恶性肿瘤的0.7%。胸壁局部受累的情况极为罕见,且预后较差。我们报告一例79岁女性发生胸壁血管肉瘤的病例。首发症状为血胸。除了病变部位外,该病例尤为特殊,因为患者在接受广泛切除并放疗后的三年里一直无症状。