Introduction: Angiosarcomas are uncommon neoplasias, normally located in th
e skin, liver or heart. Primary angiosarcoma of the lung is rare. Case repo
rt: We report on a 41-year-old patient who presented increasing dyspnea. A
10-cm-angiosarcoma of the inferior lobe of the left lung was detected. Afte
r preoperative chemo- and radiotherapy the patient was referred to our clin
ic for surgical intervention. Resection of the inferior lobe of the lung, r
esection of part of the diaphragm, lymphadenectomy and replacement with a V
ypro-II (R) mesh was performed. Histological examination showed a mesenchym
al neoplasia with myxoid tumor tissue, variable cell density and small prol
iferations of vessels. The immunohistochemical analysis confirmed the diagn
osis of an angiosarcoma. The patient was discharged in a good general state
for further ambulatory radiochemotherapy. Discussion: Angiosarcoma of the
lung must always be included in the differential diagnosis of lung nodules
and diffuse infiltrates despite its rare occurrence. Success with neoadjuva
nt therapy has been reported, but radical resection is recommended due to t
he cumulative bad prognosis.