EditorArteriovenous haemangioma (AVH) is a rare, benign, acquired vascular lesion, usually presenting as a solitary bluish asymptomatic papule on the head or extremities. 1 The pathogenesis of AVH is unknown, but it may represent multicentric hamartomatous proliferation of the suprapapillary vascular plexus. Recently, several cases of AVH associated with chronic liver diseases have been described. [2][3][4] We report here a case of AVH in a 57-year-old man with liver cirrhosis and hepatocellular carcinoma associated with chronic hepatitis B. Immunohistochemical analysis showed that the endothelial cells in the tumour were negative for oestrogen receptor. To our knowledge, this is the first report describing oestrogen receptor status of AVH in a patient with chronic liver disease.A 57-year-old Korean man presented at the dermatology unit with a solitary, asymptomatic, progressively enlarging, violaceous nodule of 3 years' duration on his left anterior chest. Eight years previously, he had been diagnosed with chronic active hepatitis associated with hepatitis B virus infection. Six months previously, liver cirrhosis and hepatocellular carcinoma were detected by abdominal ultrasound and computed tomography and treated three times by transhepatic arterial chemoembolization. Laboratory findings, including liver function and coagulation tests, were typical of patients with liver cirrhosis.Physical examination showed a solitary, well-demarcated, round, violaceous nodule 7 mm in diameter on the left anterior chest ( fig. 1). Around the nodule were erythematous patches with radiating fine telangiectasias. Histopathological