A Cavrnous Hemangioma is an abnormal tangle of tightly packed thin walled capillaries that are probe to bleeding.

Beckwith-Wiedemann Syndrome (BWS) is associated with early development of embryonal tumours usually in the first four years of life. We describe a patient who presented with a right adrenal cyst in the first month of life and hepatoblastoma in the third month of life. A cavernous haemangioma was subsequently found in the resected tumour.

Hepatic angiosarcoma is a rare primary mesenchymal malignancy. Prognosis is poor and mortality occurs early. The diagnosis is challenging. Our case was an asymptomatic 70 year-old man referred, with incidental ultrasonography finding of multiple liver nodules. Diagnostic laparoscopic liver biopsy and the histopathological examination reported a haemangioma. Six months later, he became symptomat...

An infant presenting with high-output cardiac failure and a single large diffuse haemangioma of the liver is described. Corticosteroid therapy failed to produce any improvement, but hepatic artery ligation was followed by dramatic disappearance of the signs of cardiac failure and a decrease in the size of the liver without any evidence of lasting liver damage.

This report concerns the case of an unusual tumour of the epididymis, i.e. a haemangioma. This led to secondary extensive bleeding and haemorrhagic infarcting of the testis and the epididymis. Frequency, diagnosis, differential diagnosis, therapy and prognosis of the tumours of the epididymis are also discussed.

Intramuscular haemangiomas (IMHs) are rare benign vascular neoplasms that account for approximately 0.8% of all haemangiomas. The histology of IMHs can reveal cavernous dilated spaces. We report an interesting case of haemangioma in the deep skeletal muscle of the right labial mucosa in a young man involving the orbicularis oris muscle which showed additional features of sinusoidal arrangement ...

Journal of Cutaneous and Aesthetic Surgery ¦ Volume 10 ¦ Issue 2 ¦ April‐June 2017 114 characteristic moat‐like collarette of skin surrounding its base. Histopathologically, it shows fibrovascular proliferation in the dermis with an overlying hyperkeratotic and acanthotic epidermis.[10] Thus lobular capillary haemangioma or pyogenic granuloma should be considered in the differential diagnosis o...

An 8-week-old infant was treated with oral propranolol for a haemangioma of infancy. The standard dose (according to protocol) is 2 mg/kg/day but, because of a mistake by the pharmacist, the child was treated with 8 mg/kg/day without any side effects (pulse, blood pressure and glucose stayed normal).