“…3 Further immunohistochemical staining, such as with PROX-1, D2-40, ERG, CD31 or CD34 can confirm the presence of these lymphatic endothelial cells. 7,9,10 This is distinct from kaposiform haemangioendothelioma (KHE), another disorder associated with abnormal lymphatic channels and spindled cells, however the histological architecture is of more defined solid confluent tumour, often with microthombi. 3 Clinically, KHE differs further as the lesions are typically unifocal vascular tumours presenting in infancy, which may involve skin and soft tissues, retroperitoneum or viscera, 3 with larger lesions commonly associated with thrombocytopenia resulting in consumptive coagulopathy (KasabacheMerritt phenomenon).…”