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10  Blood Vessels  251

             Q. Classify vascular tumours.

             Ans.  Classification
               1.  Benign neoplasms, developmental and acquired conditions
                 (a)  Haemangioma
                     (i)  Capillary haemangioma
                    (ii)  Cavernous haemangioma
                     (iii)  Pyogenic granuloma
                 (b)  Lymphangioma
                     (i)  Simple (capillary lymphangioma)
                    (ii)  Cavernous lymphangioma (cystic lymphangioma)
                 (c)  Glomus tumour
                  (d)  Vascular ectasias
                     (i)  Nevus flammeus
                    (ii)  Spider telangiectasia (arterial spider)
                     (iii)  Hereditary haemorrhagic telangiectasia (Osler–Weber–Rendu disease)
                 (e)  Reactive vascular proliferations
                   Bacillary angiomatosis
               2.  Intermediate grade neoplasms
                 (a)  Kaposi sarcoma
                 (b)  Hemangioendothelioma
               3.  Malignant neoplasms
                 (a)  Angiosarcoma
                 (b)  Hemangiopericytoma

             Q. Describe the clinicopathological features of haemangiomas.

             Ans.  Haemangiomas are common benign tumours of infancy and childhood. These are
             difficult to differentiate from malformations or hamartomas.
               May be         Localized (angiomas)
                             Diffuse (angiomatosis; involve large segments of the body, eg,
                             entire extremity)
               May be        Superficial (head and neck)
                             Internal or visceral (liver)

               1.  Capillary haemangioma
                 (a)  Largest single type of vascular tumour believed to be a proliferation of vascular
                   endothelial cells. It is composed of capillary channels with RBCs.
                 (b)  Most commonly found in the skin, subcutaneous tissue and mucous membranes
                   of the oral cavities and lips; presents as a red to reddish-purple raised lesion. May
                   also be seen in the liver, spleen and kidneys.
                 (c)  ‘Strawberry type’ of capillary haemangioma is very common and tends to regress
                   by seven years of age in 75–90% cases.
                  (d)  Capillary haemangioma may cause cosmetic disturbance or manifest with bleeding
                   due to traumatic ulceration.
               2.  Pyogenic  granuloma  (lobular  capillary  haemangioma  or  polypoid  capillary
                haemangioma)
                 (a)  Typically presents as a red/pink to purple nodule, smooth or lobulated, which may
                   follow trauma.
                 (b)  Shows a striking resemblance to exuberant granulation tissue with oedema and
                   acute and chronic inflammation.
                 (c)  ‘Granuloma  gravidarum’  is  a  pyogenic  granuloma  occurring  in  10%  of  the
                   pregnant women (regresses after delivery).
               3.  Cavernous haemangioma
                 (a)  Usually involves deeper structures
                 (b)  Locally destructive large lesions, which show no tendency to regress
                 (c)  Red-blue, soft, spongy 1–2 cm in diameter
                  (d)  Rare giant forms that affect large subcutaneous areas of face or extremities



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