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Splenic solid lesions
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== '''Benign''' == * '''Inflammatory''' ** '''Sarcoidosis''' * '''Congenital''' ** '''Lymphangioma''' *** Rare, benign, slow-growing *** Mainly seen in childhood *** Endothelium-lined cysts *** Present as splenomegaly secondary to cyst enlargement *** Lymphangiosarcoma can be found within the lesion *** Splenectomy appropriate ** '''Primary cyst''' * '''Acquired''' ** '''False cyst''' ** '''Infarction''' * '''Vascular''' ** '''Haemangioma''' *** Most common *** Usually incidental *** Usually solitary *** Mostly <2cm (larger lesions associated with rupture) *** Can be classified as either cavernous haemagioma or capillary haemangioma ** '''Hamartoma''' *** Malformed splenic red pulp elements without organised lymphoid follicles *** Usually <3cm *** Spontaneous rupture has been described, but mostly not *** Frequently splenectomy is necessary for a definitive diagnosis ** '''Littoral cell angioma''' *** Multiple nodular masses leading to splenomegaly and hypersplenism *** Usually seen as multiple masses of varying sizes that isodense on noncon CT, hypodense on early portal phase, isodense an delayed phase ** '''Sclerosing angiomatous nodular transformation (SANT)''' * '''Infectious''' ** '''Pyogenic abscess''' ** '''Fungal abscess''' ** '''Tuberculosis''' ** '''Hydatid cyst''' == '''Malignant''' == * '''Lymphoma''' ** See section on 'splenectomy for haematologic diseases' * '''Angiosarcoma''' ** Highly aggressive, poor prognosis ** Splenomegaly is common, and spontaneous rupture occurs in up to 25% ** Liver mets commonly found at presentation ** Can also present with haemolytic anaemia, ascites, or pleural effusions ** Linked with environmental exposures - thorium dioxide and monomeric vinyl chloride * '''Haemangiopericytoma''' * '''Splenic metastasis''' ** Most commonly '''melanoma, breast, lung''' ** Can also see '''ovarian''', and rarely '''pancreatic, colon, stomach''' ** Radiological appearance variable ** Can see implants in serosal surface in '''peritoneal carcinomatosis''' ** Splenectomy can provide palliation of splenomegaly symptoms and prevent rupture, for carefully-chosen patients ** (relatively uncommon, maybe because of a lack of afferent lymphatics, but are found in up to 7% of cancer patients at autopsy) == '''Indeterminate''' == * '''Inflammatory pseudotumour (inflammatory myofibroblastic tumour)''' ** Uncertain aetiology ** Mainly incidental ** Spindle cell proliferation admixed with abundant inflammatory cells ** Most cases >10cm in diameter ** CT: hypodense mass with delayed enhancement, with a central scar without enhancement ** Final diagnosis usually made after splenectomy [[Category:Spleen]]
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