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    Cerebrotendinous xanthomatosis
    (2001) Ekşioğlu F.; Güdemez E.; Bozdoğan Ö.; Altinok D.; Ulkatan S.
    Cerebrotendinous xanthomatosis is a rare metabolic disease of autosomal recessive inheritance. Clinical findings include tendon xanthoma, cataract, neurological dysfunction, ataxia, dementia, slightly high serum cholesterol levels. We report a case aged 17 had painless, semimobile, solid masses on her both achilles tendon diagnosed as cerebrotendinous xanthomatosis. Cerebrotendinous xanthomatosis must be considered in the diagnosis of patients with tendon xanthoma, cataract, neurological dysfunction, ataxia, dementia, slightly high serum cholesterol levels.
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    Öğe
    Diffuse plane xanthomatosis in a patient with Budd-Chiari syndrome and monoclonal gammopathy
    (2009) Koçak M.; Keleş H.; Yakaryilmaz F.; Bozdoğan Ö.; Güliter S.
    Diffuse plane xanthomas are characterized by the presence of yellowish plaques on the eyelids, neck, upper trunk, buttocks, and flexural folds. Histology shows foamy histiocytes in the dermis. Approximately half of the cases are associated with lymphoproliferative disorders. Budd-Chiari syndrome is an uncommon condition induced by thrombotic or nonthrombotic obstruction of hepatic venous outflow. We present a case of diffuse plane xanthoma in a 62-year-old man who developed normolipemic plane xanthomas coinciding with Budd-Chiari syndrome and monoclonal gammopathy. We review the English-language literature regarding the rare association of xanthomas and Budd-Chiari syndrome.