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Báo cáo y học: " Scrotal calcinosis due to resorption of cyst walls: a case report"

Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Scrotal calcinosis due to resorption of cyst walls: a case report | Journal of Medical Case Reports BioMed Central Open Access Case report Scrotal calcinosis due to resorption of cyst walls a case report Alper Parlakgumus 1 Emine T Canpolat2 Kenan Caliskan1 Tamer Colakoglu1 Sedat Yildirim1 Ali Ezer1 and Turgut Noyan1 Address Department of General Surgery Faculty of Medicine Baskent University Ankara Turkey and 2Department of Pathology Faculty of Medicine Baskent University Ankara Turkey Email Alper Parlakgumus - aparlakgumus@yahoo.com Emine T Canpolat - tcanpolat@yahoo.com Kenan Caliskan - ken_caliskan@yahoo.com Tamer Colakoglu - tamercolakoglu@yahoo.com Sedat Yildirim - ysedat@hotmail.com Ali Ezer - ezerali@hotmail.com Turgut Noyan - tnoyan@baskent-adn.edu.tr Corresponding author Published 8 December 2008 Received 31 March 2008 Journal of Medical Case Reports 2008 2 375 doi 10.1186 1752-1947-2-375 Accepted 8 December 2008 This article is available from http www.jmedicalcasereports.cOm content 2 1 375 2008 Parlakgumus et al licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License http creativecommons.org licenses by 2.0 which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Abstract__ Introduction Scrotal calcinosis is a rare benign entity defined as the presence of multiple calcified nodules within the scrotal skin. There are controversies about the origin of this entity. In fact it is still debatable whether scrotal calcinosis is an idiopathic growth or dystrophic calcification of dartoic muscles. It is also unclear whether scrotal calcinosis originates from inflammation of epidermal cysts affected by mild to moderate inflammation of mononuclear cells from foreign body granuloma formation followed by resorption of cyst walls or from eccrine epithelial cysts. Case presentation We report a 41-year-old male Turkish