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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Synchronously diagnosed eosinophilic granuloma and Hodgkin's disease in a 12-year-old boy: a case report | Journal of Medical Case Reports BioMed Central Open Access Case report Synchronously diagnosed eosinophilic granuloma and Hodgkin s disease in a 12-year-old boy a case report Soheila Sarmadi1 Amir B Heidari 2 Amir H Sina1 and Mohammad A Ehsani3 Address 1Pathology Department Bahrami Children s Hospital Tehran University of Medical Sciences Tehran Iran 2Pathology Department Medical Faculty Tehran University of Medical Sciences Tehran Iran and 3Hematology and Oncology Department Bahrami Children s Hospital Tehran University of Medical Sciences Tehran Iran Email Soheila Sarmadi - ssarmadi@sina.tums.ac.ir Amir B Heidari - amirbehzad@yahoo.com Amir H Sina - amirhoseinsina@yahoo.com Mohammad A Ehsani - mohamadali.ehsani@yahoo.com Corresponding author Published 29 January 2009 Received 4 March 2008 Journal of Medical Case Reports 2009 3 35 doi 10.1186 1752-1947-3-35 Accepted 29 January 2009 This article is available from http www.jmedicalcasereports.cOm content 3 1 35 2009 Sarmadi 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 Synchronous composite tumors are uncommon. Simultaneous rather than metachronous or consecutive occurrences of eosinophilic granuloma and Hodgkin s lymphoma in children are very rare. This is the first report of this kind in the medical literature. Case presentation We report the case of a 12-year-old Iranian boy with eosinophilic granuloma localized in his leg around the knee and Hodgkin s lymphoma in a cervical lymph node. The two tumours occurred synchronously before the patient had received any treatment. Conclusion Several cases of an association between eosinophilic granuloma and .
