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Zeighami, Shahryar, Eslahi, Seyed Ali, Hosseini, Mohammad Mehdi, Ariafar, Ali, Pakbaz, Sara, Rastegari, Mohsen, Khazraei, Hajar. (1394). Extramedullary Hematopoiesis in a Man With β-Thalassemia: An Uncommon Cause of an Adrenal Mass. سامانه مدیریت نشریات علمی, 3(2), 0-0. doi: 10.17795/acr-29003
Shahryar Zeighami; Seyed Ali Eslahi; Mohammad Mehdi Hosseini; Ali Ariafar; Sara Pakbaz; Mohsen Rastegari; Hajar Khazraei. "Extramedullary Hematopoiesis in a Man With β-Thalassemia: An Uncommon Cause of an Adrenal Mass". سامانه مدیریت نشریات علمی, 3, 2, 1394, 0-0. doi: 10.17795/acr-29003
Zeighami, Shahryar, Eslahi, Seyed Ali, Hosseini, Mohammad Mehdi, Ariafar, Ali, Pakbaz, Sara, Rastegari, Mohsen, Khazraei, Hajar. (1394). 'Extramedullary Hematopoiesis in a Man With β-Thalassemia: An Uncommon Cause of an Adrenal Mass', سامانه مدیریت نشریات علمی, 3(2), pp. 0-0. doi: 10.17795/acr-29003
Zeighami, Shahryar, Eslahi, Seyed Ali, Hosseini, Mohammad Mehdi, Ariafar, Ali, Pakbaz, Sara, Rastegari, Mohsen, Khazraei, Hajar. Extramedullary Hematopoiesis in a Man With β-Thalassemia: An Uncommon Cause of an Adrenal Mass. سامانه مدیریت نشریات علمی, 1394; 3(2): 0-0. doi: 10.17795/acr-29003

Extramedullary Hematopoiesis in a Man With β-Thalassemia: An Uncommon Cause of an Adrenal Mass

Iranian Journal of Colorectal Research
مقاله 6، دوره 3، شماره 2، شهریور 2015، صفحه 0-0    اصل مقاله (1.07 M)
شناسه دیجیتال (DOI): 10.17795/acr-29003
نویسندگان
Shahryar Zeighami1؛ Seyed Ali Eslahi* ؛ Mohammad Mehdi Hosseini1؛ Ali Ariafar1؛ Sara Pakbaz2؛ Mohsen Rastegari1؛ Hajar Khazraei3
1Department of Urology, Shiraz University of Medical Sciences, Shiraz, IR Iran
2Pathology Department, Shiraz University of Medical Sciences, Shiraz, IR Iran
3Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, IR Iran
چکیده
Introduction Extramedullary hematopoiesis (EMH) commonly occurs in the spleen, liver and lymph nodes. Rare cases of EMH in the adrenal gland have been reported. Case Presentation We report the case of a 33-year-old man from the South of Iran suffering from major β-thalassemia, who underwent open left adrenalectomy and the histopathology revealed EMH. Conclusions In patients in which a history of hematologic disorders exists, careful imaging and hormonal assay should be done to certify a diagnosis of EMH. However, the surgical management becomes inevitable in certain cases.
کلیدواژه‌ها
Extramedullary hematopoiesis؛ Thalassemia؛ Adrenal
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سامانه مدیریت نشریات علمی. قدرت گرفته از سیناوب