Autoimmune Hemolytic Anemia as a Paraneoplastic Syndrome
Abstract: Paraneoplastic autoimmune hemolytic anemia is a rare syndrome. It has been mostly recognized in association with lymphoproliferative disorders and to a much lesser extent in association with solid organ tumors. It has been reported in cases of breast, ovarian, prostate, thymic and renal cancer. The onset and severity is variable. Although it is rare, but should be considered in the differential diagnosis of anemia in patients with malignancy. Keeping high suspicion index is key to diagnosis. It resolves with tumor eradication or excision. Recurrence of hemolysis after a period of cancer remission could point towards relapse.
Keywords: autoimmune hemolytic anemia, solid tumor, paraneoplastic syndrome
How to Cite?: Hala Aziz, Ali Al-Adhami, "Autoimmune Hemolytic Anemia as a Paraneoplastic Syndrome", Volume 7 Issue 2, February 2018, International Journal of Science and Research (IJSR), Pages: 700-701, https://www.ijsr.net/getabstract.php?paperid=ART2018119, DOI: https://dx.doi.org/10.21275/ART2018119