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Hematologic features in myopathy, lactic acidosis, and sideroblastic anemia (MLASA)

Hematologic features in myopathy, lactic acidosis, and sideroblastic anemia (MLASA)
The images show findings on the Wright-Giemsa-stained peripheral blood smear (panel A) and bone marrow aspirate (panels B through E) from a 17-year-old with MLASA due to biallelic mutations of the YARS2 gene. Panels F and G show ring sideroblasts in the bone marrow aspirate, and panel H shows bone marrow normoblasts with numerous vacuoles in a transmission electron micrograph (EM). The arrows in panels A and B point to Pappenheimer bodies in red blood cells. The arrows in panels D and E point to cytoplasmic vacuoles in red blood cell precursors; vacuoles are also present in normoblasts in panels B and C. Refer to UpToDate for details of the causes, evaluation, and treatment of sideroblastic anemias.
Republished with permission of the American Society of Hematology, from: Li G, Hilliard LM. Morphologic features of normoblasts in a case of myopathy, lactic acidosis, and sideroblastic anemia. Blood 2017; 129:1057; permission conveyed through Copyright Clearance Center, Inc. Copyright © 2017.
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