Figure 2.
Histopathologic and molecular characterization of short telomere MDS/AML. (A) Hypoplastic MDS (MDS with multilineage dysplasia; biopsy [hematoxylin-and-eosin stain (H&E); original magnification ×10]). (B) Multilineage dysplasia involving the myeloid (red arrows), erythroid (green arrow; aspirate [Wright-Giemsa stain; original magnification ×100]) and (C) megakaryocytic (yellow arrows; biopsy [H&E; original magnification ×40]) lineages. (D) MDS (MDS with ring sideroblasts and multilineage dysplasia; biopsy [H&E; original magnification ×10]). (E) Multilineage dysplasia involving the erythroid lineage (green arrows; aspirate [Wright-Giemsa stain; original magnification ×100]) with (F) abundant ring sideroblasts (aspirate [iron stain; original magnification ×100x]). Rare blasts (G, black arrow; Wright-Giemsa stain; original magnification ×100) are seen, and megakaryocytes (H) are also dysplastic (yellow arrows; H&E; original magnification ×40). (I) Hypoplastic AML (AML with myelodysplasia-related changes; biopsy [H&E; original magnification ×10]). Increased blasts (J, ∼70%) with background multilineage dysplasia involving the myeloid (K, red arrows) and erythroid (L, green arrows) lineages (aspirate [Wright-Giemsa stain; original magnification ×100]). (M) Hypoplastic AML (AML with myelodysplasia-related changes; biopsy [H&E; original magnification ×10]). Increased blasts (N; ∼50%) with background multilineage dysplasia involving the myeloid (O, red arrows) and erythroid (P, green arrow) lineages (aspirate [Wright-Giemsa stain; original magnification ×100]). (Q) Pie chart showing the distribution of karyotypes of 18 MDS/AML cases. Monosomy 7 abnormalities are listed on the left. (R) Somatic mutation profile of age-matched short telomere patients separated by those with (9 male/5 female) and without (11 male/9 female) MDS/AML. The age for each patient is included on top as is the presence of a monosomy 7 abnormality [−7, del(7q) or der(1;7)(q10;p10)]. All sequencing was performed on blood, except for the 2 AML cases (denoted as bolded ages) for which bone marrow was used. The ring sideroblasts (defined as >15% of cells examined) are denoted below the MDS/AML cases by an asterisk (*). Of note, another patient (of a total of 7) had ring sideroblasts but was not included in this analysis because of insufficient DNA. The respective germline mutations for each case are annotated in supplemental Figure 1A.

Histopathologic and molecular characterization of short telomere MDS/AML. (A) Hypoplastic MDS (MDS with multilineage dysplasia; biopsy [hematoxylin-and-eosin stain (H&E); original magnification ×10]). (B) Multilineage dysplasia involving the myeloid (red arrows), erythroid (green arrow; aspirate [Wright-Giemsa stain; original magnification ×100]) and (C) megakaryocytic (yellow arrows; biopsy [H&E; original magnification ×40]) lineages. (D) MDS (MDS with ring sideroblasts and multilineage dysplasia; biopsy [H&E; original magnification ×10]). (E) Multilineage dysplasia involving the erythroid lineage (green arrows; aspirate [Wright-Giemsa stain; original magnification ×100]) with (F) abundant ring sideroblasts (aspirate [iron stain; original magnification ×100x]). Rare blasts (G, black arrow; Wright-Giemsa stain; original magnification ×100) are seen, and megakaryocytes (H) are also dysplastic (yellow arrows; H&E; original magnification ×40). (I) Hypoplastic AML (AML with myelodysplasia-related changes; biopsy [H&E; original magnification ×10]). Increased blasts (J, ∼70%) with background multilineage dysplasia involving the myeloid (K, red arrows) and erythroid (L, green arrows) lineages (aspirate [Wright-Giemsa stain; original magnification ×100]). (M) Hypoplastic AML (AML with myelodysplasia-related changes; biopsy [H&E; original magnification ×10]). Increased blasts (N; ∼50%) with background multilineage dysplasia involving the myeloid (O, red arrows) and erythroid (P, green arrow) lineages (aspirate [Wright-Giemsa stain; original magnification ×100]). (Q) Pie chart showing the distribution of karyotypes of 18 MDS/AML cases. Monosomy 7 abnormalities are listed on the left. (R) Somatic mutation profile of age-matched short telomere patients separated by those with (9 male/5 female) and without (11 male/9 female) MDS/AML. The age for each patient is included on top as is the presence of a monosomy 7 abnormality [−7, del(7q) or der(1;7)(q10;p10)]. All sequencing was performed on blood, except for the 2 AML cases (denoted as bolded ages) for which bone marrow was used. The ring sideroblasts (defined as >15% of cells examined) are denoted below the MDS/AML cases by an asterisk (*). Of note, another patient (of a total of 7) had ring sideroblasts but was not included in this analysis because of insufficient DNA. The respective germline mutations for each case are annotated in supplemental Figure 1A.

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