Aplastic anemia (AA) is an acquired bone marrow failure (BMF) disorder characterized by hypocellular bone marrow and pancytopenia. The pathogenic mechanism is an immune-mediated attack against hematopoietic precursors, and the concomitant detection of a paroxysmal nocturnal hemoglobinuria (PNH) clone, or its emergence over time, is a frequent event. Pregnancy is one of the proposed risk factors for autoimmune disease development and cases of AA in pregnant women were described in numerous case series. [1][2][3][4][5] However, limited data are available on the management of BMFs during pregnancy or on feto-maternal outcomes.We conducted a single-center retrospective cohort study including women with acquired AA and/or PNH, referred to a tertiary center in the United Kingdom over the last 25 years. The study focused on women who experienced either a relapse of known AA or a de novo occurrence of BMF during pregnancy. Demographic, clinical, and disease severity findings according to Camitta criteria 6 were collected.Additionally, information regarding treatment administered before, during, and after each pregnancy, response to AA-treatment, according to RACE trial adopted criteria, 7 as well as feto-maternal outcomes were systematically recorded.Seventy pregnancies occurring in 52 women were included from a cohort of 266 women with BMF followed from 1989 until 2022; 17 patients developed AA de novo during pregnancy, while 28 had a diagnosis of AA predating pregnancy (Table S1). Additionally, seven patients had a hemolytic PNH (two with onset during pregnancy and five with a previous diagnosis).Regarding 17 de novo AA, most presented during the first trimester, 57% versus 36% and 7% in the second and third trimester respectively, with severe presentation in 29% of cases. In seven patients a PNH clone was detected with a median granulocytes clone of 5.2%(1.7-19). During pregnancy, 16 (94%) required blood transfusions and eight (47%) immunosuppressive therapy (IST) with cyclosporin (CSA) (five patients, three responsive) or steroids (three subjects, one responsive). After delivery, spontaneous hematologic improvement occurred in seven subjects (41%), however, 10 (59%) required IST or transplant (5 ATG + CSA ± Eltrombopag; 4 CSA/Androgens; 1 HSCT) all with response. Maternal adverse events (AEs) were observed in 29% of pregnancies, including two peripartum bleedings, one preterm premature rupture of the membrane (PPROM), and a Cesarean scar infection. Three women needed an urgent Cesarean Section (CS) (one for PPROM, two unknown), and three received additional peripartum transfusion support. No spontaneous miscarriages occurred, but fetal