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1.
Transfusion ; 64(1): 189-193, 2024 01.
Artigo em Inglês | MEDLINE | ID: mdl-38031483

RESUMO

INTRODUCTION: Hereditary pyropoikilocytosis (HPP) is a heterogeneous inherited disorder of red blood cell (RBC) membrane and cytoskeletal proteins that leads to hemolytic anemia. HPP is characterized by marked poikilocytosis, microspherocytes, RBC fragmentation, and elliptocytes on peripheral blood smear. Mutations in SPTA1 can cause HPP due to a quantitative defect in α-spectrin and can lead to profound fetal anemia and nonimmune hydrops fetalis, which can be managed with intrauterine transfusion. CASE PRESENTATION: We present a case of a 26-year-old G4P2102 woman of Amish-Mennonite ancestry with a pregnancy complicated by fetal homozygosity for an SPTA1 gene variant (SPTA1c.6154delG) as well as severe fetal anemia and hydrops fetalis, which was managed with four intrauterine transfusions between 26 and 30 weeks gestation. Pre-transfusion peripheral smears from fetal blood samples showed RBC morphology consistent with HPP. The neonate had severe hyperbilirubinemia at birth, which has resolved, but remains transfusion-dependent at 6 months of life. DISCUSSION/CONCLUSION: To our knowledge, this is the first report that correlates homozygosity of the SPTA1c.6154delG gene variant with RBC dysmorphology and establishes the diagnosis of HPP.


Assuntos
Anemia Hemolítica , Eliptocitose Hereditária , Doenças Fetais , Doenças Hematológicas , Gravidez , Feminino , Recém-Nascido , Humanos , Adulto , Hidropisia Fetal/diagnóstico , Hidropisia Fetal/genética , Hidropisia Fetal/terapia , Eliptocitose Hereditária/complicações , Eliptocitose Hereditária/diagnóstico , Eliptocitose Hereditária/genética , Proteínas do Citoesqueleto , Anemia Hemolítica/complicações
2.
Fetal Pediatr Pathol ; 43(3): 273-275, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38108326

RESUMO

Background: The available literature on intrauterine transfusion focuses largely on its application in fetal alloimmunization rather than hereditary red cell disorders, with limited illustration of its associated histopathologic findings. Case report: We present the histologic findings in a placenta associated with preterm delivery of an infant with autosomal SPTA1 mutation following multiple intrauterine transfusions, including appropriate villous maturation, subchorionic organizing hematomas, hemosiderin-laden macrophages, and dysmorphic fetal erythrocytes within villous capillaries. Conclusion: Intrauterine transfusion is associated with placental histologic findings that reflect procedural changes without significant disruption of placental membranes or villous maturation.


Assuntos
Transfusão de Sangue Intrauterina , Placenta , Humanos , Feminino , Gravidez , Transfusão de Sangue Intrauterina/métodos , Placenta/patologia , Recém-Nascido , Adulto , Eliptocitose Hereditária/genética , Eliptocitose Hereditária/patologia , Eliptocitose Hereditária/diagnóstico , Doenças Fetais/patologia
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