Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report.

Maisonneuve, Emeline; Sohier Lepine, Marlène; Maurice, Paul; Pissard, Serge; Lafon, Bertrand; Mailloux, Agnès; Dhombres, Ferdinand; Leverger, Guy; Jouannic, Jean-Marie (2023). Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report. Transfusion, 63(1), pp. 257-262. Wiley-Blackwell 10.1111/trf.17177

[img]
Preview
Text
Maisonneuve_Transfusion_2022_AAM.pdf.pdf - Accepted Version
Available under License Publisher holds Copyright.

Download (360kB) | Preview
[img] Text
Maisonneuve_Transfusion_2023.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.

Download (602kB)

BACKGROUND

Pyruvate Kinase (PK) deficiency is the most common enzyme defect of glycolysis, leading to congenital hemolytic anemia, which can occur during the neonatal period.

STUDY DESIGN AND METHODS

We report the prenatal management of fetal anemia related to PK deficiency in a family with a severe proband.

RESULTS

The couple had a first child born with hydrops, whose PK deficiency was diagnosed at 18 months of life. He was treated with allogeneic bone marrow transplantation. The second child was free from disease. For the third pregnancy, the amniocentesis revealed a PK deficiency. Weekly ultrasound monitoring of the middle cerebral artery velocity allowed the detection of severe fetal anemia. Two intrauterine red blood cell transfusions (IUTs) were performed, raising the fetal hemoglobin from 6.6 to 14.5 g/dl at 28 weeks' gestation and from 8.9 to 15.3 g/dl at 31 weeks. A hematopoietic stem cell allograft was discussed prenatally but not chosen, as it would not have significantly changed the perinatal prognosis. The patient delivered a 2730 g girl at 37 weeks, with hemoglobin of 13.6 g/dl. The child presented with neonatal jaundice treated with phototherapy and received postnatal transfusions.

DISCUSSION

When a proband is identified in a family, fetal investigation is warranted, to set up third-trimester ultrasound surveillance and perinatal management. In case of fetal severe anemia of unknown etiology, the workup on fetal blood sampling before IUT should comprise the search for erythrocytes enzymopathies, such as PK deficiency. IUTs allow safer full-term delivery in cases with PK deficiency.

Item Type:

Journal Article (Further Contribution)

Division/Institute:

04 Faculty of Medicine > Medical Education > Institute of General Practice and Primary Care (BIHAM)

UniBE Contributor:

Maisonneuve, Emeline Louise Jacqueline

Subjects:

600 Technology > 610 Medicine & health
300 Social sciences, sociology & anthropology > 360 Social problems & social services

ISSN:

0041-1132

Publisher:

Wiley-Blackwell

Language:

English

Submitter:

Doris Kopp Heim

Date Deposited:

16 Nov 2022 09:38

Last Modified:

10 Nov 2023 00:25

Publisher DOI:

10.1111/trf.17177

PubMed ID:

36349479

Uncontrolled Keywords:

congenital hemolytic anemia hematopoietic stem cell transplantation intrauterine transfusion pregnancy prenatal diagnosis pyruvate kinase deficiency

BORIS DOI:

10.48350/174812

URI:

https://boris.unibe.ch/id/eprint/174812

Actions (login required)

Edit item Edit item
Provide Feedback