Literature DB >> 14764967

Fetal hemolytic disease due to anti-Rh17 alloimmunization.

Masaya Hirose1, Keiko Nakanishi, Shouji Kaku, Hiroko Moro, Keiko Hodohara, Hirofumi Aotani, Koichi Takebayashi, Yoichi Noda.   

Abstract

OBJECTIVE: To delineate clinical features of a case of fetal hemolytic disease due to anti-Rh17, along with a review of relevant studies published in English and Japanese.
METHODS: We present clinical features of a -D-/-D- phenotype woman with anti-Rh17 alloimmunization during pregnancy. Relevant English literature in the MEDLINE database was reviewed, while Japanese studies were searched in the Japana Centra Revuo Medicina database.
RESULTS: A Japanese -D-/-D- woman with anti-Rh17 (Hro) was treated during pregnancy. Serial ultrasonography, antibody titers, amniocenteses, and cordocenteses were conducted for perinatal management. Amniocentesis results demonstrated a high delta optical density level of 450 in the amniotic fluid, while cordocentesis revealed alloimmunization between the mother and the fetus as well as fetal hemolytic anemia. Blood flow velocity in the middle cerebral artery indicated a rapid development of fetal anemia. The newborn demonstrated severe anemia and hyperbilirubinemia, which were successfully treated with exchange transfusions. Two cases of prenatally diagnosed fetal hemolytic disease due to anti-Rh17 were found published in English and 5 in Japanese.
CONCLUSION: A -D-/-D- phenotype patient with anti-Rh17 was successfully managed during pregnancy and a good outcome for the neonate was achieved. Our results and a review of related literature led to the following suggestions. The first pregnancy in a -D-/-D- woman may be affected, an anamnestic immune response can easily occur during pregnancy, the level of anti-Rh17 titer is indicative of the degree of fetal hemolysis, and appropriate intrauterine intervention is warranted for achievement of a good outcome. Copyright 2004 S. Karger AG, Basel

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Year:  2004        PMID: 14764967     DOI: 10.1159/000075147

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  6 in total

1.  Successful management of fetal hemolytic disease due to strong anti-Rh17 with plasma exchange and intrauterine transfusion in a woman with the D-- phenotype.

Authors:  Kazuya Mimura; Masayuki Endo; Atsushi Takahashi; Yohei Doi; Mikiko Sakuragi; Tomoko Kiyokawa; Hidetoshi Taniguchi; Yasuji Kitabatake; Mika Handa; Takuji Tomimatsu; Yoshiaki Tomiyama; Yoshitaka Isaka; Tadashi Kimura
Journal:  Int J Hematol       Date:  2019-09-19       Impact factor: 2.490

2.  Relationship between previous maternal transfusions and haemolytic disease of the foetus and newborn mediated by non-RhD antibodies.

Authors:  Slavica Dajak; Srđana Culić; Vedran Stefanović; Jelena Lukačević
Journal:  Blood Transfus       Date:  2013-03-05       Impact factor: 3.443

Review 3.  The Outcome of Hemolytic Disease of the Fetus and Newborn Caused by Anti-Rh17 Antibody: Analysis of Three Cases and Review of the Literature.

Authors:  Slavica Dajak; Nina Ipavec; Mia Cuk; Branka Golubic Cepulic; Jela Mratinovic-Mikulandra; Josipa Milardovic; Vedran Stefanovic
Journal:  Transfus Med Hemother       Date:  2019-10-03       Impact factor: 3.747

4.  Successful transfusion care for a patient with the Rhesus -D- phenotype and antibodies against Rh17 and two additional alloantibodies.

Authors:  Karen M K De Vooght; Ayşe Y Demir; Claudia C Folman; Roger E G Schutgens; Wouter W van Solinge; Hans Kemperman
Journal:  Ann Hematol       Date:  2012-06       Impact factor: 3.673

5.  Ethical Issues and Management of Fetal Hemolytic Anemia Caused by Anti-Rh17 in a Multipara with Rare -D- Phenotype.

Authors:  Patrick P Torreiter; Susanne Macher; Eva-Maria Matzhold; Bernhard Resch; Philipp Klaritsch; Günther F Körmöczi; Helene Polin; Leopold Neuhold; Marlies Schönbacher; Peter Schlenke; Thomas Wagner
Journal:  Transfus Med Hemother       Date:  2021-01-05       Impact factor: 3.747

6.  Sensitization to multiple rh antigens by transfusion of random donor platelet concentrates in a -D- phenotype patient.

Authors:  Jae Won Yun; Eun-Suk Kang; Chang-Seok Ki; Kwang Cheol Koh; Dae Won Kim
Journal:  Ann Lab Med       Date:  2012-10-17       Impact factor: 3.464

  6 in total

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