A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization

Background. Aplasia cutis congenita (ACC) is a rare congenital localized skin defect that is mostly diagnosed in the newborn or infant period. ACC type 5 often involves the trunk or extremities accompanied by fetus papyraceous (FP) or placental infarcts. The etiology and pathogenesis of this...

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Main Authors: Sae Yun Kim, Eun Sun Kim, Joonhong Min, Kyungyul Lee
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2022-02-01
Series:The Turkish Journal of Pediatrics
Subjects:
Online Access:https://turkjpediatr.org/article/view/137
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author Sae Yun Kim
Eun Sun Kim
Joonhong Min
Kyungyul Lee
author_facet Sae Yun Kim
Eun Sun Kim
Joonhong Min
Kyungyul Lee
author_sort Sae Yun Kim
collection DOAJ
description Background. Aplasia cutis congenita (ACC) is a rare congenital localized skin defect that is mostly diagnosed in the newborn or infant period. ACC type 5 often involves the trunk or extremities accompanied by fetus papyraceous (FP) or placental infarcts. The etiology and pathogenesis of this rare type of ACC are not well known. In this case, we report an ACC type 5 with a definite etiology. Case. We report a preterm infant with ACC type 5, with diffuse bilateral leg lesions found at birth. He was the first baby of dichorionic twin after reduction from a dichorionic triplet pregnancy conceived through in vitro fertilization. A fetus papyraceous was found in juxtaposition with the affected baby`s placenta. After 37 days of hospitalization, his leg lesions were successfully epithelized with supportive care. He is regularly visiting the Dermatology clinic for scar care and shows normal development without motor limitation. Conclusions. Herein, we present a preterm infant with ACC type 5 and the placental pathology with fetus papyraceous of the artificially reduced monochorionic co-twin of the affected infant. We suggest a precautious decision in multifetal pregnancy reduction (MFPR) in dichorionic triplets, presenting ACC type 5 as an adverse outcome of MFPR.
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spelling doaj-art-4df2fb99e70b422e89ef64595d6e83c22025-08-20T03:01:10ZengHacettepe University Institute of Child HealthThe Turkish Journal of Pediatrics0041-43012791-64212022-02-0164110.24953/turkjped.2020.1787A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilizationSae Yun Kim0Eun Sun Kim1Joonhong Min2Kyungyul Lee3Department of Pediatrics, Yeouido St. Mary's Hospital, The Catholic University of Korea, Seoul, Korea.Departments of Pediatrics, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, Korea.Departments of Dermatology, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, Korea.Departments of Pathology, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, Korea. Background. Aplasia cutis congenita (ACC) is a rare congenital localized skin defect that is mostly diagnosed in the newborn or infant period. ACC type 5 often involves the trunk or extremities accompanied by fetus papyraceous (FP) or placental infarcts. The etiology and pathogenesis of this rare type of ACC are not well known. In this case, we report an ACC type 5 with a definite etiology. Case. We report a preterm infant with ACC type 5, with diffuse bilateral leg lesions found at birth. He was the first baby of dichorionic twin after reduction from a dichorionic triplet pregnancy conceived through in vitro fertilization. A fetus papyraceous was found in juxtaposition with the affected baby`s placenta. After 37 days of hospitalization, his leg lesions were successfully epithelized with supportive care. He is regularly visiting the Dermatology clinic for scar care and shows normal development without motor limitation. Conclusions. Herein, we present a preterm infant with ACC type 5 and the placental pathology with fetus papyraceous of the artificially reduced monochorionic co-twin of the affected infant. We suggest a precautious decision in multifetal pregnancy reduction (MFPR) in dichorionic triplets, presenting ACC type 5 as an adverse outcome of MFPR. https://turkjpediatr.org/article/view/137aplasia cutis congenitafetus papyraceousin vitro fertilizationmultifetal pregnancy reduction
spellingShingle Sae Yun Kim
Eun Sun Kim
Joonhong Min
Kyungyul Lee
A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
The Turkish Journal of Pediatrics
aplasia cutis congenita
fetus papyraceous
in vitro fertilization
multifetal pregnancy reduction
title A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
title_full A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
title_fullStr A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
title_full_unstemmed A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
title_short A case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
title_sort case of aplasia cutis congenita following fetal reduction of triplet pregnancy conceived through in vitro fertilization
topic aplasia cutis congenita
fetus papyraceous
in vitro fertilization
multifetal pregnancy reduction
url https://turkjpediatr.org/article/view/137
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