Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report

<p>Abstract</p> <p>Introduction</p> <p>Many fetal malformations can occur because of maternal diabetes. However, ambiguous genital organs have never been reported as an associated finding in the literature. This is the first report of associated ambiguous genital organ...

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Main Authors: Tantbirojn Patou, Taweevisit Mana, Sritippayawan Suchila, Uerpairojkit Boonchai
Format: Article
Language:English
Published: BMC 2008-07-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/2/1/251
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spelling doaj-0c372b48650f4297b71cb887840525622020-11-24T22:06:27ZengBMCJournal of Medical Case Reports1752-19472008-07-012125110.1186/1752-1947-2-251Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case reportTantbirojn PatouTaweevisit ManaSritippayawan SuchilaUerpairojkit Boonchai<p>Abstract</p> <p>Introduction</p> <p>Many fetal malformations can occur because of maternal diabetes. However, ambiguous genital organs have never been reported as an associated finding in the literature. This is the first report of associated ambiguous genital organ and bilateral adrenal hyperplasia in a case of diabetic fetopathy.</p> <p>Case presentation</p> <p>A 19-year-old Thai primigravida with familial history of diabetes mellitus (DM) was diagnosed as having gestational DM type 2, based on 100 g oral glucose tolerance test, and was poorly controlled with insulin injections. Delayed targeted ultrasonography at 28 weeks gestation revealed multiple fetal anomalies. The woman underwent low transverse cesarean section at 30 weeks gestation due to preterm labor and transverse lie. The newborn with ambiguous genitalia was delivered but expired after birth. Autopsy findings revealed alobar holoprosencephaly, a prominent forehead, hypotelorism, an absent nose, absent bilateral ears, median cleft lip and palate, preaxial polydactyly of the right hand, accessory spleens, single umbilical artery, markedly enlarged adrenal glands and ambiguous external genitalia The subsequent fetal chromosomal study revealed 46,XX.</p> <p>Conclusion</p> <p>We describe a case of diabetic fetopathy with classic facial malformation and preaxial hallucal polydactyly which has been proposed as a marker of diabetic embryopathy. Bilateral adrenal hyperplasia with ambiguous genitalia, an uncommon associated anomaly, was also identified. It is controversial whether adrenal hyperplasia can be a novel feature of diabetic fetopathy or just a coincidental finding. Further observation and adequate investigation are needed in such cases.</p> http://www.jmedicalcasereports.com/content/2/1/251
collection DOAJ
language English
format Article
sources DOAJ
author Tantbirojn Patou
Taweevisit Mana
Sritippayawan Suchila
Uerpairojkit Boonchai
spellingShingle Tantbirojn Patou
Taweevisit Mana
Sritippayawan Suchila
Uerpairojkit Boonchai
Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
Journal of Medical Case Reports
author_facet Tantbirojn Patou
Taweevisit Mana
Sritippayawan Suchila
Uerpairojkit Boonchai
author_sort Tantbirojn Patou
title Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
title_short Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
title_full Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
title_fullStr Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
title_full_unstemmed Diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
title_sort diabetic fetopathy associated with bilateral adrenal hyperplasia and ambiguous genitalia: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2008-07-01
description <p>Abstract</p> <p>Introduction</p> <p>Many fetal malformations can occur because of maternal diabetes. However, ambiguous genital organs have never been reported as an associated finding in the literature. This is the first report of associated ambiguous genital organ and bilateral adrenal hyperplasia in a case of diabetic fetopathy.</p> <p>Case presentation</p> <p>A 19-year-old Thai primigravida with familial history of diabetes mellitus (DM) was diagnosed as having gestational DM type 2, based on 100 g oral glucose tolerance test, and was poorly controlled with insulin injections. Delayed targeted ultrasonography at 28 weeks gestation revealed multiple fetal anomalies. The woman underwent low transverse cesarean section at 30 weeks gestation due to preterm labor and transverse lie. The newborn with ambiguous genitalia was delivered but expired after birth. Autopsy findings revealed alobar holoprosencephaly, a prominent forehead, hypotelorism, an absent nose, absent bilateral ears, median cleft lip and palate, preaxial polydactyly of the right hand, accessory spleens, single umbilical artery, markedly enlarged adrenal glands and ambiguous external genitalia The subsequent fetal chromosomal study revealed 46,XX.</p> <p>Conclusion</p> <p>We describe a case of diabetic fetopathy with classic facial malformation and preaxial hallucal polydactyly which has been proposed as a marker of diabetic embryopathy. Bilateral adrenal hyperplasia with ambiguous genitalia, an uncommon associated anomaly, was also identified. It is controversial whether adrenal hyperplasia can be a novel feature of diabetic fetopathy or just a coincidental finding. Further observation and adequate investigation are needed in such cases.</p>
url http://www.jmedicalcasereports.com/content/2/1/251
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