Presence of Cervical Vertebral Anomalies with Concomitant Non-Communicating Hydrocephalus and Multicystic Kidney in a Female Fetus: Where VACTERL-H Meets MURCS.
46, XX Disorders of Sex Development
Abnormalities, Multiple
/ diagnosis
Anal Canal
/ abnormalities
Cardiovascular Abnormalities
Congenital Abnormalities
Digestive System Abnormalities
Esophagus
/ abnormalities
Female
Fetus
/ pathology
Genetic Diseases, X-Linked
Heart Defects, Congenital
/ pathology
Humans
Hydrocephalus
/ diagnosis
Kidney
/ abnormalities
Limb Deformities, Congenital
/ diagnosis
Mullerian Ducts
/ abnormalities
Multicystic Dysplastic Kidney
/ complications
Musculoskeletal Abnormalities
Pregnancy
Spine
/ abnormalities
Trachea
/ abnormalities
3D ultrasound
MURCS
VACTERL-H
malformation
prenatal
Journal
Fetal and pediatric pathology
ISSN: 1551-3823
Titre abrégé: Fetal Pediatr Pathol
Pays: England
ID NLM: 101230972
Informations de publication
Date de publication:
Oct 2022
Oct 2022
Historique:
pubmed:
26
10
2021
medline:
28
9
2022
entrez:
25
10
2021
Statut:
ppublish
Résumé
Congenital multisystemic lesions with co-occurrence of non-random malformations, such as VACTERL-H or MURCS association, often pose serious threads to the newborn and still constitute an antenatal diagnostic dilemma. A malformed fetus with VACTERL-H association at 20 gestational weeks had a skin-covered neural tube defect (NTD) of the lower cervical spine, concomitant hydrocephalus, as well as unilateral multicystic dysplastic kidney and the suspicion of mullerian duct anomaly as potentially assigned to MURCS association. We were able to demonstrate how well-defined, standardized volumetric reconstruction of diagnostic views displaying fetal pathology
Sections du résumé
BACKGROUND
UNASSIGNED
Congenital multisystemic lesions with co-occurrence of non-random malformations, such as VACTERL-H or MURCS association, often pose serious threads to the newborn and still constitute an antenatal diagnostic dilemma.
CASE REPORT
UNASSIGNED
A malformed fetus with VACTERL-H association at 20 gestational weeks had a skin-covered neural tube defect (NTD) of the lower cervical spine, concomitant hydrocephalus, as well as unilateral multicystic dysplastic kidney and the suspicion of mullerian duct anomaly as potentially assigned to MURCS association.
DISCUSSION/CONCLUSION
UNASSIGNED
We were able to demonstrate how well-defined, standardized volumetric reconstruction of diagnostic views displaying fetal pathology
Identifiants
pubmed: 34689682
doi: 10.1080/15513815.2021.1994068
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM