Prenatal and Neonatal Ultrasound and Magnetic Resonance Imaging Diagnosis of Sprengel's Deformity with Unusual Associations.


Journal

Fetal diagnosis and therapy
ISSN: 1421-9964
Titre abrégé: Fetal Diagn Ther
Pays: Switzerland
ID NLM: 9107463

Informations de publication

Date de publication:
2023
Historique:
received: 06 01 2023
accepted: 09 06 2023
medline: 4 10 2023
pubmed: 3 7 2023
entrez: 2 7 2023
Statut: ppublish

Résumé

Sprengel's deformity is a rare congenital anomaly of the shoulder rim. It is the most common congenital anomaly of the shoulder, associated with cosmetic deformity and abnormal shoulder function. Nonsurgical management can be considered for mild cases. Surgical intervention is indicated in moderate to severe cases with the goal of improving cosmetic appearance and function. The best surgical results are obtained in children aged 3-8 years. Correct diagnosis is very important because Sprengel's deformity can be accompanied by additional abnormalities, even in mild cases, and lack of a diagnosis delays proper treatment of the child. The severity of the defect may progress, so it is important to correctly identify children with Sprengel's deformity, even those with a mild form of the defect. We report a case of prenatal sonographic diagnosis of Sprengel's deformity with additional features, as yet undescribed and missed - although visible - on prenatal magnetic resonance imaging (MRI). Cesarean delivery was performed due to preterm rupture of membranes, and a postnatal MRI confirmed the unusual constellation of Sprengel's anomaly with lateral meningocele, vestigial posterior meningocele, and lipoma tethering of the cord to the dural sac at the cervical-thoracic junction. Diagnosis of Sprengel's deformity is possible with prenatal ultrasound. Asymmetry of the cervical spine, discontinuity of the vertebral arch and abnormal vertebral bodies, as well as the asymmetric position of the shoulder blades with the presence of an omovertebral bone are signs that can help diagnose the defect.

Identifiants

pubmed: 37393895
pii: 000531677
doi: 10.1159/000531677
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

269-275

Informations de copyright

© 2023 S. Karger AG, Basel.

Auteurs

Renata Jaczyńska (R)

Department of Obstetrics and Gynaecology, Institute of Mother and Child, Warsaw, Poland.

Monika Bekiesinska-Figatowska (M)

Department of Diagnostic Imaging, Institute of Mother and Child, Warsaw, Poland.

Paulina Sobieraj (P)

Department of Diagnostic Imaging, Institute of Mother and Child, Warsaw, Poland.

Tadeusz Issat (T)

Department of Obstetrics and Gynaecology, Institute of Mother and Child, Warsaw, Poland.

Monika Gos (M)

Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.

Ewa Obersztyn (E)

Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.

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Classifications MeSH