Hyperreactio luteinalis associated with fetal hyperandrogenism and cystic hygroma.

Hyperreactio luteinalis cystic hygroma ovarian cysts pregnancy

Journal

Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 09 03 2022
revised: 05 06 2022
accepted: 25 08 2022
entrez: 14 9 2022
pubmed: 15 9 2022
medline: 15 9 2022
Statut: epublish

Résumé

A 23-year-old woman with a gestational age of 17 weeks presented with abdominal pain. The ultrasound showed maternal hyperreactio luteinalis with fetal cystic hygroma. After termination of pregnancy, the female fetus showed masculinization features with muscular hypertrophy. The hyperreactio luteinalis regressed under hormonal suppression therapy.

Identifiants

pubmed: 36101781
doi: 10.1002/ccr3.6310
pii: CCR36310
pmc: PMC9459097
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e6310

Informations de copyright

© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

The authors declare that there is no conflict of interest to be reported.

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Auteurs

Ali Ghassa (A)

Faculty of Medicine Damascus University Damascus Syria.

Dema Adwan (D)

Department of Obstetrics and Gynaecology Maternity University Hospital Damascus Syria.

Mhd Firas Safadi (MF)

Department of General Surgery, Visceral Surgery, and Proctology Diakonie Hospital Hartmannsdorf Germany.

Classifications MeSH