Imaging and outcomes of fetal adrenal hemorrhage: A systematic review

Author:

Pham Amelie1ORCID,Biswas Sonia2,Levy Ariel3ORCID,Spiliopoulos Michail4ORCID,McLaren Rodney5,Makhamreh Mona M.6,Al‐Kouatly Huda B.5ORCID

Affiliation:

1. Division of Maternal Fetal Medicine Department of Obstetrics and Gynecology Vanderbilt University Medical Center Nashville Tennessee USA

2. Department of Obstetrics and Gynecology Monmouth Medical Center Long Branch New Jersy USA

3. Division of Maternal Fetal Medicine Department of Obstetrics and Gynecology Weill Cornell Medicine at New York Presbyterian Hospital New York New York USA

4. Division of Maternal Fetal Medicine Department of Obstetrics and Gynecology University of Miami Miami Florida USA

5. Division of Maternal Fetal Medicine Department of Obstetrics and Gynecology Jefferson University Philadelphia Pennsylvania USA

6. Department of Obstetrics and Gynecology Maimonides Medical Center Brooklyn New York USA

Abstract

AbstractObjectiveTo describe prenatal and postnatal imaging findings of fetal adrenal hemorrhage (FAH) and its associated perinatal outcomes, including frequency of postnatal surgical intervention.MethodA systematic literature review of seven electronic databases was conducted from inception until January 2022, with 2008 articles identified reporting prenatally identified fetal adrenal masses. Studies with confirmed FAH diagnosis were included. Quality and risk assessment were evaluated.ResultsThirty‐five studies, including 102 FAH cases, were analyzed. FAH was commonly described as cystic (28/90, 31%), anechoic (25/90, 28%), or mixed echogenic (14/90, 16%) on ultrasound. Outcome data were available for 65 cases (64%) of FAH: 9% (6/65) resolved prenatally, 35% (23/65) resolved postnatally, 34% (22/65) regressed in size after birth, and 22% (14/65) persisted postnatally. Overall, 25% (16/65) of cases underwent postnatal surgical intervention. Neuroblastoma was suspected in all 16 surgical cases. Only one case (1/16, 6%) confirmed a cystic hematoma with microscopic islets of neuroblastoma in situ on pathology.ConclusionPrenatal diagnosis of FAH is challenging due to the significant heterogeneity of ultrasound findings. Final pathology did not support the need for surgical intervention. Persistent postnatal FAH warrants shared decision making for further management based on the clinical presentation.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

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