Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2022 Dec 28;16(1):482.
doi: 10.1186/s13256-022-03720-0.

Prenatal diagnosis of fetal midgut volvulus: a case report

Affiliations
Case Reports

Prenatal diagnosis of fetal midgut volvulus: a case report

Neelam Jain et al. J Med Case Rep. .

Abstract

Background: Fetal midgut volvulus is an uncommon yet potentially life-threatening condition. Prenatal diagnosis may pose a challenge, due to the paucity of specific signs and symptoms. Timely prenatal diagnosis of this condition is imperative to prevent fetal mortality and morbidity.

Case presentation: We present a rare case report of fetal midgut volvulus, malrotation, and intestinal obstruction at 32 weeks of gestation in a 31-year-old multigravida Indian patient who presented with decreased fetal movements. Fetal ultrasound revealed midgut volvulus with proximal bowel obstruction and polyhydramnios. The patient underwent emergency surgery, which revealed intestinal malrotation and confirmed the diagnosis of midgut volvulus. Untwisting of the volvulus was done followed by Ladd's procedure. Follow-up postoperative ultrasound was unremarkable.

Conclusions: Delay in the diagnosis of fetal midgut volvulus leads to poor fetal and maternal outcomes. Hence, it is vital for radiologists, sonologists, and obstetricians to be aware of this condition while performing fetal sonography. Prompt diagnosis and surgical intervention are vital to reduce the morbidity and mortality associated with this condition.

Keywords: Fetal midgut volvulus; Intrauterine; Malrotation; Ultrasound; Whirlpool sign.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
A,B Transverse transabdominal fetal sonography images demonstrating dilated bowel loops (white arrow) up to 2.3 mm (A) and classic “whirlpool sign” of twisted mesentery (yellow arrow) within the fetal abdomen (B)
Fig. 2
Fig. 2
Intraoperative view of the intestine demonstrating midgut volvulus

References

    1. Mustansir F, Farooq A, Baqir H, et al. A rare case of primary midgut volvulus necessitating extensive bowel resection in an adult. Cureus. 2019;11(6):e4833. doi: 10.7759/cureus.4833. - DOI - PMC - PubMed
    1. Park JS, Cha SJ, Kim BG, Kim YS, Choi YS, Chang IT, Kim GJ, Lee WS, Kim GH. Intrauterine midgut volvulus without malrotation: diagnosis from the ‘coffee bean sign’. World J Gastroenterol. 2008;14(9):1456–1458. doi: 10.3748/wjg.14.1456. - DOI - PMC - PubMed
    1. Gerçel G, Anadolulu Aİ. Intrauterine midgut volvulus as a rare cause of intestinal obstruction: a case report. J Med Case Rep. 2021;15:239. doi: 10.1186/s13256-021-02778-6. - DOI - PMC - PubMed
    1. Steffensen TS, Gilbert-Barness E, DeStefano KA, Kontopoulos EV. Midgut volvulus causing fetal demise in utero. Fetal Pediatr Pathol. 2008;27(4–5):223–231. doi: 10.1080/15513810802319608. - DOI - PubMed
    1. Best EJ, O’Brien CM, Carseldine W, Deshpande A, Glover R, Park F. Fetal midgut volvulus with meconium peritonitis detected on prenatal ultrasound. Case Rep Obstet Gynecol. 2018;2018:1–6. doi: 10.1155/2018/5312179. - DOI - PMC - PubMed

Publication types