Evidence map›Paper›PMID 41000244›Full record

ArticleSurgical case reports2025

Concurrent Prolapsed Omphalocele and Giant Hepatic Cyst Initially Suspected as an Umbilical Cord Cyst in the Prenatal Period: A Case Report.

Yuta Takeuchi, Seiichiro Inoue, Yuki Muta, Keisuke Sawada, Taisuke Hayashi, Kohei Kawaguchi, Akio Odaka

Abstract readCase Reports
In one paragraph

Article in Surgical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yuta TakeuchiDepartment of Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Seiichiro InoueDepartment of Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Yuki MutaDepartment of Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Keisuke SawadaDepartment of Pathology, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Taisuke HayashiDepartment of Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Kohei KawaguchiDepartment of Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Akio OdakaDepartment of Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionUmbilical cord cysts detected after the 2nd trimester of pregnancy are associated with a variety of complications, including omphalocele, and thus require careful monitoring. Congenital hepatic cysts are rare, as are reports of their coexistence with omphaloceles. Herein, we present an unusual case of an omphalocele complicated by a large hepatic cyst that was initially suspected to be an umbilical cord cyst during the fetal period. CASE PRESENTATION: A male infant was delivered via caesarean section at 36 weeks of age, with ruptured membranes and cloudy amniotic fluid. Fetal ultrasonography at 16 weeks had previously revealed an omphalocele with intestinal prolapse, and at 20 weeks, an umbilical cord cyst was suspected. At birth, the herniation sac ruptured, and abdominal wall closure and cyst excision were performed. The cyst, initially thought to be umbilical in origin, was instead identified as a hepatic cyst connected to the liver. Pathological examination confirmed the diagnosis. The infant was further diagnosed with Beckwith-Wiedemann syndrome, and was ultimately discharged 32 days postoperatively, with no recurrence to date.

conclusionsAlthough asymptomatic congenital liver cysts can often be managed conservatively with follow-up, we considered surgical intervention necessary in this case due to the presence of an omphalocele associated with suspected Beckwith-Wiedemann syndrome.

Indexed as

Beckwith–Wiedemann syndromehepatic cystomphaloceleumbilical cord cyst

Identifiers

PMID41000244
PMCPMC12457713

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