Fetus in Fetu: Lessons Learned from a Large Multicenter Cohort Study

Author:

Taher Heba M. A.1,Abdellatif Mostafa1ORCID,Wishahy Ahmed Mohamed Kadry1,Waheeb Saber2,Saadeldin Yasser2,Kaddah Sherif1,Abdulsattar Ayman Hussein1,Osman Mohamed Abdulkader3,El Tagy Gamal Hassan1,Elbarbary Mohamed M.14,Khairi Ahmad2,Tawfik Sherifa56,Anis Shady7,Anis Elia7,Farouk Moemn1,Abdelfattah Ahmed Hamdy1,Muensterer Oliver J.8

Affiliation:

1. Department of Pediatric Surgery, Kasr Alainy Faculty of Medicine, Cairo University, Giza, Egypt

2. Department of Pediatric Surgery, Alexandria University, Alexandria, Germany

3. Department of Pediatric Surgery, Assiut University, Assiut, Egypt

4. Department of Pediatric Surgery, Barbary Pediatric Surgery Clinic, Dokki, Giza, Egypt

5. Department of Pathology, University of Lusaka, Lusaka, Zambia

6. Department of Pathology, Egypt Ministry of Health and Population, Cairo, Egypt

7. Department of Pathology, Cairo University, Giza, Egypt

8. Department of Pediatric Surgery, University Medicine Mainz, Mainz, Rhineland-Palatinate, Germany

Abstract

Abstract Introduction Fetus in fetu (FIF) is an extremely rare condition of abnormal twinning during embryogenesis. Most publications are single case reports. We describe the combined experience of four large tertiary referral centers with FIF which were not previously reported or published, and thereby draw conclusions to establish criteria for the workup, diagnosis, and management including intraoperative risk. Materials and Methods A survey was forwarded to a national pediatric surgery group which includes members from all pediatric surgery centers in the country enquiring about unpublished cases of FIF encountered over a 20-year interval. The cohort was analyzed for age of presentation, type of presentation, diagnostic workup, surgical management, and outcome. Results From 1998 to 2018, a total of 10 FIF cases were included in the study. Mean age of presentation was 4 months. Computed tomography and ultrasound were the main preoperative diagnostic modality in our cohort. Resection of the mass was curative in nine cases. Two cases in which the FIF was in direct topographic proximity to the biliary tree suffered severe intraoperative or lethal postoperative complications. Conclusion Complete excision of FIF is the treatment of choice and generally results in excellent long-term quality of life. Mortality is rare and may be associated with biliary involvement and retroperitoneal right upper quadrant location of the FIF tends to be associated with increased risk in excision, and there is also a possible association with the presence of immature elements in the pathology report.

Funder

The participating departments

Publisher

Georg Thieme Verlag KG

Subject

Surgery,Pediatrics, Perinatology and Child Health

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