Abstract

BackgroundFetus in fetu is a rare condition in which a malformed fetus is found in the body of a living twin. The retroperitoneum is the most common location of this condition. However, the sacrococcygeal region is a rare site of the disease. The presence of vertebral bodies and limbs differentiates FIF from teratoma. Imaging modalities are important for diagnosing FIF.Case presentationA 12-months old boy was hospitalized because of a mass in the sacrococcygeal region. CT showed a large, complex mass with bony structure resembling sacrococcygeal bone, hip bone and the femur in the sacrococcygeal region of the boy. The blood supply of the mass was from the aorta of the host. MRI revealed the mass was connected with the dilated sacral canal of the host, which resulted in tethered cord. A preoperative diagnosis of FIF was made and surgery was performed to remove the mass. Surgical removal and subsequent pathological examination revealed the anencephalic fetus had limb buds and a sacrum but no axial skeleton, which supported the diagnosis of FIF. Conclusions CT and MRI played important roles in diagnosing FIF based on the location of the lesion.

Highlights

  • BackgroundFetus in fetu is a rare condition that can occur from the cranial cavity to the scrotal sac with the sacrococcygeal region the least common site of origin [1,2,3]

  • Fetus in fetu is a rare condition in which a malformed fetus is found in the body of a living twin

  • A total of 80% of Fetus in fetu (FIF) cases are located in the retroperitoneal space, while other cases are located in rare sites including the oral cavity, the cerebral ventricles, mediastinum, pelvis and the scrotum

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Summary

Background

Fetus in fetu is a rare condition that can occur from the cranial cavity to the scrotal sac with the sacrococcygeal region the least common site of origin [1,2,3]. FIF is a congenital anomaly that is secondary to abnormal embryogenesis in a diamniotic, monochorionic and monozygotic twin [4]. Whether FIF is a separate disease or it is a form of highly differentiated teratoma is still controversial [5]. To the best of our knowledge, only 1 case of FIF in the sacrococcygeal region has been reported [6]. We. Case presentation A 12-months old boy was hospitalized because of a mass in the sacrococcygeal region. The sacrococcygeal mass was detected by prenatal US at 34 week’s gestational age. The patient had no other congenital anomalies.

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