Skip Navigation LinksHome > Current Issue > Sacrococcygeal teratoma: management and outcomes
Annals of Pediatric Surgery:
doi: 10.1097/01.XPS.0000450329.23885.6c
Original Articles

Sacrococcygeal teratoma: management and outcomes

Hassan, Hussam S.; Elbatarny, Akram M.

Collapse Box

Abstract

Background/aim

Sacrococcygeal teratomas are the most common tumor during the neonatal period. They are either benign (mature) or malignant (immature, composed of embryonic elements). This retrospective study aims at reviewing our experience in management and outcome of this pathology during the period from January 2008 to November 2013.

Patients and methods

Charts were designed to collect the following data: the age at presentation, sex, clinical presentation, associated anomalies, Altman’s classification, investigations, management modality, tumor histology with respect to type and resection margins, outcome of treatment, and bowel or urinary complications.

Results

A total of 20 patients were included in this study. There were six male patients and 14 female patients. Ten patients were Altman type I, seven were type II, one was type III, and two were type IV. Surgical intervention was carried out using a posterior sacral approach in 17 patients (all type I and II patients) or combined abdominal and posterior sacral approaches in the remaining three patients (types III and IV). Recurrence occurred in two patients; these were types III and IV. We had one mortality. Two patients reported involuntary bowel movements, two reported frequent soiling, and five reported constipation.

Conclusion

Awareness about this pathology among practitioners is essential and would have avoided complications in this series. Early diagnosis and complete excision with removal of the coccyx is associated with good prognosis. Recurrence is related to tumor spillage during excision. Long-term lower gastrointestinal problems (constipation, fecal soiling) correlate with Altman’s classification of the tumor.

© 2014 Annals of Pediatric Surgery

You currently do not have access to this article.

You may need to:

Note: If your society membership provides for full-access to this article, you may need to login on your society’s web site first.

Login