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May 31, 2026Sultan Qaboos University medical journal0 citationsOpen Access

Successful Laparoscopic-Assisted Management of a Rare Purely Cystic Type IV Sacrococcygeal Teratoma in Neonate: A case report

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AAAlghalya Khalid AlmaawaliSultan Qaboos UniversityAAAhmed AlwahaibiOman Medical CollegeYAYousuf Al-ShaqsiSultan Qaboos University Hospital

Key Points

  • To present the successful laparoscopic-assisted management of a rare purely cystic type IV sacrococcygeal teratoma in a neonate.
  • Laparoscopic-assisted cyst excision and coccygectomy performed on a 2-week-old female neonate
  • Imaging used to identify the purely cystic presacral lesion
  • Histopathological analysis confirmed diagnosis of mature cystic SCT.
  • Postoperative course was uneventful with minor wound dehiscence that resolved conservatively
  • Follow-up indicated complete wound healing with no recurrence
  • Demonstrates feasibility and safety of laparoscopic techniques in neonates with rare SCT.

Abstract

Type IV sacrococcygeal teratomas (SCTs) are the rarest subtype of SCTs. We report a 2-week-old female who presented to a tertiary care centre in Muscat, Oman, in 2024 with abdominal distension and feeding intolerance. Imaging revealed a purely cystic presacral lesion, managed with successful laparoscopic-assisted cyst excision and coccygectomy. Histopathology confirmed a mature cystic SCT and the patient was diagnosed with a purely cystic Altman type IV SCT. The postoperative course was uneventful apart from minor wound dehiscence, which resolved with conservative management. Follow-up showed complete wound healing and no recurrence. Purely cystic Type IV SCTs are extremely rare and challenging to diagnose due to their benign radiological appearance and lack of external manifestations. Complete surgical excision with coccygectomy remains the cornerstone of treatment; laparoscopic-assisted excision in neonates is feasible and safe.

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Cite This Study

Almaawali et al. (2026) studied this question.

synapsesocial.com/papers/6a1bd2ab5783ba022b6fe0fdhttps://doi.org/10.18295/2075-0528.2993
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