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Lumbar fetiform teratoma; a case report.
Fazel Rahman Faizi1, Najibullah Rasouly1
1Radiology department, French Medical Institute for Mothers and Children (FMIC), Kabul, Afghanistan.
Fetiform teratoma, a rare congenital tumor, was successfully surgically removed from a 6-month-old infant. This case highlights the importance of distinguishing it from fetus in fetu based on skeletal structure.
Area of Science:
- Pediatric Surgery
- Developmental Biology
- Pathology
Background:
- Fetiform teratoma is a rare, highly differentiated mature teratoma with organoid structures.
- It is often mistaken for fetus in fetu, with the absence of an axial skeleton being a key differentiator.
Observation:
- A 6-month-old female infant presented with a lumbar mass.
- Imaging revealed a sac-like structure containing bowel segments, mesentery, and lymph nodes.
Findings:
- Surgical excision of the lumbar mass was performed.
- The mass was confirmed as a fetiform teratoma, a rare entity, particularly in this location.
Implications:
- This case expands the known clinical presentations of fetiform teratoma.
- Accurate differentiation from fetus in fetu is crucial for appropriate diagnosis and management.
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