Abstract
Objective: Tumors of congenital origin differ in their symptoms and signs, predominant location and prognosis from those occurred later in childhood. To determine whether the prognosis of congenital (infantile) fibrosarcoma in the retroperitoneum, an extremely rare form of soft tissue malignant tumor, can be assessed prenatally. Methods: We describe a case of this condition diagnosed in utero, including the assessment of the tumor behavior by ultrasound and magnetic resonance imaging. We also review the English language literature in Medline over the past 10 years and describe the management options available in such cases. Results: Our case had precise prenatal findings revealed unfavorable conditions such as bulky tumor mass, spinal metastasis and pulmonary hypoplasia. Conclusion: Fetal imaging studies could accurately identify the invasion of tumor. The outcome is usually poor, especially for those fetuses affected by an axial location of the tumor.
| Original language | English |
|---|---|
| Pages (from-to) | 266-271 |
| Number of pages | 6 |
| Journal | Fetal Diagnosis and Therapy |
| Volume | 20 |
| Issue number | 4 |
| DOIs | |
| State | Published - 07 2005 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Congenital fibrosarcoma
- Magnetic resonance imaging
- Prenatal diagnosis
- Ultrasound
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