ArticleCureus2025
Scaphocapitate Fracture Syndrome in an Adolescent: A Case Report, Diagnosis, and Surgical Treatment.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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4 authors.
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Abstract
Scaphocapitate fracture syndrome, or Fenton syndrome, is a rare condition characterized by fractures of the scaphoid and capitate bones, often with a 180-degree rotation of the proximal capitate, and is frequently underdiagnosed due to its rarity and inconclusive initial radiographic findings. We report the case of a 15-year-old boy who sustained a high-energy wrist injury after a three-meter fall. Initial X-ray raised suspicion of a scaphocapitate fracture syndrome; therefore, the patient was referred for a CT scan. He returned with the results two months later, which confirmed scaphocapitate fracture syndrome. Surgical management involved open reduction and internal fixation of the scaphoid and capitate fractures, repair of the iatrogenic lunate fracture, and external fixation for stability. Postoperative recovery was satisfactory with complete fracture healing, no avascular necrosis, and minimal functional limitations at the five-year follow-up with a Modified Mayo Wrist Score of 100 out of 100 points. This case highlights the importance of high clinical suspicion, advanced imaging for accurate diagnosis, and anatomical surgical fixation to ensure alignment and favorable long-term outcomes.
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