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1.
Cureus ; 16(1): e52963, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38406127

ABSTRACT

Cubonavicular coalition is a rare congenital anomaly involving fibrous or osseous fusion between the cuboid and navicular bones. This case report presents a comprehensive analysis of a 10-year-old female patient with cubonavicular coalition, detailing the diagnostic challenges and tailored therapeutic interventions. The patient presented with persistent left foot pain and restricted range of motion. Clinical examination, radiographic studies, and magnetic resonance imaging confirmed cubonavicular coalition. Laboratory investigations ruled out systemic inflammatory processes. A multidisciplinary approach was adopted, initially employing nonsteroidal anti-inflammatory drugs and physical therapy. Surgical resection of the coalition was performed due to persistent symptoms, leading to successful outcomes. This case report contributes valuable insights into the clinical presentation, diagnosis, and management of cubonavicular coalition in pediatric patients. The successful outcome underscores the importance of a comprehensive and individualized approach, providing a basis for informed decision-making in similar cases. Continued research is essential to refine therapeutic algorithms and enhance understanding of rare musculoskeletal anomalies.

2.
Cureus ; 15(12): e50156, 2023 Dec.
Article in English | MEDLINE | ID: mdl-38186409

ABSTRACT

Infantile hemangiomas are common vascular tumors in infancy, typically affecting the skin. However, intraconal orbital hemangiomas are rare and present diagnostic challenges due to their impact on critical structures within the orbit. We present the case of a 1-year-old male with progressive orbital swelling and proptosis. Initial conservative management with propranolol was attempted, but due to the lack of response, surgical resection of the intraconal hemangioma was performed. Pediatric orbital hemangiomas, particularly intraconal variants, pose distinctive diagnostic challenges. While conservative approaches, such as propranolol, align with evolving strategies for infantile hemangiomas, surgical intervention may be necessary in cases with an inadequate response. This case underscores the importance of recognizing the need for timely surgical intervention in pediatric orbital hemangiomas, even after initial conservative measures. Successful surgical outcomes contribute to understanding pediatric orbital pathology and emphasize the ongoing evolution of management strategies in this challenging clinical scenario.

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