Home » 2025 » Volume 56 - Number 3 » Angiomatoid fibrous histiocytoma – an adolescent with an unusual presentation and course
Sara Isabel de Almeida 1, Sofia Cochito Sousa 2, Cristina Mendes 3, Rafael Cabrera 3, Ana Lacerda 3
1 Paediatric Department, Hospital Beatriz Ângelo, Loures, Portugal; 2 Paediatric Department, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal; 3 Department of Paediatric Oncology, Portuguese Institute of Oncology, Lisbon, Portugal
Sara Isabel de Almeida, Sofia Cochito Sousa, Cristina Mendes, Rafael Cabrera, Ana Lacerda
La información completa de afiliaciones y autor de correspondencia está disponible en la versión original en PDF.
*Correspondence: Ana Lacerda, Email not available
Introduction: Angiomatoid fibrous histiocytoma is a rare soft tissue neoplasm, which usually presents as an indolent mass in children and young adults and is often mistaken for a hematoma or hemangioma. Suspecting this diagnosis from imaging findings may be challenging, leading to diagnostic delays. Prognosis is generally favorable and metastases are infrequent at presentation. Case report: We describe the case of an adolescent who presented with a two-month history of a growing mass in the left scapular region, where diagnosis was made possible through surgical biopsy. Discussion: There were loco-regional lymphatic invasions and lung metastases at admission, and despite surgery and chemotherapy the disease rapidly progressed to death.