Angiomatoid fibrous histiocytoma Ó? an adolescent with an unusual presentation and course

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.

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Publication Details

Journal
Portuguese Journal of Pediatrics
Published
2024-11-07
DOI
https://doi.org/10.24875/pjp.m24000458
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
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article

Angiomatoid fibrous histiocytoma Ó? an adolescent with an unusual presentation and course

Rafael Barroso Cabrera, Sara Isabel de Almeida, Cristina Kátya Torres Teixeira Mendes, Ana Lacerda et al.
Portuguese Journal of Pediatrics
Sarcoma Diagnosis and Treatment
article

Angiomatoid fibrous histiocytoma Ó? an adolescent with an unusual presentation and course

Rafael Barroso Cabrera, Sara Isabel de Almeida, Cristina Kátya Torres Teixeira Mendes, Ana Lacerda, S.C.O.M. de Sousa
article en

Abstract

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.

Portuguese Journal of PediatricsVol. 56(3)
Good health and well-being
Openalex Percentile: Top 62%
Sarcoma Diagnosis and Treatment
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