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Superficial acral fibromyxoma: insights from case management and comprehensive literature review.
Tan, Han Ling; Ahmad, Tunku Sara; Sankara Kumar, C; Khirusman Adnan, Yohan; Looi, Lai Meng; Gunasagaran, Jayaletchumi.
Afiliación
  • Tan HL; Department of Orthopaedic Surgery (NOCERAL), Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Ahmad TS; Department of Orthopaedic Surgery (NOCERAL), Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Sankara Kumar C; Department of Orthopaedic Surgery (NOCERAL), Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Khirusman Adnan Y; Department of Orthopaedic Surgery (NOCERAL), Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Looi LM; Department of Pathology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Gunasagaran J; Department of Orthopaedic Surgery (NOCERAL), Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
EFORT Open Rev ; 9(2): 129-137, 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38306799
ABSTRACT
Superficial acral fibromyxoma, also known as digital fibromyxoma, is a slow-growing, benign, solitary soft tissue tumor. First described in 2001 by Fetsch et al., it is a condition that often occurs in middle-aged individuals. However, it has also been reported across a wide range of ages, ranging from 4 to 86 years, with males more commonly reported. The condition often presents as solitary soft tissue swelling over the periungual or subungual. We present the management experience of the rare presentation of this rare tumor and a detailed review of the past literature on this condition. Detailed management of the condition has been described, along with the outcome after 2 years of follow-up and treatment experience. Our detailed analysis shows that 2 years is the shortest duration of follow-up to rule out recurrence. Hence, most of the cases reported earlier had given the false sense of the recurrence rate of the tumor, which could lead to undertreatment of the condition. The purpose of this article is to allow the readers to understand better the tumor's characteristics with bone involvement and the tumor's diagnostic strategies and treatment options.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: EFORT Open Rev Año: 2024 Tipo del documento: Article País de afiliación: Malasia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: EFORT Open Rev Año: 2024 Tipo del documento: Article País de afiliación: Malasia