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Lipofibromatosis arising in a right labiocrural fold in a 14-month-old female: a case report study with a 3-year follow-up.
Zvizdic, Zlatan; Milisic, Emir; Bilalovic, Nurija; Ibisevic, Nermina; Bukvic, Melika; Vranic, Semir.
Afiliación
  • Zvizdic Z; Department of Pediatric Surgery, Clinical Center University of Sarajevo, Sarajevo 71000, Bosnia and Herzegovina.
  • Milisic E; Department of Pediatric Surgery, Clinical Center University of Sarajevo, Sarajevo 71000, Bosnia and Herzegovina.
  • Bilalovic N; Department of Pathology, Clinical Center University of Sarajevo, Sarajevo 71000, Bosnia and Herzegovina.
  • Ibisevic N; Department of Pathology, Clinical Center University of Sarajevo, Sarajevo 71000, Bosnia and Herzegovina.
  • Bukvic M; Department of Radiology, Clinical Center University of Sarajevo, Sarajevo 71000, Bosnia and Herzegovina.
  • Vranic S; College of Medicine, Q.U. Health, Qatar University, Doha 2713, Qatar.
J Surg Case Rep ; 2024(1): rjad728, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38213409
ABSTRACT
Lipofibromatosis (LF) is a rare benign fibrofatty tumor of infancy and childhood with a predilection for distal extremities, poor margination, and a high local recurrence rate. We report a toddler who presented with an LF involving her right labiocrural fold. Imaging showed a soft tissue mass extending through the right labiocrural fold with possible infiltration into the underlying muscles. The mass was excised entirely, preserving adjacent structures. The histopathologic report revealed the mass to be LF. A 3-year follow-up revealed no disease recurrence. No other cases of LF in this localization have been presented in the literature. Despite its rarity, LF should be considered in diagnosing soft tissue neoplasms in children. Accurate diagnosis and proper surgical management with complete resection are essential to reduce the postoperative recurrence risk.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Surg Case Rep Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Surg Case Rep Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido