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Perineum Spindle Cell Sarcoma in Neurofibromatosis Type 1

Soft tissue neoplasm is common among patients with neurofibromatosis type 1 (NF-1). We present a case of a middle-aged woman with NF-1 who presented with a painless, insidiously increasing perineal mass for the past eight months. She underwent colonoscopy, computed tomography staging, magnetic reson...

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Detalles Bibliográficos
Autores principales: Sandrasecra, Sanjeev, Vasan, Senthil, Henry, Fitjerald, Abdullah, Salmi, Hashim, Mohd Nizam Md, Merican, Siti Rahmah Hashim Isa, Wong, Michael Pak-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OMJ 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941423/
https://www.ncbi.nlm.nih.gov/pubmed/36825248
http://dx.doi.org/10.5001/omj.2023.08
Descripción
Sumario:Soft tissue neoplasm is common among patients with neurofibromatosis type 1 (NF-1). We present a case of a middle-aged woman with NF-1 who presented with a painless, insidiously increasing perineal mass for the past eight months. She underwent colonoscopy, computed tomography staging, magnetic resonance imaging of the pelvis, core-needle biopsy, and later wide local excision of left perineum swelling. Histopathological examination showed a high-grade spindle cell sarcoma, which is a rare association among NF-1. Spindle cell sarcoma is a group of malignant soft tissue tumors with locally destructive growth with spindle-shaped neoplastic cells. The solitary spindle cell sarcoma of the perineum is rare, and wide local resection with a clear margin is the only treatment at present—the scarcely available evidence limiting the use of adjuvant chemotherapy, immunotherapy, and radiotherapy.