Imaging findings of type I neurofibromatosis with outcome of malignant peripheral nerve sheath tumor in the right lower extremity

Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder caused by mutations of the NF1 tumor suppressor gene, characterized by café‐au‐lait spots, neurofibromas, and Lisch nodules. Malignant peripheral nerve sheath tumor (MPNST) is an extremely rare malignancy with neural differentiation po...

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Veröffentlicht in:Journal of clinical ultrasound 2024-11, Vol.52 (9), p.1450-1452
Hauptverfasser: Liu, Wen‐hua, Yang, Lei, Wang, Xiao‐yi, Wang, Ting‐yi, Zheng, Guang‐mei, Zhu, Yu‐ting, Che, Shan
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container_end_page 1452
container_issue 9
container_start_page 1450
container_title Journal of clinical ultrasound
container_volume 52
creator Liu, Wen‐hua
Yang, Lei
Wang, Xiao‐yi
Wang, Ting‐yi
Zheng, Guang‐mei
Zhu, Yu‐ting
Che, Shan
description Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder caused by mutations of the NF1 tumor suppressor gene, characterized by café‐au‐lait spots, neurofibromas, and Lisch nodules. Malignant peripheral nerve sheath tumor (MPNST) is an extremely rare malignancy with neural differentiation potential. The lifetime risk of developing MPNST in NF‐1 patients is 8%–13%.
doi_str_mv 10.1002/jcu.23807
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subjects Adult
Diagnosis, Differential
Female
Hereditary diseases
Humans
Lower Extremity - diagnostic imaging
Magnetic Resonance Imaging - methods
Male
Malignancy
malignant peripheral nerve sheath tumor
myofibrillar ultrasound
Nerve Sheath Neoplasms - diagnostic imaging
Neurofibromatosis
Neurofibromatosis 1 - complications
Neurofibromatosis 1 - diagnostic imaging
neurofibromatosis type I
Neurofibromin 1
Nodules
Peripheral nerves
Recklinghausen's disease
Sheaths
Tumor suppressor genes
Tumors
title Imaging findings of type I neurofibromatosis with outcome of malignant peripheral nerve sheath tumor in the right lower extremity
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