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  Contents > Previous page > Article detail print Order
o Issue N# 5 - 2009 o

OTONEUROLOGY

Neurofibromatosis Type1 revealed by malignant peripheral nerve sheath tumour


Authors : Charfeddine I, Mnejja M, Hammami B, Hasnaoui M, Hadj K. A, Frikha I, Makni S, Boudawara T, Chakroun A, Ghorbel A. (Sfax)

Ref. : Rev Laryngol Otol Rhinol. 2009;130,5:327-330.

Article published in french
Downloadable PDF document french



Summary : Neurofibromatosis type 1 or Von Recklinghausen’s disease is an affection with variable clinical expression. Malignant transformation is rare and dangerous. Objective: The aim of this work is to study diagnostic criterias as well as treatment of this malignant transformation. Case report: Sixteen years old patient presented with gradually progressive basicervical mass without compression nor dysthyroidy signs. Physical examination revealed a painless, hard and well limited mass measuring 4 cm. It was located in front of sternal manubrium and associated to multiples “café au lait” spots, iris Lisch nodules and generalized neurofibromas. This mass was excised by cervical surgery. The histological exam concluded to a low grade malignant peripheral nerve sheath tumour. Unfortunatly, despite a larger reoperation including resection of the manubrium, the limit of this excision were not safe. Early recurrence was observed, although treated by surgery, chemotherapy and radiotherapy, the patient died by mediastinal invasion.

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