Oral Malignant Melanoma in a Patient With Neurofibromatosis Type 1: An Extremely Rare Association

被引：0

作者：

Berhili, Soufiane ^{[1
,2
]}

Rezzoug, Mohammed ^{[2
,3
]}

Ben Sghier, Ahmed ^{[2
]}

Moukhlissi, Mohammed ^{[2
,4
]}

Mezour, Loubna ^{[2
,4
]}

机构：

[1] Mohammed First Univ, Fac Med & Pharm, Oujda, Morocco

[2] Mohammed VI Univ Hosp, Dept Radiat Oncol, Hassan II Oncol Ctr, Oujda, Morocco

[3] Mohammed Premier Univ, Fac Sci, LPMR, Oujda, Morocco

[4] Mohammed Premier Univ, Fac Med & Pharm, Oujda, Morocco

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2022年 / 14卷 / 05期

关键词：

rare association; von recklinghausen disease; radiotherapy; neurofibromatosis type 1; oral melanoma; MUCOSAL MELANOMA; ANORECTAL MELANOMA; RADIATION-THERAPY; LOCAL EXCISION; BENIGN-TUMORS; RADIOTHERAPY; HEAD; NECK; MANAGEMENT; PROGNOSIS;

D O I：

10.7759/cureus.25331

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Neurofibromatosis type 1 (NF1) is a genetic disorder associated with high rates of neural crest-derived tumors, both benign and malignant. Many series have identified cutaneous melanoma as a rare tumor among cancers occurring in individuals with NF1 disease, but the mucosal location has to date never been reported. In this paper, we report an oral melanoma occurring in a patient with NF1 disorder, diagnosed at a locally advanced stage, successfully managed by definitive external beam radiotherapy, along with a comprehensive literature review on the melanoma-NF1 association.

引用

页数：9

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