A Rare Case of Neuroendocrine Tumor in a Patient With Neurofibromatosis Type 1: Is There Any Association

被引：0

作者：

Baddi, Fatima Zahra ^{[1
,2
]}

Ahsayen, Fatima Zohra ^{[3
,4
]}

Ramdani, Hiba ^{[5
,6
]}

Rhazari, Meriem ^{[1
,2
]}

Skiker, Imane ^{[3
]}

Thouil, Afaf ^{[1
,2
]}

Kouismi, Hatim ^{[1
,2
]}

机构：

[1] Mohammed VI Univ Hosp, Dept Resp Dis, Oujda, Morocco

[2] Mohammed I Univ, Fac Med & Pharm, Dept Pulmonol, Oujda, Morocco

[3] Mohammed VI Univ Hosp, Dept Radiol, Oujda, Morocco

[4] Mohammed I Univ, Fac Med & Pharm, Dept Radiol, Oujda, Morocco

[5] Mohammed VI Univ Hosp, Dept Med, Oujda, Morocco

[6] Mohammed I Univ, Fac Med & Pharm, Dept Med, Oujda, Morocco

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2022年 / 14卷 / 09期

关键词：

neurofibromatosis type 1 (nf1); risk factor; lung cancer; malignancies; neuroendocrine tumor; SOCIETY EXPERT CONSENSUS; CARCINOID-TUMORS; LUNG; DIAGNOSIS; MANAGEMENT; CANCER;

D O I：

10.7759/cureus.29621

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Neurofibromatosis type 1 (NF1) is an autosomal dominant condition characterized by cafe-au-lait spots, cutaneous neurofibromas, axillary and inguinal freckling, and iris Lisch nodules; however, the presentations vary greatly, even within families. NF1 is also a recognized risk factor for the development of malignancy particularly malignant peripheral nerve sheath tumors (MPNST), optic gliomas, other gliomas, and leukemia. Nevertheless, the occurrence of lung cancer in a patient with neurofibromatosis type 1 is a rare phenomenon.

引用

页数：6

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