Mao Allen, Rana Hunaid N, Elramah Mohamed, Martin Brett
Radiology, USA Health University Hospital, Mobile, USA.
Cureus. 2021 Jan 29;13(1):e12997. doi: 10.7759/cureus.12997.
The spectrum of presentation for patients who have neurofibromatosis type 1 (NF1), or von Recklinghausen disease, is very diverse due to a phenomenon known as variable expressivity. Patients may or may not present with cutaneous lesions or central nervous system (CNS) manifestations. However, multiple neurofibromas are the pathognomonic hallmark of NF1. The most common abdominal neoplasm is plexiform neurofibromas that affect the retroperitoneal region. We highlight the hospital course of a patient with an unknown history of NF1 who presented for head trauma with plexiform neurofibromas found incidentally on imaging. The radiographic features of neurofibromas are described in addition to the discussion of management and prognosis of NF1.
1型神经纤维瘤病(NF1),即冯雷克林霍增氏病患者的临床表现谱因一种称为可变表达的现象而非常多样。患者可能出现或不出现皮肤病变或中枢神经系统(CNS)表现。然而,多发性神经纤维瘤是NF1的特征性标志。最常见的腹部肿瘤是影响腹膜后区域的丛状神经纤维瘤。我们重点介绍了一名NF1病史不明的患者的住院过程,该患者因头部外伤就诊,影像学检查偶然发现丛状神经纤维瘤。除了讨论NF1的治疗和预后外,还描述了神经纤维瘤的影像学特征。