Cormier J M, Cormier F, Mayade F, Fichelle J M
Clinique de la Défense, Unité de Chirurgie et d'Explorations Vasculaires, Nanterre.
J Mal Vasc. 1999 Oct;24(4):281-6.
Type 1 neurofibromatosis (NF1) is the most frequently observed phacomatosis, but involvement of arterial trunks is uncommon. Expression depends on the localization and is not easily related to the causal condition. Seven patients with type 1 neurofibromatosis developed vascular manifestations (table I) disclosed by hypertension (n = 2) digestive angina (n = 1), arterial rupture (n = 1) and aneurysm of the subrenal aorta (n = 1). The diagnosis of NF1 was clear in 5 cases; in 2 cases, the diagnosis could only be established on the basis of pathology findings demonstrating dysplasia of the media with voluminous periadventitial hypertrophic nerves (table II). All the large arteries can be involved in NF1. A complete vascular work-up is needed to identify multiple arterial localizations as found in two of our cases. Thoraco-abdominal stenosis was observed in 5 cases leading, in 2 cases, to coarctation with a hemodynamic and functional impact requiring aortic revascularization. The most frequently observed localization involves the renal arteries: 3 of our patient had occlusive lesions of the renal arteries and in 2, aneurysms were observed. Three of our patients (including 2 of the preceding), had major occlusion of digestive arteries. Three other cases revealed an aneurysm of inflammatory subrenal aorta, a rupture of the iliac into the inferior vena cava and a rupture covered by a subclavian aneurysm. The indication for surgery depends on the arterial signs of associated complications (5 of our cases). In one case surgery was indicated to prevent rupture of a splenic artery aneurysm and an aneurysm of the subrenal abdominal aorta. Two cases were treated by exclusion (ilio-cava fistula) or excision (splenic aneurysm); renal or digestive revascularization was performed with arterial or venous autografts in young patients (3 cases). One extensive abdominal coarctation was repaired with a PTFE graft as were the subclavian and subrenal aorta aneurysms. One patient with an ilio-cava fistula died from collapsus. Long-term results of the revascularizations are satisfactory with good control of the hypertension and total regression of the digestive angina. Fibrodysplasia of the renal or digestive media occurring alone or thoraco-abdominal coarctation should suggest NF1 and lead to a complete work-up to identify other arterial localizations. Patients should be followed regularly to prevent complications which in case of rupture can be life-threatening.
1型神经纤维瘤病(NF1)是最常见的错构瘤病,但累及动脉干并不常见。其表现取决于病变部位,且与病因状况不易关联。7例1型神经纤维瘤病患者出现了血管表现(表I),表现为高血压(2例)、消化道绞痛(1例)、动脉破裂(1例)和肾下腹主动脉瘤(1例)。5例患者的NF1诊断明确;2例患者仅根据病理结果确诊,病理显示中膜发育异常伴大量外膜周围肥大神经(表II)。NF1可累及所有大动脉。需要进行全面的血管检查以确定如我们其中两例患者所发现的多处动脉病变。5例患者观察到胸腹段狭窄,其中2例导致缩窄,对血流动力学和功能产生影响,需要进行主动脉血管重建。最常累及的部位是肾动脉:我们的3例患者有肾动脉闭塞性病变,2例观察到动脉瘤。我们的3例患者(包括前述2例中的2例)有主要的消化道动脉闭塞。另外3例显示肾下腹主动脉炎性动脉瘤、髂动脉破裂进入下腔静脉以及被锁骨下动脉瘤覆盖的破裂。手术指征取决于相关并发症的动脉表现(我们的5例患者)。1例患者因脾动脉瘤和肾下腹主动脉瘤有破裂风险而进行手术。2例患者分别接受了封堵(髂腔静脉瘘)或切除(脾动脉瘤)治疗;年轻患者(3例)采用自体动脉或静脉进行肾或消化道血管重建。1例广泛的腹部缩窄以及锁骨下和肾下腹主动脉瘤采用聚四氟乙烯移植物修复。1例髂腔静脉瘘患者死于虚脱。血管重建的长期结果令人满意,高血压得到良好控制,消化道绞痛完全缓解。单独出现的肾或消化道中膜纤维发育异常或胸腹段缩窄应提示NF1,并需进行全面检查以确定其他动脉病变部位。应定期对患者进行随访,以预防可能危及生命的破裂并发症。