Schick B, Plinkert P K, Prescher A
Klinik für HNO-Krankheiten, Kopf- und Halschirurgie, Universitätskliniken des Saarlandes, Homburg/Saar.
Laryngorhinootologie. 2002 Apr;81(4):280-4. doi: 10.1055/s-2002-25322.
Even though numerous theories have speculated either on the vascular or fibrous tumour component as tissue of origin, aetiology of angiofibroma still remain unclear. Histological investigations recently led Beham and coworkers to the assumption that angiofibromas have to be considered as vascular malformations.
After giving a literature review of the various theories on tumour origin the proposal to consider angiofibromas as vascular malformations is discussed on an embryological base. Taking typical clinical features of the tumour and knowledge of vasculogenesis into account a new explanation for origin of the vascular tumour component is presented.
The vascular component of angiofibromas can be explained embryologically due to incomplete regression of the first branchial arch artery (vascular atavism). This vessel arises regularly between embryological day 22 and 24 and recedes during regular development completely until delivery via temporary formation of a vascular plexus. In the late stages of embryological development remnants of the plexus are found at the area of the sphenopalatine foramen, the typical site of angiofibroma origin. Incomplete regression of the vascular plexus of the former first branchial arch artery may form the vascular component of an angiofibroma arising due to growth stimulation at the time of adolescents.
Incomplete regression of the first branchial arch artery presenting an atavism is suited to explain the vascular tumour component of angiofibromas considering main tumour characteristics (origin in the posterior nasal cavity close to the sphenopalatine foramen, main blood supply from the maxillary artery with possible feeders arising from the internal carotid artery). Our embryological contributions support to define angiofibromas as vascular malformations.
尽管众多理论对血管或纤维瘤成分作为起源组织进行了推测,但血管纤维瘤的病因仍不清楚。最近的组织学研究使贝哈姆及其同事认为血管纤维瘤应被视为血管畸形。
在对关于肿瘤起源的各种理论进行文献综述后,从胚胎学基础讨论了将血管纤维瘤视为血管畸形的提议。考虑到肿瘤的典型临床特征和血管生成知识,提出了血管肿瘤成分起源的新解释。
血管纤维瘤的血管成分可从胚胎学角度解释为第一鳃弓动脉的不完全退化(血管返祖现象)。该血管通常在胚胎第22至24天出现,并在正常发育过程中通过临时形成血管丛而完全消退,直至分娩。在胚胎发育后期,在蝶腭孔区域可发现丛的残余,这是血管纤维瘤起源的典型部位。前第一鳃弓动脉血管丛的不完全退化可能在青少年时期因生长刺激而形成血管纤维瘤的血管成分。
呈现返祖现象的第一鳃弓动脉不完全退化适合解释血管纤维瘤的血管肿瘤成分,同时考虑到主要肿瘤特征(起源于后鼻腔靠近蝶腭孔,主要血供来自上颌动脉,可能有来自颈内动脉的分支供血)。我们的胚胎学研究有助于将血管纤维瘤定义为血管畸形。