Zihni Sanus Galip, Tanriverdi Taner, Akar Ziya
Department of Neurosurgery, Istanbul University, Cerrahpasa Medical Faculty, Cerrahpasa, 34301, Istanbul, Turkey.
Surg Neurol. 2007 Jun;67(6):634-8; discussion 639. doi: 10.1016/j.surneu.2006.09.034.
Orbital hypertelorism is defined as a lateralization of the total orbit. This condition is associated almost always with congenital abnormalities. An acquired total displacement of the orbit is almost impossible once the bony pillars of the craniofacial complex are established. The aim of this article was to discuss a case of a young man with paranasal sinus mucocele, who developed OHT.
A 20-year-old man was admitted to us with orbital hypertelorism in 1993. The patient's examination revealed marked orbital hypertelorism, and no other abnormal finding was noted, and he had no congenital defect at birth. Hypertelorism was corrected by surgery, and we find that this condition was acquired secondary to paranasal sinus mucocele.
This is the second case of an acquired OHT secondary to paranasal sinus mucocele and the first in which the condition was corrected by surgery in late years of life. We found excellent correction of orbital hypertelorism 13 years after surgery. The authors discuss the possible link between mucocele and possible mechanism for the development of orbital hypertelorism and emphasize the need for early surgery and long-term follow-up.
眶距增宽症定义为整个眼眶的侧向移位。这种情况几乎总是与先天性异常相关。一旦颅面复合体的骨支柱形成,眼眶的后天性完全移位几乎是不可能的。本文旨在讨论一例患有鼻窦黏液囊肿并发展为眶距增宽症的年轻男性病例。
一名20岁男性于1993年因眶距增宽症入院。患者检查显示明显的眶距增宽,未发现其他异常,且出生时无先天性缺陷。通过手术矫正了眶距增宽,我们发现这种情况是继发于鼻窦黏液囊肿。
这是第二例继发于鼻窦黏液囊肿的后天性眶距增宽症病例,也是第一例在晚年通过手术矫正该病症的病例。我们发现在手术后13年眶距增宽得到了极佳的矫正。作者讨论了黏液囊肿与眶距增宽症发展的可能机制之间的潜在联系,并强调了早期手术和长期随访的必要性。