Abstract. Background The murine species are often used as an in vivo model due to their relatively short developmental period and comparatively cheap price. To evaluate the pathologic mechanism or effect of a new treatment or medication, a large sized mammalian is the optimal. However, there are major limitations for their use in experimental studies. As a result, a murine animal is often chosen instead. But, in these smaller animals, there are challenges, including the relatively small size of the head and neck structures, challenges in identifying the vascular and neural anatomy and the unavailability of a surgical atlas of normal anatomy.Previous studies suffered from two major problems. First, dissection produced trauma to the microvascular system, resulting in staining of the entire dissection field. This problem was aggravated whenever major vessels had to be removed. Second, attempts to avoid this problem, by first using formaldehyde to fix the tissues, made delicate 861