Abstract
Although in counterpart, the sphenopalatine artery (SPA), has been well described in the medical literature, the sphenopalatine vein (SPV) has received scant attention. Therefore, the present anatomical study was performed. Additionally, we discuss the variations, embryology, and clinical significance of the SPV. Adult cadaveric specimens underwent dissection of the SPV. In addition, some specimens were submitted for histological analysis of this structure. The SPV was found to drain from the sphenoidal sinus and nasal septum. Small tributaries traveled through the nasal septum with the posterior septal branches of the SPA and nasopalatine nerve. The SPA and SPV were found to travel through the sphenopalatine foramen and another tributary was found to perforate the medial plate of the pterygoid process and to connect to the pterygoid venous plexus which traveled lateral to the medial plate of the pterygoid process. The vein traveled through the posterior part of the lateral wall of the nasal cavity with the posterior lateral nasal branches of the SPA and the lateral superior posterior nasal branches of the maxillary nerve. To our knowledge, this is the first anatomical study on the SPV in humans. Data on the SPV provides an improved anatomical understanding of the vascular network of the nasal cavity. Developing a more complete picture of the nasal cavity and its venous supply might help surgeons and clinicians better manage clinical entities such as posterior epistaxis, cavernous sinus infections, and perform endoscopic surgery with fewer complications.
In human anatomy, the sphenopalatine vein (SPV) has not been well characterized or studied in and it is typically, simply described as arising from the sphenopalatine foramen along with the sphenopalatine artery (SPA) and nasopalatine nerve. However, its location in the posterior nasal cavity implicates the vein in a variety of clinical pathologies which make knowledge of the anatomy critical for understanding various diagnoses and surgical procedures in this area, e.g., epistaxis and posterior nasal neurectomy, cavernous sinus infection, and nasal congestion in rhinitis. Although vascular network called “Woodruff’s plexus” has been well discussed, there is a lack of evidence of the vascular system in the area [1]. Therefore, the present anatomical study was performed to better elucidate this structure of the nasal cavity.
Eight embalmed cadaveric heads, derived from four males and four females, were used in this study. The mean age at the time of death was 85 years (range 78–94 years). Three were latex injected specimens and were used for gross anatomical dissection using the surgical microscope (Zeiss). Five specimens were used for histological observation.
Three cadaveric heads were bisected using a bone saw and separated into two parts, one with the nasal septum and the other without (Fig. 1). The SPV and its tributaries were dissected carefully and its relationship with the SPA, nasopalatine nerve, and sphenopalatine foramen was documented.
Five non-injected cadaveric heads were used for microscopic observation. The nasal septum and adjacent palate were harvested en bloc and an additional coronal section was made for histologic examination in three specimens (Fig. 2). In other two specimens, the lateral nasal wall with the nasal septum was harvested for histology.
All of five specimens were decalcified for 14 days using hydrochlonic acid and embedded in paraffin. Then, 5 µm slices were cut with a microtome. All five specimens were stained with Masson-trichrome.
No previous surgical scars were observed in the dissected area of any specimens. The present study was performed in accordance with the requirements of the Declaration of Helsinki (64th WMA General Assembly, Fortaleza, Brazil, October 2013). The authors state that every effort was made to follow all local and international ethical guidelines and laws that pertain to the use of human cadaveric donors in anatomical research [2].
The SPV and related venous plexus were observed at the inferior aspect of the sphenoidal sinus (Fig. 3). Following removal of the mucosa of the nasal septum, the SPV was found to drain from the sphenoidal sinus and nasal septum. Small tributaries traveled through the nasal septum with the posterior septal branches of the SPA and nasopalatine nerve. Here, we call these venous tributaries “posterior septal branches of the SPV.” The findings in the three specimens were consistent.
Following removal of the mucosa of the posterior part of the lateral wall of the nasal cavity, the SPA and SPV were found to travel through the sphenopalatine foramen and another tributary was found to perforate the medial plate of the pterygoid process and to connect to the pterygoid venous plexus which traveled lateral to the medial plate of the pterygoid process. This vein also drained from the sphenoidal sinus (Fig. 4). The vein traveled through the posterior part of the lateral wall of the nasal cavity with the posterior lateral nasal branches of the SPA and the lateral superior posterior nasal branches of the maxillary nerve. Here, we call these venous tributaries “posterior lateral nasal branches of the SPV.” The findings among the three specimens were consistent.
Multiple posterior septal branches of the SPA and SPV are seen in close proximity to one another (Fig. 5) and the findings among the three specimens were consistent.
Multiple posterior lateral nasal branches of the SPA and SPV are shown in close proximity (Fig. 6) and these findings in the two specimens were consistent.
The venous network in the nasal cavity is less described in the literature compared to the arterial vasculature. Descriptions on the venous drainage of the nasal cavity are limited to simple statements such as that they ‘accompany the arteries’ and form a rich submucosal network of plexuses in the posterior region of the septum and middle and inferior conchae. The nasal venous network can be divided further by large veins at their anterior and posterior extremities. Veins in the anterior nasal cavity communicate with the greater palatine veins, which eventually drain into the ophthalmic or facial veins. Veins in the posterior nasal cavity drain into the ethmoidal veins, which pass through the cribriform plate to the superior sagittal sinus, and also into the SPV, which join the venous plexuses of the palate and nasopharynx. The SPV receives drainage from vessels of the posterior nasal cavity and passes through the sphenopalatine foramen to join the pterygoid plexus in the infratemporal fossa [1, 3]. The SPV can penetrate the medial plate of the pterygoid process to join the pterygoid venous plexus (Fig. 4). It might also drain from the medial wall of the maxillary sinus [4].
The embryological origins of the SPV have not been described in the literature but examination of the development of the SPA and related nasal venous structures may provide insight into its embryology. It is understood that the aortic arch branches to the first pharyngeal arch form around the fourth to the fifth week of embryologic development. The SPA, including other branches of the maxillary artery are formed from the aortic sac via the aortic arch [5]. The SPV might develop in the similar period of time.
The nasal cavity is richly vascularized with a high pressure blood supply from both the internal and external carotid arteries [1]. Epistaxis represents one of the most common ear, nose and throat conditions encountered by emergency providers in the United States [6]. Posterior epistaxis occurs in approximately 10%–20% of cases and is attributable to bleeding that arises from branches of the sphenopalatine vessels. It is widely recognized that posterior nasal cavity bleeding is more profuse and harder to control than anterior bleeding [5-7]. An understanding of the SPV and its relationship to the nasal angioarchitecture may prove useful when performing endoscopic procedures such as ligation for control of posterior epistaxis and posterior nasal neurectomy.
The posterior lateral nasal branches and posterior septal branches of the SPV are the only venous pathways in the posterior nasal cavity as shown in the present study. As Lung speculated, both sympathetic and parasympathetic fibers are involved in causing nasal congestion in rhinitis [9]. Whether the autonomic stimulation increases or decreases the venous outflow, the SPV can be the pathway of drainage from the posterior nasal cavity, inferior aspect of the sphenoidal sinus, and medial wall of the maxillary sinus. In cats, stimulation of the cervical sympathetic trunk decreases both nasal airway resistance and sphenopalatine venous outflow [10, 11]. On the other hand, stimulation of the vidian nerve (pterygopalatine ganglion) [12] can increase both nasal airway resistance and sphenopalatine venous outflow [11, 13]. In dogs, it is known that blood from the nasal mucosa drains via two main pathways i.e., the anterior two thirds via the external (dorsal) nasal vein and posterior one third via the SPV [14]. Lung [9] speculated that both sympathetic and parasympathetic fibers are involved in causing nasal congestion in rhinitis.
In conclusion, to our knowledge, this is the first anatomical study on the SPV in humans. Data on the SPV provides an improved anatomical understanding of the vascular network of the nasal cavity. The localization of the SPV near important posterior nasal landmarks such as the SPA and sphenopalatine foramen should also warrant greater clinical considerations and more accurate anatomic descriptions of the veins in the nasal cavity. Developing a more complete picture of the nasal cavity and its venous supply might help surgeons and clinicians better manage clinical entities such as posterior epistaxis, cavernous sinus infections, and perform endoscopic surgery with fewer complications.
Acknowledgements
The authors sincerely thank those who donated their bodies to science so that anatomical research could be performed. Results from such research can potentially increase mankind’s overall knowledge that can then improve patient care. Therefore, these donors and their families deserve our highest gratitude [15].
Notes
References
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