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34 Vomeronasal Organ
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zees, with a comparison to other primates. Anat Rec. 2002;267(2):166–76.
19. Rodriguez I, Mombaerts P.Novel human vomerona­sal receptor-like genes reveal species-specic fami­lies. Curr Biol. 2002;12(12):R409–11.
20. Liman ER, Innan H. Relaxed selective pressure on an essential component of pheromone transduction in primate evolution. Proc Natl Acad Sci U S A. 2003;100(6):3328–32.
21. Rodriguez I, Greer CA, Mok MY, Mombaerts P. A putative pheromone receptor gene expressed in human olfactory mucosa. Nat Genet. 2000;26(1):18–9.
22. Liberles SD, Buck LB.A second class of chemosen­sory receptors in the olfactory epithelium. Nature. 2006;442(7103):645–50.
23. Pearson H.Mouse data hint at human pheromones. Nature. 2006;442(7102):495.
24. Rodewald A, Mills D, Gebhart VM, Jirikowski GF. Steroidal pheromones and their potential tar­get sites in the vomeronasal organ. Steroids. 2019;142:14–20.
25. Vasuki AK, Fenn TK, Devi MN, Hebzibah TD, Jamuna M, Sundaram KK.Fate and development of human Vomeronasal organ- a microscopic fetal study. J Clin Diagn Res. 2016;10(3):AC08–11.
26. Monti-Bloch L, Grosser BI.Effect of putative phero­mones on the electrical activity of the human vom­eronasal organ and olfactory epithelium. J Steroid Biochem Mol Biol. 1991;39(4B):573–82.
27. Comfort A. Likelihood of human pheromones. Nature. 1971;230(5294):432–3 passim.
28. Russell MJ.Human olfactory communication. Nature. 1976;260(5551):520–2.
29. Meisami E, Bhatnagar KP.Structure and diversity in mammalian accessory olfactory bulb. Microsc Res Tech. 1998;43(6):476–99.
30. Gower DB, Ruparelia BA. Olfaction in humans with special reference to odorous 16-androstenes:
their occurrence, perception and possible social, psychological and sexual impact. J Endocrinol. 1993;137(2):167–87.
31. Doty RL. Olfaction. Annu Rev Psychol. 2001;52:423–52.
32. Berliner DL, Monti-Bloch L, Jennings-White C, Diaz-Sanchez V.The functionality of the human vom­eronasal organ (VNO): evidence for steroid receptors. J Steroid Biochem Mol Biol. 1996;58(3):259–65.
33. Biehl MJ, Raetzman LT. Developmental origins of hypothalamic cells controlling reproduction. Semin Reprod Med. 2017;35(2):121–12.
34. Salazar I, Barrios AW, SáNchez-Quinteiro P. Revisiting the Vomeronasal system from an integrated perspective. Anat Rec (Hoboken). 2016;299(11):1488–91.
35. Baum MJ, Bakker J.Roles of sex and gonadal steroids in mammalian pheromonal communication. Front Neuroendocrinol. 2013;34(4):268–84.
36. Morozova SV, Savvateeva DM, Svistushkin VM, Toporkova LA.The role of the vomeronasal system in the formation of the human sexual behaviour. Vestn Otorinolaringol. 2017;82(2):90–4.
37. Monti-Bloch L, Diaz-Sanchez V, Jennings-White C, Berliner DL. Modulation of serum testosterone and autonomic function through stimulation of the male human vomeronasal organ (VNO) with pregna­4,20-diene-3,6-dione. J Steroid Biochem Mol Biol. 1998a;65(1–6):237–42.
38. Frasnelli J, Lundström JN, Boyle JA, Katsarkas A, Jones-Gotman M. The vomeronasal organ is not involved in the perception of endogenous odors. Hum Brain Mapp. 2011;32(3):450–60. https://doi.
org/10.1002/hbm.21035.
39. Grammer K, Fink B, Neave N.Human pheromones and sexual attraction. Eur J Obstet Gynecol Reprod Biol. 2005;118(2):135–42.
Physiology oftheNasal Cartilages
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andTheir Importance toRhinosurgery
WolfgangPirsig
35
Core Messages
• The complex framework of the human nasal cartilages, unique among mammals, is the mobile portal to the respiratory system provid­ing conditions for the passage of airstreams and the generation of nasal resistance and turbulence.
• The septodorsal (septolateral) cartilage is the dominating structure for nasal and midfacial growth and is decisive for the appearance and several functions of the nose. Together with the erectile lining of the nasal cavities, the car­tilaginous framework enables air-conditioning and the acting of the nasal cycle.
• The anterior nose with the nasal valve as its crucial functional region is the narrowest part of the upper airways and provides two-thirds of the total airaway resistance.
• Due to its protruding exposition, it is espe­cially vulnerable to external injuries and may react as a protecting crumpled zone. This exposition also is the reason why most of the obstructing structures of the nasal airways are diagnosed in the anterior nose.
• Long-term observations have shown that the most effective outcome after functional and aesthetic rhinosurgery is achieved by focusing on restoring the physiological functions of the
W. Pirsig (*) Department of Otorhinolaryngology, University Hospital Ulm, Ulm, Germany e-mail: wolfgang.pirsig@uni-ulm.de
anterior nose, the site of the most resistive nasal segments.
The human nose, with its prominent bridge, its elongated tip, and its downturned nostrils, is unique. Besides snifng strange odours, it acts as a vital air-conditioning unit, warming, cleaning, and moistening the air we breathe in before it reaches the delicate lungs. Assisting this—and also adding resonance to the voice—are the nasal sinuses, but the price we pay for possessing these valuable cavities is an all too common suscepti­bility to local infections.
This precise summing up of the appearance and functions of the nose including its Achilles’ heel tendon, the diseases, was published in 1985 by the zoologist Desmond Morris in his outstand­ing book Bodywatching [1].
In the following chapter, I’ll focus on some functional aspects of the cartilaginous framework of the human nose with an emphasis on its vul­nerability and long-term results following surgi­cal treatment. Why do we have a nose of such a protruding shape, which is divided by the septum into two parallel halves? Why is this mobile organ built up by a complex framework of hya­line cartilages and covered by muscles? Why do we need this nose at all, although we can survive by breathing through the mouth? I asked anato­mists, physiologists, rhinosurgeons, biologists, and also engineers for stream technology. The answers varied, several ended with a question
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 Ö. Ö. Celebi, T. M. Önerci (eds.), Nasal Physiology and Pathophysiology of Nasal Disorders,
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mark, but in all of them the terms ‘turbulence’, ‘resistance’, and ‘air-conditioning’ were some­how mentioned.
35.1 Part I: Anatomical Considerations
35.1.1 Nomenclature
The lower two-thirds of the nose are built up by a framework of the following hyaline cartilages: septal cartilage (quadrangular cartilage in adult­hood), a partition separating the two nasal cavi­ties; soft tissue part of the septum is the septal turbinate (septal body or intumescentia septi or septal tuberculum); two triangular (upper lateral) cartilages as expansions of the septal cartilage forming together the T-bar-shaped framework also known as septodorsal or septolateral carti­lage; two paraseptal (vomeronasal) cartilages, lying along the inferior margin of the caudal sep­tal cartilage, attached to the vomer posteriorly and to the maxillary crest anteriorly; two alar (lower lateral or lobular) cartilages composed of a medial and lateral crus melted together at the
dome on the tip; and some sesamoid (accessory) cartilages in the soft tissue area between triangu­lar cartilage, lateral crus and piriform aperture, in the so-called hinge area.
In this chapter, the terms septum, septal, sep­todorsal, paraseptal, triangular, alar and sesamoid cartilages will be used.
35.1.2 Intrauterine Development
A two-tube system and a still unrufed entrance are recognisable in the fourth month of foetal development of the cartilaginous nose (Fig.35.1). The cartilaginous framework consists of a T-bar­shaped bilateral vault fused in the midline to the septal cartilage. The complete sidewall of the car­tilaginous nasal capsule is superiorly connected with the spheno-ethmoidal cartilage and dorsally with the septal cartilage which posteriorly merges into the cartilaginous anterior skull base with the crista galli. Both vaults are separated by the supraseptal groove. Caudally, the margin of the sidewall bends medially to join with the inferior turbinate. Thus, the palatine bone, the vomer and the paraseptal cartilage are visible.
Apertura
externa
Cartilago
paranasalis
Cartilago
paraseptalis
Os maxillare
Fig. 35.1 Nasal skeleton of a foetus (8cm) in oblique side view [2]
Cartilago spheno-ethmoidalis
Foramen opticum
Os lacrimale
Os palatinum
Os vomeris
35 Physiology oftheNasal Cartilages andTheir Importance toRhinosurgery
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cartilages. The same happens to small processes of the lateral sidewall which are concealed by the semicircular cartilage in Fig.35.2. The paraseptal cartilages are concealed by the caudal part of the semicircular cartilages. The triangular cartilages are not yet differentiated. In the newborn, they are still continuous with the cartilaginous ante­rior skull base. Their caudal margins are rmly connected to the alar cartilages and to the piri­form aperture. In the newborn, the alar cartilages are developed as separate structures as in the adult and overlap with their cranial margins and the caudal margins of the triangular cartilages.
35.1.3 Postnatal Development
The septal cartilage of the newborn is progres­sively transformed from posteriorly, cranially and caudally into a unit of posterior bone and remaining anterior quadrangular cartilaginous plate as clearly depicted by Virchow in 1857 [3]. This old knowledge has recently been supported
Fig. 35.2 Model of the cartilaginous nasal capsule of a foetus (27.5cm, 30–32weeks) [2]
In the sixth foetal month, ingrowth of connec­tive tissue divides the cartilaginous nasal capsule into the individual septal cartilage, lateral carti­lages and alar cartilages. Thus, the complex carti­laginous nasal portal is developed which later forms the cartilaginous framework of the mobile nose.
In the model of the foetal cartilaginous cap­sule aged 30–32weeks (Fig.35.2), we look at the two vaults of the lateral cartilages fused together with the septal cartilage in the supraseptal groove. The median portion bida septi remains as the rest of the fusion of the vaults. Two semicircular­shaped cartilaginous bars have been almost com­pletely separated from the caudal septal cartilage. They encompass the nasal vestibule medially, dorsally and laterally to form the denite alar car­tilages. In the medial upper angle of the alar car­tilage, an isolated piece of cartilage is visible on the right-hand side, while on the left-hand side, it is still a process in connection with the left side­wall. Later, these pieces become the sesamoid
by Kim etal. [4] who evaluated the anatomical correlations among components of the nasal sep­tum using computed tomography. They found again that the area of the cartilaginous septum decreases with age, while the area of the perpen­dicular plate increases with age at the expense of the area of the septal cartilage. However, the area of the total nasal septum remains constant.
In the rst decade of life, the triangular carti­lages show regression from the cephalic to the caudal end under the nasal bones until being transformed into the approximately triangular shape of the adult nose. Only a small cartilagi­nous remnant of the triangular cartilage remains overlapped by the caudal margin of the nasal bone. Caudally, the triangular cartilages are overlapped by the cranial margins of the alar cartilages.
Very rarely the regression process of the trian­gular cartilage is retarded or even impeded. This may happen in the case of a median nasal stula or of a nasal dermoid cyst which can cranially end at the crista galli. Nasal bidity is another congenital malformation with impeded regres­sion of the triangular cartilages.
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Potter etal. [5] studied 35 adults, white cadav­eric specimens and specially focused on the cau­dal attachment of the triangular cartilage to the septal cartilage, where usually a small cleft facili­tates mobility between the caudal edge of the tri­angular cartilage and the septum, the so-called weak triangle of Converse. The attachment ranged from no cartilaginous connection (68%) to complete fusion (32%), i.e. a coincident loca­tion of the anterior septal angle and the caudal edge of the triangular cartilage.
In the adult, the relationship between the tri­angular cartilage and the lateral crus of the alar cartilage shows four variations [6]. Most often Dion etal. found an overlap of the caudal margin of the triangular cartilage by the cranial margin of the lateral crus. Less frequently are the rela­tionships ‘end to end’, ‘scroll’ and ‘opposed scroll’.
Each cartilage of the cartilaginous vault is encased in its own brous capsule, whose bres decussate, form a brous band or aponeurosis and join the capsule of adjacent cartilage. This aponeurosis, acting as a exible membrane, allows freedom of movement between the neigh­bouring cartilages. According to Hinderer [7], the most distinctive bres are:
Besides their mimic function, some muscles act as dilators of the valve region or openers of the nostrils or provide stability for the lateral nasal wall [9]. Especially, the dilator naris accompa­nies each nasal inspiration, thus directly varying with ventilation, nasal resistance, hypoxia and hypercapnia. It stabilises the anterior nasal air­way and precedes diaphragmatic contractions and ceases to act with mouth or tracheostomal breathing [10].
The framework of nasal cartilages with their brous connections and covering muscle layer acts as a shield and portal to the erectile lining of the nasal cavities. Eugene Kern from Rochester, USA, termed the nasal mucosa ‘the organ of the nose’ to sum up all its many functional tasks which are described in other chapters of this book. While the nasal vestibule is covered with squamous epithelium continuing some millime­tres around the edge of the caudal margin of the triangular cartilages, the nasal mucosa with cili­ated cylindrical epithelium starts in the posterior valve region [11, 12]. Figure35.3 shows the his­tological section through the posterior valve
1. Those between the terminal ends of the trian­gular cartilage and septum that supply the mobility necessary for valve action between these two structures.
2. Those between the caudal end of the septum and the medial crura of the columella which form the membranous septum.
3. Those between the caudal margin of the trian­gular cartilages and the cranial border of the alar cartilages.
A permanent continuity between the encasing brous capsule of the triangular cartilage and the periosteum of the nasal bone was found by Bruintjes etal. [8], supporting the clinical obser­vation of the rm connection between the nasal bones and the triangular cartilages.
Additional mobility of the interacting nasal cartilages is provided by the thin layer of seven muscles covering the external nasal pyramid.
Fig. 35.3 Section through the posterior valve region of a newborn cadaver specimen. Note heads of the inferior tur­binates deviated anterior septal cartilage with septal body and asymmetric maxilla. Haematoxylin-eosin (gift of Lindsay Gray/Perth to author 1975)
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region of a newborn. The heads of the inferior turbinates catch our eyes as elevations from the mucosal lining of the lateral walls. The slightly deviated cartilaginous septum with its mucosal lining presents its thickening in the middle cov­ered by the thick pad of erectile mucosa, the sep­tal body or intumescentia septi. The different thickness of the vertically cut septal cartilage is clearly visible: the thick cranial part merges cau­dally with a thin segment to end in the broad deviated cartilaginous foot embedded in the pre­maxillary bone. This pattern of different carti­laginous thicknesses remains persistent throughout its lifetime as investigated by van Loosen etal. [13].
35.2 Part II: Functional Aspects
In this book, nasal functions like breathing, resis­tance, turbulence and nasal cycle are treated in special chapters in detail. Thus, I can conne to a few comments on functions where nasal carti­lages are essentially involved like in the nasal valve region or the vulnerable anterior septum.
The anterior septodorsal cartilage, the para­septal and the alar cartilages with the sesamoid cartilages form the framework of the nasal lob­ule and thus the portal to the upper airways. Soft tissue connections between the cartilages of varying thickness and several small muscles act­ing on their outside enable mobility and/or sta­bility of the lateral nasal walls. Thus, the entrance to the nose can be dilated and narrowed to mod­ify the inspiratory and expiratory airstreams. The entrance of the airow is comparable with two at, oval, hollowed structures, the nasal vesti­bules, which terminate in the aperture between the septum and the caudal end of the triangular cartilages, both parts of the nasal valve region. The vestibule is at an oblique angle to the cavum [11]. According to Cole’s studies [10, 14] the nasal valve region consists of four anatomical airow-resistive components: the aperture between the septum and triangular cartilage, the bony entrance to the nasal cavum which is occu­pied by erectile tissues of both lateral (head of inferior turbinate) and septal nasal walls (includ-
ing the septal body) that modulate the cross­sectional area of the airway and airow resistance. Two-thirds of the total nasal resis­tance during inspiration is provided by the nasal valve region. This has clearly been proved by Haight and Cole [15] using pressure-sensing cannulas. As two- thirds of the total airway resis­tance to breathing is created in the nose—one­third is provided by the open mouth [16]—the nasal valve region is the main resistor of the total airway. The narrow nasal valve region with the smallest cross- sectional area of the nasal cavum accelerates the inspired air, creating turbulence. Valve constrictions disrupt the laminar charac­teristics of the inspired air as it enters the body of the cavum and thereby enhance exchanges with the nasal mucosa of heat, water and noxious materials. In the widened nasal cavum, airow decreases its speed [14].
In clinical praxis, the physician has to face several patients complaining of breathing prob­lems which are caused by a disturbed anatomy of the nasal valve region, especially patients with a tension nose or a saddle nose. A patient with a tense nose presents with a prominent, curved, small dorsum due to a too large and too high sep­tum. Other characteristics are the increased pro­jection of the tip, slitlike nostrils with an elongated columella and elongated thin nasal alae. The feet of the medial crura are cranially shifted, thus broadening the base of the colu­mella. The nasolabial angle is enlarged and often the upper incisivi are showing. The valve angle is less than 10° which results in a bilateral alar col­lapse during inspiration.
In the cartilaginous saddle nose, the septum is too short mostly due to fractures or perforations. The caudal septodorsal cartilage is depressed which causes an enlargement of the valve angle to more than 20°. The nostrils with ballooning alae are elliptically distorted; the columella is shortened and often retracted. Although the nasal cavities look very wide, the main complaint of the patients is insufcient breathing due to too much turbulence of the airstreams.
The fact that the nasal septum divides the nose into two parallel halves is the condition for cyclic activities of the erectile nasal mucosa. Kayser in
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1895 [17] rst reported on the spontaneous, cyclical congestion and decongestion in the nasal cavities. The anatomic conditions for this mucosal behaviour are mainly provided by its capacitance vessels. The ‘working phase’ of one nasal cavity characterised by decongestion of the cavernous tissues alternates with the ‘resting phase’ characterised by congestion of the mucosa [14, 18, 19]. Changes in ow and resistance dur­ing the nasal cycle have been studied using rhino­manometry [18, 20]. By means of acoustic rhinometry, Fisher et al. [21] measured the changes in the cross-sectional areas in the nasal cavities due to congestion and decongestion.
Using the combination of endoscopic imag­ing, rhinomanometry and acoustic rhinometry, Lang etal. [19] observed a periodic change in turbulence behaviour in addition to the known cyclical changes in ow resistance and nasal width. In the resting phase, the mainly laminar ow was found. During the working phase, the onset of turbulence occurred already at low velocities. The increase of turbulence during the working phase was created by the increase in cross-sectional area in the anterior cavum due to decongestion of the mucosa of the head of the inferior turbinate and the septal body. A special insight into the behaviour of the nasal cycle is measurable using the new method of long-term rhinoowmetry which yields infor­mation about the nasal cycle over a 24-h period [22]. This method is also of practical value in Sleep Medicine to investigate sleep-disordered breathing.
The nasal cartilages are insofar involved in the process of the nasal cycle as they provide the ana­tomical trigger zones for the transition from lam­inar to turbulent airow, namely, the anterior nasal cavum between the nasal valve region and the head of the middle turbinate.
Bruintjes etal. [8] studied the kinematics of the lateral nasal wall which is made up of three parts: (a) the osseous-cartilaginous chain of the nasal bone, triangular cartilage and the lateral crus of the alar cartilage; (b) the hinge area with the sesamoid cartilages between the lateral piri­form aperture and the lateral margin of the lateral crus; and (c) the ala, the part between piriform
aperture and alar cartilage, not supported by car­tilage. While part (a) is relatively stable and part (b) much more compliant, they found part (c) to be the most compliant part of the lateral nasal wall. They also studied the muscles inuencing the lateral nasal wall and its compliance. With this knowledge of the mechanical properties of the lateral nasal wall, they were able to analyse pathological clinical conditions, which may occur at the level of the nasal valve and at the level of the vestibule or nostril. Thus, they could explain, for instance, the physiological altera­tions caused by facial nerve palsy where muscle denervation may lead to alar collapse [23].
Loss of alar stability with nasal obstruction during inspiration is often caused by inadequate surgical procedures for the nasal lobule. Mostly the continuity of the osseous-cartilaginous chain, ‘nasal bone-triangular cartilage-lateral crus of alar cartilage’, is destroyed [24]. Detailed knowl­edge of these anatomical connections could help to reduce such adverse surgical sequelae.
The alar collapse associated with the drooping tip of elderly people may result from nasal mus­cle atrophy, a change in cartilage resilience and stretching of the intercartilaginous brous tissue with loss of cartilage overlap in the intercartilagi­nous junction [25]. The surgical procedure of the so-called rhinolift could reduce the breathing problems of elderly people. Via intercartilagi­nous incisions in the limen nasi, the cephalic margins of the lateral alar crura are bilaterally partly resected. After elevating the dorsal skin of the nasal pyramid and excision of an oval piece of skin in the nasal root, both mobilised alar car­tilages can be lifted and xed, thus widening the angles of the nasal valves.
The elastic nasal cartilages are useful ele­ments for protective functions. The 9-year-old boy in Fig.35.12 is a good example to explain the function of the septal cartilages as a ‘crumpled zone’ in case of severe anteroposterior load. Between 1970 and 1972, I performed septorhino­plasty according to the techniques of Cottle, Goldman and Masing in 92 children with a mean age of 10.5 years [27]. The indication was obstructed nasal breathing due to established post-traumatic nasal deformities. Intraoperatively,
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fractures and defects were visible in the anterior septodorsal cartilage with involvement of the nasal valves and sometimes of alar cartilages in 44/92 noses. These noses were damaged by loads from frontal and/or below. About 23/92 noses showed fractures in the septodorsal cartilage like the previous group and in addition fractures of the nasal bones and perpendicular plate were caused by the mainly anteroposterior load. This means that 67/99 or 72% of the children suffered nasal obstruction due to damaged nasal cartilages in the anterior nose.
The build-up of the septal cartilage in regions of different thicknesses [13] throughout the whole life is one component to react more elasti­cally to front load. The second component of more compliance is the vaultlike construction of the septodorsal and alar cartilages with their joint-like brous interconnections [8]. Note the distortion of the caudal septodorsal cartilage of the boy in Fig.35.12 (3): a 90° angle of the cau­dal septum with fractures in the caudal edge and depressed edges of the triangular cartilages. Van Velzen et al. [28] published the prepared septal cartilage of a 4-year-old boy who died in a frontal accident. The fracture lines in the cartilaginous septum followed the thin regions of the cartilage as sites of minor resistance in reaction to the load.
In idealised and patient-specic models, Lee etal. [29] recently published the reactions of the human septal cartilage exposed to anteroposte­rior load. They found the maximum stress areas in the nasal septum in the vicinity of the bony­cartilaginous junction and the anterior nasal spine, which are consistent with clinical experi­ence. The ndings of their study also suggest that the septum does function as a ‘crumpled zone’, absorbing a signicant amount of stress before it is transmitted to the skull.
The extreme variant of a damaged crumpled zone nose is the classic boxer’s nose, the so­called rubber nose, mainly formed by the alar cartilages. The septodorsal cartilage is shrunken to a minimum; nasal bones and anterior nasal spine are pressed down to the level of the piri­form aperture or resorbed.
35.3 Part III: Alterations ofNasal Cartilages
The functions of the nasal cartilages can best be recognised in children and adults with a disturbed cartilaginous framework. The growing nose is inuenced by genetic and epigenetic inuences such as oxygen supply, nutrition, hormones, medication, infections and injuries including nasal surgery as a controlled trauma, to name a few. In this part, examples are presented describ­ing some long-term inuences on the nasal carti­lages citing literature and own case reports.
35.3.1 Lacking Septodorsal
Cartilage
Already in utero, the septodorsal cartilage, being composed of the septal and both triangular carti­lages, develops as the dominating structure for nasal and midfacial growth. This was shown in 1791 by Soemmerring [30] who published a new­born’s skull with a lacking septodorsal cartilage and the skull of a healthy newborn for compari­son (Fig. 35.4). In the deformed newborn, the nasal bones and the incisive parts of the maxilla are not developed. The size of the piriform aper­ture is reduced to one-third in width compared with the healthy newborn. The height and width of the maxilla are reduced, while the contours of the orbital cavities are distorted compared with the healthy newborn.
35.3.2 Lacking Alar Cartilages
The following case shows that congenitally lack­ing both alar cartilages did not impede the growth of the nose and midface apart from the complete lacking nasal lobule (Fig.35.5). The 15-year-old boy came from a family with no genetic nasal disorders and an uneventful pregnancy of his mother. There was a complete absence of both alar cartilages. The pseudo-columella was formed by skin covering the caudal septal cartilage. The
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Fig. 35.4 Skulls of newborns lacking septodorsal cartilage (left), with normal midface (right) [30]
W. Pirsig
Fig. 35.5 Fifteen-year-old boy with congenital lack of both alar cartilages [31]
caudal margins of the triangular cartilages were covered by thick skin on the right and thin skin on the left side. All the other nasal structures were inconspicuous. The boy’s breathing was normal [31].
35.3.3 Physiological Septal Deviation
The anatomical term ‘physiological septal devia­tion’ was introduced by Zuckerkandl [32] who dened this type of septal deformation as a bent septum within the asymmetrical human skull. He published several examples on beautiful litho­graphs (Fig. 35.6). Comparable histologic sec-
tions of his own cases were published by Gray [33] who kindly left me a few of them like in Fig.35.3. In more recent publications [34, 35] on this topic, the incidence of the physiological sep­tal deviation is reported between 30% and 75% for children and between 13% and 96% in adults, with strikingly less patients reporting to suffer from subjective symptoms [36]. From the physi­ological point of view, it is practical to character­ise the physiological septal deviation by normal endonasal resistance [34]. Many of these physio­logical septal deviations develop during foetal life in connection with asymmetrical maxillary growth. Often the non-pathological role of this deviation is not recognised and a septal operation is indicated, although it is useless or even wors-
35 Physiology oftheNasal Cartilages andTheir Importance toRhinosurgery
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injury is documented in Lindsay Gray’s Fig.35.3. In neonates, two types of nasal deviation are observed: a septal dislocation that can easily be replaced in the midline and a nasal deviation that cannot be replaced by manipulation. The rst type is considered as nasal trauma during deliv­ery. The second type had been published by sev­eral authors since the end of the nineteenth century [37] and more detailed by Cottle [38] who generally concluded: ‘For these, expectant waiting is recommended unless there is complete inability to breathe and eat. One sees remarkable
Fig. 35.6 Physiological septal deviation in an asymmet­rical skull; The thicker spongiosa (a) compared to the thinner one (b) narrows the right maxillary sinus [32]
improvement in the appearance and development of these noses without surgical intervention. During the rst decade, however, some will
require surgical aid’. To nd out the incidence of ens the nasal symptoms. A septal body may be mistaken as pathological septal deviation or the real cause of nasal obstruction such as a problem of the nasal valve or an inspiratory ala collapse is failed to be recognised.
Until now, the diagnosis of the ‘physiologi­cal septal deviation’ has mainly been made by nasal endoscopy and the subjective history of the patient to be free of nasal breathing prob­lems. In a prospective cohort study, Gogniashvili etal. [34] investigated 158 patients between 18 and 40years using rhinoresistometry, acoustic rhinometry, endoscopy and visual analogue scales for subjective complaints. They dened the normal one-sided nasal resistance as less or equal to 0.35 sPalcm3 at a ow velocity of 250 cm3/s. Applying this benchmark, the unselected group of non-rhinological patients was differentiated into 144 subjects with physi­ological nasal resistance and 44 with pathologi­cal septal deviation. This means an incidence of
72.2% physiological septal deviation in an unselected cohort which ts well with the data mentioned above.
these two types of nasal deviation, we investi­gated 3425 children, born in 2 years between 1980 and 1981, in the Obstetric Department of the University of Ulm, Germany. A total of 110 (3.23%) of these neonates, belonging to the Caucasian population, showed deviated nasal structures. 81 (2.37%) of these dislocated septa could easily be replaced by a closed reposition. In 29 (0.86% of 3425) newborns, repositioning the deviated nasal structure was impossible, thus leaving the baby with a deviated septum and bony pyramids like the neonate in Fig.35.7 (left) who presents nasal deviation to the left, oblique columella and asymmetrical nostrils. Typically is also the oblique bony pyramid with asymmetrical slope and length on both sides.
Over a period of 11–12years, 14 children out of 29 newborns with non-replaceable nasal deviation were prospectively followed by the author and a second otorhinolaryngologist [37]. No child had a history of nasal trauma in the meantime. The results show that the newborns’ noses, which deviated intrauterinely due to some unknown reasons, did not spontaneously restore in each case. Nine children had a com­pletely straight bony pyramid, symmetric nos-
35.3.4 Congenital Nasal Deviations
trils and reported subjectively normal breathing. Four children had proven nasal allergy and pre-
The histological depiction of a slight septal devi­ation in a newborn without signs of an acute
sented bilateral hypertrophy of the inferior tur­binates. Eight of the nine septa showed slight
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