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12 Physiology andPathophysiology ofSneezing andItching: Mechanisms oftheSymptoms
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What is the benet of photic sneeze reex? Photic sneezing reex exists in animals for which the smell sensation is vital to survive and can be used to clean the nasal cavity. Animals such as cats and dogs sneeze largely through their nose, while the adults sneeze through their mouth. The reex arc may also be useful to a limited extent in human beings when it is considered that the nasal respiration is dominant in the neonatal period. Babies have no other way to get rid of the annoy­ing little tickle caused by normal mucus. Young children sometimes have more disgusting ways of dealing with that sensation, but babies just sneeze often with the help of photic sneeze reex. In conclusion, photic sneeze reex, which can lead the drivers to have accidents following a sudden exposure to sunlight at the end of a long tunnel, or can cause a plane crash by inactivating the masks of jet pilots, can be considered to be an annoying “holdover” of evolution [51, 52].
Hyden and Arlinger examined whether the tickling inside the nose prior to photic sneeze in cases is associated with a recordable local activ­ity or not, and they stated that no reproducible electrical activity could be recorded [53].
Langer etal. designed a study to study the cor­tical keystones of photic sneezing, and revealed that photic sneeze might be the result of superior sensitivity to visual stimuli in the visual cortex and of co-activation of somatosensory areas [54]. The ‘photic sneeze reex’ is therefore not a clas­sical reex that occurs only at a brainstem or spi­nal cord level but, in contrast to many theories, involves also specic cortical areas.
Sevillano et al. assessed the ocular involve­ment in the pathophysiology of ACHOO syn­drome and stated that a dominant autosomal inheritance with mild penetrance was demon­strated, with 67% of the studied subjects showing some degree of prominent corneal nerves [55].
Wand etal. performed a genome-wide asso­ciation study on photic sneeze reex in the Chinese population to uncover the underlying genetic markers in a Chinese population of 3417 individuals, and reproducibly identied both a replicative rs10427255 on 2q22.3 and a novel locus of rs1032507 on 3p12.1in various effect models [56].
There is no recognized management for pho­tic sneeze reex; however, Bobba etal. offered a practical approach to minimizing the PSR by uti­lizing the Philtral Pressure Technique [57]. This involved rm digital pressure applied by the patient’s index nger transversely to the skin of the sub-philtral region, directed posterosuperi­orly onto the maxilla.
12.3.3 Physical Stimulants
oftheTrigeminal Nerve
Physical or mechanical stimulants in the innerva­tion zone of the trigeminal nerve may trigger sneezing reex. Some of these stimulants include pulling hair, tearing off eyebrows, or orbital injections administered frequently during ocular surgery under local anesthesia [58, 59].
12.3.4 Central Nervous System
Pathologies
The lateral medullary syndrome (LMS), or Wallenberg’s syndrome, often results from occlu­sion or dissection of the vertebral artery. Vertebral artery dissection has been blamed on many dif­ferent life events, such as sneezing [60]. Paroxysmal sneezing at the onset of LMS is usu­ally interpreted as a cause, since a violent sneeze could potentially result in a vertebral artery dis­section causing LMS. Due to inactivation of sneezing center in LMS, sneezing cannot occur although the sensation of sneezing is present [6163]. Localization of the human sneeze center was described in a patient with right LMS, ini­tially presenting with violent sneezes and fol­lowed by brief loss of the sneeze reex with eventual recovery [64].
Sneezing may commonly accompany temporal lobe and grand mal epilepsy. It may be observed during the aura prior to an epileptic seizure or it may develop as an autonomic reexive response during the seizure as well [65, 66]. Beverwyck commented upon the analogy of the epileptic sei­zure with hiccups and sneezing and noted that the physiological and anatomical basis for such a
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hypothesis remained to be unexplained [67]. In the mid-nineteenth century, Jackson used the term epilepsy “as the name for occasional, sudden, excessive, rapid and local discharges of grey mat­ter” [68]. Jackson further commented upon the healthy and yet random discharge and concluded that “a sneeze is a sort of healthy epilepsy.”
12.3.5 Psychogenic (Intractable) Sneezing
Intractable sneezing, rst described by Shilkrel in 1949, is a rare pathological condition that has been detected in more than 50 cases in literature up to present [6971]. Kanner referred to a 13-year-old girl who had incessant sneezing for over 2months and whose progress was followed by a daily newspaper communique [72]. A diag­nosis of hysteria was made and subsequent psy­chotherapy eliminated the sneezing. Yater referred to similar explosive repetitious episodes and considered them to be a sort of imitation of the true act of sneezing [73].
Psychogenic intractable sneezing occurs mainly in adolescent girls for which a cause may not be found. Organic lesions or causes should always be carefully excluded [71]. Patients are usually refractory to various medications and have an otherwise unremarkable extensive workup [74, 75]. Inspiratory phase is quite short and the amount of nasal mucosal secretion expelled very low. Eyes may remain open during sneezing. It usually develops due to psychogenic factors and is refractory to medical treatment [76]. Approximately 25% of the reported cases resolve without any form of treatment, except counseling of the patient and family [71]. Psychogenic sneezing responds well to psycho­logical measures such as psychotherapy, biofeed­back, relaxation exercises, supportive psychotherapy (i.e., explanation of nature of ill­ness, suggestion to overcome symptoms), and behavior therapy (reward when there is symptom reduction, aversion therapy, hypnosis, and relax­ation). The role of anxiolytic drugs lies in reduc­ing underlying anxiety and making the patient more amenable to psychotherapy [77].
Medically unexplained physical symptoms usually carry diagnostic difculties for the physi­cians [71]. The most important factors that increase these diagnostic difculties are the pos­sibility of an underlying physical illness and the uncertainty encountered as to how far the investi­gations for physical causes should go. It was determined that in some somatization patients, organic pathologies were revealed during follow­ up. Paradoxically, it is known that repetitive and advanced investigations for any organic etiology in conversion disorder may increase the anxiety and doubts in the family and thus prolong the duration of the illness. In conclusion, one must not assume that every case of paroxysmal sneez­ing is of psychogenic origin. Due to the nature of such a disorder, these patients should undergo medical evaluations before a psychogenic cause is even considered.
12.3.6 Snatiation* Reex
An uncontrollable sneezing attack developing as a result of stretching of the stomach following an excessive nutrition is rst described by Teebi etal. as a reex with autosomal dominant inheri­tance pattern [78]. The mechanism of develop­ment is unknown. Snatiation* is a combination of the words “sneeze” and “satiation.” Snatiation also stands for “Sneezing Noncontrollably At a
Tune of Indulgence of the Appetite-a Trait Inherited and Ordained to be Named” [79]. This
abbreviation was supposed to facilitate the future cases to be evaluated in the same class. Recently, two patients have been reported, who state that several members of their family sneeze on a full stomach [80]. This report doubles the number of families with snatiation reex in the medical literature.
12.3.7 Sexual Ideation or Orgasm
An association between sexual excitement and sneezing was rst described in the nineteenth century [49, 81] followed by a young German otolaryngologist who developed a theory of
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“nasal reex neurosis” due to the nding of erec­tile tissue in both nasal mucous membranes and genital areas [82, 83]. The rst report of this phe­nomenon in the literature describes a 69-year-old man who complains of severe sneezing immedi­ately following orgasm, with no associated psy­chiatric morbidity [84]. Stromberg in 1975 and Korpas in 1979 described male orgasm as a pre­cipitant for the sneeze reex [85, 86]. Bhutta described a middle-aged man with uncontrollable ts of sneezing with sexual thought. The patient had no other rhinological symptoms and psychi­atric morbidity [87]. Bhutta et al. performed a search of Internet “chat rooms” and found 17 people of both sexes reporting sneezing immedi­ately upon sexual ideation and three people after orgasm. Although Internet reports do not give an accurate incidence, their ndings do suggest that it is much more common than recognized. One year later, Bhutta and Maxwell revealed their experience on internet-based media or by sponta­neous contact with the authors that sneezing induced by sexual ideation reported in additional 146 cases [80].
12.4 Diagnosis, Dierential Diagnosis, andManagement ofRhinitis
The evaluation of a patient with sneezing should be individualized according to the duration and severity of the symptom. Laboratory tests are not necessary in the majority of patients, since the diagnosis is usually obvious from the history and physical examination.
It should be remembered that the history of the patient is the most important and determining stage for the diagnosis [88]. The patient should be asked what his/her main complaint is; the duration and frequency of the symptoms like nasal discharge, stufness, and pruritus if pres­ent; whether the nasal discharge or stufness is present on one side or both, perennial or sea­sonal; whether he/she has allergic complaints, past trauma, past nasal surgery history, known diseases, and drugs used; and also how these symptoms effect the quality of life. In female
patients it is also important to ask whether she is pregnant or on oral contraceptives [36]. One of the most common signs of allergic rhinitis in children is a horizontal creasing over the nasal tip. This physical examination sign develops as a result of habitual rubbing, which is also called allergic salute, after a duration of at least 2years, a repeated action in order to relieve pruritus and improve respiration. This habit may turn into facial grimacing in adulthood for social reasons. Allergic shiner, on the other hand, is permanent pigmentation on the skin of lower eyelid which present as dark circles at the beginning stage. It develops due to subcutaneous hemosiderin through a capillary leak during periorbital venous stasis as a result of nasal mucosal congestion. Dennie–Morgan folds are short semilunar lines or folds found below the inferior eyelid. These lines develop due to venous blood retention cause by continuous spasm of Müller’s muscle under the inferior eyelid. Silky long eyelashes are another outstanding concomitant sign of allergy. Clinical examination including anterior rhinos­copy and nasal endoscopy provides large infor­mation about pathologies related to septum and lateral nasal wall. Allergy is prediagnosed with medical history and physical examination. If the patient has a medical history and complaints that are compatible with allergy, in vivo (prick test, SET, scratch test) and/or invitro (serum-specic IgE) allergy tests should be performed [89]. The skin prick test is the most common epidermal test. A positive allergen skin test that is compati­ble with the medical history and ndings of phys­ical examination should be assumed to be signicant [90]. RAST (radioallergosorbent test) and ELISA (enzyme-linked immunosorbent assay) tests measure the amount of allergen­specic IgE antibodies. Since there is no risk of systemic reactions during the application of these tests, they can safely be performed on pregnant women, on patients with a past history of sys­temic reaction, during measuring the sensitivity to antigens with a high risk of systemic reaction, on patients with skin diseases, on people who use drugs that may affect the prick skin test results, and in medicolegal cases where objective data are needed and also on children. The changes that
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develop due to gradually increasing doses of the allergen are followed by nasal provocation test. This test is performed when objective data are needed for occupational rhinitis, and it is rather used for scientic studies. Nasal cytology is not a diagnostic method performed for routine clinical practice and considered as an evaluation that does not provide a sufcient support alone [91]. The use of acoustic rhinometry and rhinomanom­etry, which are the most common objective nasal airway tests, is conned because they have high costs and is time demanding in terms of applica­tion and interpretation [92]. Mucociliary function may be evaluated for differential diagnosis in patients with rhinitis [93]. Radiological examina­tion is not necessary in a patient prediagnosed with rhinitis as long as an additional pathology is not suspected.
The treatment of persistent or recurring sneez­ing should be directed at the cause whenever pos­sible. The best treatment in patients with allergic rhinitis is to avoid the allergen [94]. Medical treatment or when needed, even immunotherapy when needed, is used in patients who do not ben­et from avoidance or environmental control [9598]. Some patients may benet from adjunc­tive surgical treatment. The management of com­mon cold and inuenza is symptomatic. Decongestants, antipyretics, bed rest, and increased uid intake are recommended. Systemic antibiotics are preferred in patients who develop bacterial infections secondary to a viral infection while agent-specic antibiotic treat­ment is applied in those who develop rhinitis sec­ondary to specic bacteria. It is vital to diagnose the patient and initiate the treatment immediately, particularly in fulminant fungal infections. The initial stage in the treatment of the patients with NARES is avoiding the irritant environmental conditions. Medical treatment is considered in case the initial stage fails to succeed. The success of steroids in early phases decreases in long-term administrations due to decreased steroid recep­tors on eosinophils. Oral and topical deconges­tants may be used adjunctive to steroid therapy. Capsaicin, a substance isolated from chili pepper extract, has an initial stimulating effect on C receptors which turns into an inhibiting effect
following repetitive applications. Antihistamines are of no use and treatment of vasomotor rhinitis is palliative. Oral and topical decongestants can be applied. Topical corticosteroids are not always benecial. Ipratropium bromide, which prevents the secretions from serous and seromucous glands inhibiting the cholinergic system, may be effective. Antihistamines are of no use. In the treatment of gestational rhinitis, medication should denitely be avoided for the rst 10weeks, and the treatment should denitely be applied with obstetric advice in the following periods. Isotonic saline sprays may be useful for pregnant women due to their humidifying and mucosal cleaning effects. The rst line medical treatment for allergic rhinitis in pregnant women is cromo­lyn sodium, a mast cell stabilizer. Beclomethasone and triamcinolone are the topical steroids of choice for those who do not benet from cromo­lyn sodium. The safest antihistamine during pregnancy is chlorpheniramine and the safest oral decongestant is pseudoephedrine. In the manage­ment of rebound rhinitis, the inducing drug should be discontinued and oral or parenteral corticosteroids should be administered in order to relieve the patient’s complaints, and the treat­ment should be supported with topical nasal cor­ticosteroids. Surgery may be necessary if irreversible changes have developed in the infe­rior conchae. The purpose of the treatment in geriatric rhinitis should be to provide sufcient intracellular moisture. For this purpose, it is appropriate to humidify the nasal mucosa with solutions including a combination of isotonic solution and glycerine and to add guaifenesin to treatment which stimulates the submucosal glands. Isotonic solutions can be combined with glycerine for the initial management of atrophic rhinitis. Other solutions can be antibiotherapy, estrogen support, vitamins A and D administra­tion, iron support, or corticosteroid administra­tion. It has also been recommended to practice surgical closure of one or both nostrils for a period of 1year, or surgical procedures to narrow the nasal cavity have been recommended. Avoiding irritant substances should be the initial approach for the management of occupational or irritant-induced rhinitis (Table12.2).
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Table 12.2 Differential diagnosis of rhinitis in terms of history and laboratory tests
Feature Allergic rhinitis Infectious rhinitis NARES Vasomotor rhinitis Onset of symptoms Seasonal/perennial Seasonal Perennial Perennial Symptoms Sneezing Sneezing Sneezing Sneezing
Nasal stufness Nasal stufness Nasal stufness Nasal stufness Nasal pruritus Nasal discharge Nasal discharge Nasal discharge Nasal discharge Fever Postnasal drip
Postnasal drip Myalgia Triggering allergen Ye s No No No Triggering irritant Yes No Ye s Yes Allergy tests Positive Negative Negative Negative Nasal cytology Eosinophilia Neutrophilia Eosinophilia Rare eosinophilia
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12.5 Complications ofSneeze Reex
Since the symptoms of majority of upper respira­tory tract infections include cough and sneezing, numerous particles disperse into the air during the course of these diseases. The most important complication of sneezing that affects public health is spread of droplet infections, tuberculo­sis in particular. The incidence of tuberculosis, which was taken under control through the improvement of efcient treatments in the second half of the twentieth century, began to increase again due to certain factors including the outburst of HIV infection, the decrease in the importance given to disease control, and poverty [99, 100].
Gwaltmey et al. have determined that the intranasal pressure increases up to 176 mmHg during sneezing with the mouth and the nostrils closed [101]. Complications pertaining to this high pressure have been reported in literature. These complications include acute aortic dissec­tion, cerebral venous thrombosis, loss of hearing due to fracture footplate, abortus, orbital emphy­sema, pneumocephalus, acute wide-angle glau­coma, pneumatocele of the lacrimal sac, intimal tear of the arteriovenous stula, retinal hemor­rhage, and costal fracture reported in a patient with osteoporosis [102109].
12.6 Conclusion
Sneezing is a phenomenon that is common to all humans and is widespread in the animal kingdom as well. It may play an important role in maintain-
ing health in ways that we do not currently under­stand. Sneezing, which cannot consciously be controlled, is a protective reex for the body during which facial, pectoral, and abdominal muscles function concordantly maintaining the respiration. It is rarely a sign of serious illness or impending disaster as feared by previous generations. On the other hand, it can be remarkably annoying. A thor­ough knowledge of this reex can be a valuable aid in the diagnosis of other concomitant diseases.
Conict of Interest The author has no nancial relation­ship with a commercial entity that has an interest in the subject of this manuscript.
References
1. Songu M, Cingi C.Sneeze reex: facts and ction. Ther Adv Respir Dis. 2009;3:131–41.
2. Aristotle. Problems, Book XXXIII (trans: Rackham H, Hett WS). Cambridge: Harvard University Press;
1994.
3. Disraeli I. Curiosities of literature. Cambridge: Riverside Press; 1864.
4. Prioreschi P. A history of medicine, Roman medi­cine, vol. III.Omaha: Horatius Press; 1998.
5. Ovesen L.A regular contribution from Lars Ovesen, which we hope will help the busy scientist in keep­ing up with the literature ne arts. Eur J Cancer Prev. 2003;12:239–40.
6. Knowlson ST. The origins of popular superstitions and customs. Forgotten Books. London: T. Werner Laruier Clifford’s Inn; 1910.
7. Klimek L, Riechelmann H, Saloga J, et al. Anatomie, Physiologie und Immunologie der Nasenschleimhaut, spezische und unspezische Abwehrmechanismen. In: Klimek L, Riechelmann H, Saloga J, Mann W, Knop J, editors. Allergologie und Umweltmedizin. Stuttgart-New York: Schattauer; 1997.
142
https://t.me/medicina_free
M. Songu and T. M. Onerci
8. Kovacs I, Ludany A, Koszegi T, et al. Substance P released from sensory nerve endings inuences tear secretion and goblet cell function in the rat. Neuropeptides. 2005;39:395–402.
9. Nishino T. Physiological and pathophysiological implications of upper airway reexes in humans. Jpn J Physiol. 2000;50:3–14.
10. Wallois F, Macron JM, Jounieaux V, etal. Trigeminal afferences implied in the triggering or inhibition of sneezing in cats. Neurosci Lett. 1991;122:145–7.
11. Widdicombe JG. Nasal pathophysiology. Respir Med. 1990;84(Suppl A):3–9.
12. Torebjork HE, Hallin RG. Perceptual changes accompanying controlled preferential blocking of A and C bre responses in intact human skin nerves. Exp Brain Res. 1973;16:321–32.
13. Ader R, Cohen N, Felten D.Psychoneuroimmunology: interactions between the nervous system and the immune system. Lancet. 1995;345:99–103.
14. Hsieh JC, Hagermark O, Stahle-Backdahl M, etal. Urge to scratch represented in the human cerebral cortex during itch. J Neurophysiol. 1994;72:3004–8.
15. Pfaar O, Raap U, Holz M, etal. Pathophysiology of itching and sneezing in allergic rhinitis. Swiss Med Wkly. 2009;139(3–4):35–40.
16. Schmelz M, Schmidt R, Bickel A, et al. Specic C-receptors for itch in human skin. J Neurosci. 1997;17:8003–8.
17. Suranyi L. Localization of the sneeze center. Neurology. 2001;57:161.
18. Hummel T, Doty RL, Yousem DM.Functional MRI of intranasal chemosensory trigeminal activation. Chem Senses. 2005;30(Suppl 1):i205–6.
19. Sarin S, Undem B, Sanico A, etal. The role of the nervous system in rhinitis. J Allergy Clin Immunol. 2006;118:999–1016.
20. Batsel HL, Lines AJ.Neural mechanisms of sneeze. Am J Phys. 1975;229:770–6.
21. Setzen S, Platt M.The dangers of sneezing: a review of injuries. Am J Rhinol Allergy. 2019;33:331–7.
22. Singh NK, Kumar N, Singh AK. Physiology of disease transmission of respiratory tract infection: a narrative review. Infect Disord Drug Targets. 2021;21(6):e170721188930.
23. Bousquet J, van Cauwenberge P, Khaltaev N, The ARIA Workshop Group, World Health Organization. Allergic rhinitis and its impact on asthma. J Allergy Clin Immunol. 2001;108(Suppl):147–334.
24. Cingi C, Topuz B, Songu M, et al. Prevalence of allergic rhinitis among the adult population in Turkey. Acta Otolaryngol. 2010b;130:600–6.
25. Ozdoganoglu T, Songu M. The burden of aller­gic rhinitis and asthma. Ther Adv Respir Dis. 2012;6:11–23.
26. Ozdoganoglu T, Songu M, Inancli HM. Quality of life in allergic rhinitis. Ther Adv Respir Dis. 2012;6:25–39.
27. Kim D, Baraniuk JN. Neural aspects of allergic rhinitis. Curr Opin Otolaryngol Head Neck Surg. 2007;15:268–73.
28. Klimek L, Schäfer D.Wirkung von Substanz-P in
29. Mosimann BL, White MV, Hohman RJ, et al.
30. Levi-Montalcini R.The nerve growth factor 35 years
31. Raap U, Fokkens W, Bruder M, etal. Modulation of
32. Dykewicz MS, Fineman S, Skoner DP, et al.
33. Fairbanks DNF, Kaliner M. Nonallergic rhini-
34. Stevens HE. Allergic and inammatory aspects
35. King HC, Mabry R.A practical guide to the manage-
36. Incaudo GA. Diagnosis and treatment of allergic
37. Cingi C, Ozdoganoglu T, Songu M. Nasal obstruc-
38. Imamura T, Kambara T. Substance P as a potent
39. Kira S, Nogami Y, Taketa K, etal. Size-selective
40. Kitajiri M, Kubo N, Ikeda H, etal. Effects of topical
41. Geppetti P, Fusco BM, Marabini S, etal. Secretion,
42. Canning BJ.Neurology of allergic inammation and
43. Collie WR, Pagon RA, Hall JG, et al. ACHOO
44. Sedan J. Photosternutatory reex. Rev
45. Morris HH 3rd. ACHOO syndrome: prevalence and
der Nasenschleimhaut. Allergologie. 1996;19:524.
Substance P, calcitonin gene-related peptide, and vasoactive intestinal peptide increase in nasal secre­tions after allergen challenge in atopic patients. J Allergy Clin Immunol. 1993;92:95–104.
later. Science. 1987;237:1154–62.
neurotrophin and neurotrophin receptor expression in nasal mucosa after nasal allergen provocation in allergic rhinitis. Allergy. 2008;63:468–75.
Diagnosis and management of rhinitis: complete guidelines of the joint task force on the parameters in allergy, asthma and immunology. Ann Allergy Asthma Immunol. 1998;81:478–518.
tis and infection. In: Cummings CW, Fredrickson JM, Harker LA, Krause CJ, et al., editors. Otolaryngology– head and neck surgery. St. Louis: Mosby Year Book; 1998.
of chronic rhinosinusitis. J Otolaryngol. 1991;20:395–9.
ment of nasal and sinus disorders. 1st ed. NewYork: Thieme; 1993.
rhinitis and sinusitis during pregnancy and lactation. Clin Rev Allergy Immunol. 2004;27:159–77.
tion as a drug side effect. Ther Adv Respir Dis. 2011;5:175–82.
stimulator of sneeze responses in experimental allergic rhinitis of guinea pigs. Agents Actions. 1992;37:245–9.
sampling of oil mist in air and subjective symp­toms among machine workers. Ind Health. 1997;35:394–8.
capsaicin on autonomic nerves in experimentally­induced nasal hypersensitivity. An immunocytochem­ical study. Acta Otolaryngol Suppl. 1993;500:88–91.
pain and sneezing induced by the application of cap­saicin to the nasal mucosa in man. Br J Pharmacol. 1988;93:509–14.
rhinitis. Curr Allergy Asthma Rep. 2002;2:210–5.
syndrome (autosomal dominant compelling helio­ophthalmic outburst syndrome). Birth Defects Orig Artic Ser. 1978;14:361–3.
Otoneuroophthalmol. 1954;26:123–6.
inheritance. Cleve Clin J Med. 1987;54:431–3.
12 Physiology andPathophysiology ofSneezing andItching: Mechanisms oftheSymptoms
https://t.me/medicina_free
143
46. Everett HC.Sneezing in response to light. Neurology. 1964;14:483–90.
47. Beckman L, Nordenson I. Individual differences with respect to the sneezing reex: an inherited phys­iological trait in man? Hum Hered. 1983;33:390–1.
48. Eckhardt LB, McLean JM, Goodell H.The genesis of pain from the eye. Assoc Res Nerv Ment Dis Proc. 1943;23:209–17.
49. Watson WS.Diseases of the nose and its accessory cavities. London: Lewis; 1875.
50. Brubaker AP. The physiology of sneezing. JAMA. 1919;73:585–7.
51. Benbow EW. Practical hazards of photic sneezing. Br J Ophthal. 1991;75:447.
52. Breitenbach RA, Swisher PK, Kim MK, etal. The photic sneeze reex as a risk factor to combat pilots. Mil Med. 1993;158:806–9.
53. Hydén D, Arlinger S. On light-induced sneezing. Eye (Lond). 2009;23:2112–4.
54. Langer N, Beeli G, Jäncke L.When the sun prickles your nose: an EEG study identifying neural bases of photic sneezing. PLoS One. 2010;5:e9208.
55. Sevillano C, Parata-Fernández A, Rodriguez­Lopez V, etal. A curious fact: photic sneeze reex. Autosomical dominant compelling helio- ophthalmic outburst syndrome. Arch Soc Esp Oftalmol. 2016;91:305–9.
56. Wang M, Sun X, Shi Y, Song X, Mi H. A genome­wide association study on photic sneeze reex in the Chinese population. Sci Rep. 2019;9:4993.
57. Bobba S, Spencer SKR, Fox OJK, etal. Management of the photic sneeze reex utilising the philtral pres­sure technique. Eye (Lond). 2019;33:1186–7.
58. Sekizawa SI, Ishikawa T, Sant’Ambrogio G. Asymmetry in reex responses of nasal mus­cles in anesthetized guinea pigs. J Appl Physiol. 1998;85:123–8.
59. Wallois F, Bodineau L, Macron JM, et al. Role of respiratory and non-respiratory neurones in the region of the NTS in the elaboration of the sneeze reex in cat. Brain Res. 1997;768:71–85.
60. Schievink WI. Spontaneous dissection of the carotid and vertebral arteries. N Engl J Med. 2001;344:898–906.
61. Bernat JL, Suranyi L.Loss of ability to sneeze in lat­eral medullary syndrome. Neurology. 2000;55:604.
62. Hersch M.Loss of ability to sneeze in lateral medul­lary syndrome. Neurology. 2000;54:520–1.
63. Martin RA, Handel SF, Aldama AE. Inability to sneeze as a manifestation of medullary neoplasm. Neurology. 1991;41:1675–6.
64. Seijo-Martinez M, Varela-Freijanes A, Grandes J, etal. Sneeze related area in the medulla: localiza­tion of the human sneeze center? J Neurol Neurosurg Psychiatry. 2006;77:559–61.
65. Peneld W, Jasper H. Epilepsy and the functional anatomy of the human brain. Boston: Little, Brown & Company; 1954.
66. Peneld W, Kristiansen K.Epileptic seizure patterns: a study of the localizing value of initial phenomena
in focal cortical seizures. Springeld: Charles C Thomas; 1951.
67. Temkin O.The falling sickness: a history of epilepsy from the Greeks to the beginnings of modern neurol­ogy. Baltimore: Johns Hopkins Press; 1945.
68. Jackson JH.On the scientic and empirical investiga­tion of epilepsies. In: Taylor J, editor. Selected writ­ings of John Hughlings Jackson, vol. 1. NewYork: Basic Books; 1958.
69. Bhatia MS, Khandpal M, Srivastava S, et al. Intractable psychogenic sneezing: two case reports. Indian Pediatr. 2004;41:503–8.
70. Shilkrel HH. Psychogenic sneezing and yawning. Psychosom Med. 1949;11:127–8.
71. Sulemanji MN, Kanbur NO, Derman O, et al. Intractable sneezing: is it always psychogenic? Turk J Pediatr. 2011;53(2):225–8.
72. Kanner L. Child psychiatry. 3rd ed. Springeld: Charles C.Thomas; 1957.
73. Yater WM, Barton WM. Symptom diagnosis: regional and general. 4th ed. NewYork: D.Appleton­Century Company; 1942.
74. Bergman GE.Psychogenic intractable sneezing in children. J Pediatr. 1984;105:496–8.
75. Lin TJ, Maccia CA, Turnier CG. Psychogenic intractable sneezing: case reports and a review of treatment options. Ann Allergy Asthma Immunol. 2003;91:575–8.
76. Gopalan P, Browning ST. Intractable paroxysmal sneezing. J Laryngol Otol. 2002;116:958–9.
77. Guner SN, Gokcen C, Gokturk B, etal. Haloperidol: a possible medication for the treatment of exacer­bation of intractable psychogenic sneezing. Int J Pediatr Otorhinolaryngol. 2010;74(10):1196–8.
78. Teebi AS, Al-Saleh QA.Autosomal dominant sneez­ing disorder provoked by fullness of stomach (let­ter). J Med Genet. 1989;26:539–40.
79. Hall JG.The snatiation reex (letter). J Med Genet. 1990;27:275–8.
80. Bhutta MF, Maxwell H. Further cases of unusual triggers of sneezing. J R Soc Med. 2009;102:49.
81. Mackenzie JN.Irritation of the sexual apparatus as an etiological factor in the production of nasal dis­ease. Am J Med Sci. 1884;87:360–5.
82. Jones E. The life and work of Sigmund Freud. London: Penguin Books; 1974.
83. Young AR.Freud’s friend Fliess. J Laryngol Otol. 2002;116:992–5.
84. Anonymous. Paroxysmal sneeze following orgasm. JAMA. 1972;219:1350–1.
85. Korpas J, Tomori Z. Cough and other respiratory reexes. In: Bollinger CT, editor. Progress in respi­ratory research, vol. 23. Basel: Karger; 1979.
86. Stromberg BV. Sneezing: its physiology and man­agement. Eye Ear Nose Throat Mon. 1975;54:49–53.
87. Bhutta MF, Maxwell H.Sneezing induced by sexual ideation or orgasm: an under-reported phenomenon. J R Soc Med. 2008;101:587–91.
88. Kramer MF.Diagnosis of persistent rhinitis. MMW Fortschr Med. 2006;148:37–9.
144
https://t.me/medicina_free
M. Songu and T. M. Onerci
89. Settipane GA, Klein DE. Non-allergic rhinitis: demography of eosinophils in nasal smears, blood eosinophil counts and IgE levels. N Engl Reg Allergy Proc. 1985;6:363–6.
90. Skoner DP. Allergic rhinitis: denition, epidemiol­ogy, pathophysiology, detection, and diagnosis. J Allergy Clin Immunol. 2001;108:2–8.
91. Scadding GK. Non-allergic rhinitis: diagnosis and management. Curr Opin Allergy Clin Immunol. 2001;1:15–20.
92. Galen BA. Differential diagnosis: rhinitis. Lippincotts Prim Care Pract. 1997;1(2):129–41.
93. Shaari J, Palmer JN, Chiu AG, etal. Regional analy­sis of sinonasal ciliary beat frequency. Am J Rhinol. 2006;20:150–4.
94. Cingi C, Unlu HH, Songu M, etal. Seawater gel in allergic rhinitis: entrapment effect and mucociliary clearance compared with saline. Ther Adv Respir Dis. 2010c;4:13–8.
95. Bousquet J, Bachert C, Canonica GW, ACCEPT-1 study group, etal. Efcacy of desloratadine in inter­mittent allergic rhinitis: a GA(2)LEN study. Allergy. 2009;64:1516–23.
96. Bousquet J, Bachert C, Canonica GW, ACCEPT-2 Study Group, etal. Efcacy of desloratadine in per­sistent allergic rhinitis– a GA2LEN study. Int Arch Allergy Immunol. 2010;153:395–402.
97. Cingi C, Cakli H, Yaz A, et al. Phototherapy for allergic rhinitis: a prospective, randomized, single­blind, placebo-controlled study. Ther Adv Respir Dis. 2010a;4:209–13.
98. Gunhan K, Unlu H, Yuceturk AV, etal. Intranasal steroids or radiofrequency turbinoplasty in persis­tent allergic rhinitis: effects on quality of life and objective parameters. Eur Arch Otorhinolaryngol. 2011;268:845–50.
99. Adler JJ, Rose DN. Transmission and pathogen­esis of tuberculosis. In: Rom WN, Garay SM, edi­tors. Tuberculosis. New York: Little, Brown and Company; 1996.
100. Centers for Disease Control and prevention. Guidelines for preventing the transmission of Mycobacterium tuberculosis in health-care facilities. MMWR. 1994;43:1–132.
101. Gwaltney JM Jr, Hendley JO, Phillips CD, et al. Nose blowing propels nasal uid into the paranasal sinuses. Clin Infect Dis. 2000;30:387–91.
102. Baydin A, Nural MS, Guven H, etal. Acute aortic dissection provoked by sneeze: a case report. Emerg Med J. 2005;22:756–7.
103. Birkent H, Durmaz A, Hidir Y, etal. Sneezing-related orbital emphysema and pneumocephalus treated with transnasal endoscopic surgery. J Otolaryngol Head Neck Surg. 2008;37:E167–9.
104. Fonseca AC, Ferreira JJ, Albuquerque L, et al. Sneeze as a precipitating factor of cerebral venous thrombosis. Eur J Neurol. 2007;14:7–8.
105. Gonzalez F. Orbital emphysema after sneezing. Ophthal Plast Reconstr Surg. 2005;21:309–11.
106. Gupta A, Dogra PM, Singh B, etal. Arteriovenous stula intimal tear: think before you sneeze. Ther Apher Dial. 2010;14:124.
107. Rochels R, Bleier R, Nover A. Compression pneumatocele of the lacrimal sac. Klin Monatsbl Augenheilk. 1989;195:174–6.
108. Sharir M, Huntington AC, Nardin GF, etal. Sneezing as a cause of acute angle-closure glaucoma. Ann Ophthalmol. 1992;24:214–5.
109. Whitehead E. Sudden sensorineural hearing loss with fracture of the stapes footplate following sneez­ing and parturition. Clin Otolaryngol Allied Sci. 1999;24:462–4.
The Dry Nose
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RainerK.Weber, TanjaHildenbrand, DetlefBrehmer, andJochenA.Werner
13
Core Messages
• An unequivocal denition of the dry nose (DN) is not available. Symptoms range from the purely subjective sensation of a rather dry nose to visible crusting of the (inner) nose (nasal mucosa), and a wide range of combina­tions are met with. Relevant diseases are termed rhinitis sicca anterior, primary and sec­ondary rhinitis atrophicans, rhinitis atrophi­cans with foetor (ozaena) and empty nose syndrome. The diagnosis is based mainly on the patient’s history, inspection of the nose, endoscopy of the nasal cavity, sinuses and nasopharynx, with CT, allergy testing and
R. K. Weber (*) · J. A. Werner Department of Otorhinolaryngology, Head and Neck Surgery, Rhinology Center Marburg, University Hospital Marburg UKGM, Marburg, Germany e-mail: weber@uk-gm.de; jochen.werner@uk-gm.de
T. Hildenbrand Department of Otorhinolaryngology/ENT Department, University Hospital Freiburg, Freiburg, Germany e-mail: tanja.hildenbrand@uniklinik-freiburg.de
D. Brehmer Private ENT Clinic Goettingen, Faculty of Health/ School of Medicine, University Witten/Herdecke, Goettingen, Germany e-mail: d.brehmer@hno-praxis-goettingen.de
microbiological swabs being performed where indicated.
• Treatment consists of the elimination of pre­disposing factors, moistening, removal of crusts, avoidance of injurious factors, care of the mucosa, treatment of infections and, where applicable, correction of overlarge air space.
13.1 Symptoms
One of the chief functions of the nose is to warm and moisten the inspired air, while another is to recover the water in the expired air [1].
The nature of the in- and outow of the air
within the nasal cavity is of decisive importance for this air-conditioning feature. In this context, optimal distribution of the inspired air over the nasal turbinates ensuring intimate contact of the air with the surface-moist mucosal membrane is essential.
The expression dry nose (DN) has not been
unambiguously dened. In the main, it is based on relevant anamnestic patient information. ENT specialists often employ the term rhinitis sicca, although here, too, a clear denition is lacking. Symptoms range from the purely subjective sen­sation of a somewhat dry nose to visible crusting of the nose, and a wide range of combinations are possible:
© 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,
https://doi.org/10.1007/978-3-031-12386-3_13
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R. K. Weber et al.
• Sensation of dryness in the nose.
• Itching and mild burning sensation.
• Nasal obstruction.
• Crusting, scabs and ‘bogies’, possibly associ­ated with an (unpleasant) smell.
• Epistaxis.
• Diminished sense of smell.
13.2 Aetiology
Possible causes of dry nose include a variety of diseases, external and internal factors and envi­ronmental conditions:
• Local mechanical irritation.
• Climatic or environmental factors.
– Dry room or environmental air (relative
humidity <50%). – Heated room or hot environment. – Long-distance ights.
• Workplace conditions. – Dry air and clean-room condition [2]. – Cold and heat. – Dusty conditions (e.g. grinding/polishing
of plaster, granite, chalk, cement, wood arsenic, nickel carbonyl, tobacco smoke).
• Drugs (cocaine).
• Side effects of medications (see Table13.1).
• Supportive nasal administration of oxygen [3].
• Symptoms of other diseases (granulomatous, infectious, rheumatic and immunological disorders).
– Wegener’s granulomatosis, sarcoidosis,
tuberculosis, syphilis and leprosy (Fig.13.1).
• Wound healing phase after endonasal sinus surgery and surgery on the nose.
• Anatomical changes to the outer and inner nose, with modication of normal airow.
• Allergic rhinitis, in particular, house dust mites and moulds.
• Permanent sequelae of surgery on the nose and paranasal sinuses.
• Sequelae of head and neck radiotherapy.
• Patients with obstructive sleep apnoea (OSA) or continuous positive airway pressure (CPAP) treatment in sleep apnoea patients [4]. Moistening led to a reduction in symptoms [5].
• Old age.
Dry nose may be the rst symptom of an
incipient cold with a runny nose; in such a case, however, it is of only limited duration.
Although an increased susceptibility to infec-
tions has frequently been postulated and is patho-
Table 13.1 Medications with the side effect of dry nose
Substance group Generic name Indications Retinoids (1–10%) Isotretinoin Severe forms of acne
Doxepin (tricyclic antidepressant) Methyldopa (1‰–1%) Hypertension (of pregnancy) Sympathomimetics (local)
Antihistaminics, rst generation
Tretinoin Promyelocyte leukaemia
Depressive conditions, anxiety syndrome, mild withdrawal symptoms in alcoholics and drug-dependent persons, agitation, sleep disorders
Dipivefrine (eye) Glaucoma Naphazoline Diverse forms of rhinitis, only short-term use recommended Oxymetazoline Phenylephrine Tetryzoline Tramazoline Xylometazoline Clemastine Urticaria, allergic rhinitis Dimenhydrinate Vertigo, nausea, vomiting Dimethindene Itching, itching dermatoses, allergies Diphenhydramine Difculty getting to sleep, difculty staying asleep Promethazine Agitation in underlying psychiatric illnesses, possibly vomiting,
nausea and sleep disorders
Terfenadine Allergic rhinoconjunctivitis, allergic skin disorders