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evaluateidiopathicsmelldisorders.However,nonspecificalterationsoccurrelativelyfrequentlyevenin
normosmicsubjects,particularlyinoldage,whichoftenrenderstherelationshipbetweenbiopsyfindings
andfunctionalconditionsinconclusive.
91
Note
Biopsiesarehighlyvaluableinexperimentalcontexts,butareoflimitedvalueintheevaluationof
olfactorydisordersinindividualpatients.
HowtoEvaluateParosmiaandPhantosmia
The diagnoses “parosmia”and“phantosmia”are solely baseduponthe patient'sreport.
92
Theymaybe
gradedusingthefollowingsystem:
•Frequencyofoccurrence:daily=1point,otherwise=0points
•Intensity:verystrong=1point,otherwise=0points
•Socialeffects(e.g.,weightloss,significantchangeofhabits):yes=1point,no=0points
Thesumscorerepresentsthedegreeofthedisorder.Findingstosupportthediagnosisofqualitativesmell
disorders are low scores insmellidentificationtests
93
andsmall OBvolumes compared withpatients
withunimpairedolfaction.
81,82
ThelattermayindicatedecreasednumbersofOBinterneurons,resultingin
reducedlateralinhibition,which,inturn,maygeneratequalitativeolfactorydysfunction.
Note
Objectivemethodstovalidateparosmiaandphantosmiaarelacking.Thesedisordersareestablished
solelybaseduponthepatient'shistory.
AssessmentofTasteFunction
Tastestimuliareprocessedviathreecranialnerves:Thefacialnerve,glossopharyngealnerve,andvagal
nerve.Tastereceptorsarepresentinthemouth,oropharynx,andpharyngealportionoftheepiglottis(and
also in the gut!
94
). In addition, the vagal nerve contributes sensations of temperature, texture, and
irritation. The brainstem, thalamus, orbitofrontal cortex, and insula are essentially involved in taste
processing. Gustatorysensitivity decreases with age—if less so than olfactory sensitivity—and, as in
olfaction,isgreaterinwomenthanmen.
Afterestablishingthepatient'shistoryandperformingabasicclinicalexamination(seeChapter5),a
specifictastetestisapplied,eithertotheentireoralcavityorinalocalizedfashion,usingbothnatural
and electrical stimulation. Local testing yields more detailed results, permitting, for example, the
detectionoflateralizedtastedisorders,whereaswhole-mouthtestingsimulateseverydaytasteexperience.
Particularlyincasesofdysgeusia(e.g.,bitterormetallictastes),subjectivereportsoftastesensations
arehighlysignificant,asnoquantitativemethodiscurrentlyavailabletoassessthesetypesofdisorders
(Table6.2).
PsychophysicalWhole-mouthTests
Inwhole-mouthtesting, smallamountsoftastesubstances(e.g.,drops or sprays)areapplied.Patients
distributethesampleintheoralcavity,disgorgeitafterafewseconds,andrinsetheirmouthwithwater.

Suprathreshold testing may be performed with so-called taste sprays, using the natural substances
sucrose(1gin10gaqua;sweet),citricacid(0.5gin10gaqua;sour),sodiumchloride(0.75gin10g
aqua;salty),andquininehydrochloride(0.005gin10gaqua;bitter).Thissuprathresholdprocedureisa
simplescreeningtoolthattestsapatient'sabilitytoidentifytastequalities.
Anotherfrequentlyusedmethodisthethreedropstest.
95
Drops(volume:<0.1mL)ofeitherwateror
atastesolutionareadministeredingroupsofthree,witheachgroupconsistingoftwowaterandonetaste
drop,appliedsuccessivelyinarandomsequence.Thefirstgroupcontainsthelowestconcentrationofthe
tastant.Patientsareaskedtoidentifythetastingdropwithineachgroup.Thetestaimstoassessthetaste
threshold,whichisestablishedastheconcentrationidentifiedthreetimesinarow(forstandardvalues,
pleaseseeref.96).Furthertastetestshavebeensuggested,including“tastetablets,”whichdissolveinthe
oral cavitytoreleasetastesubstances,
97
orwafers impregnatedwith tastesubstances
98
;however,these
testsare not commerciallyavailable. Recent developmentsarebased onsoluble material impregnated
withtastant.
99
Table 6.2Definitionofgustatorydisorders:quantitativedisordersarehighlightedinlightred,andqualitativedisordersindarkred
Diagnosis De scription
Ageusia Totallossofgustatoryfunction
Functionalageusia Significantlyimpairedgustation,includingbothtotallossandminimalresidualperception
Partialageusia Reducedsensitivitytowardonetastequality
Hypogeusia Reducedsensitivity,comparedwithyoung,healthysubjects
Hypergeusia Increasedsensitivity,comparedwithyoung,healthysubjects
Parageusia Abnormalperception,withsensoryinputpresent
Phantogeusia Abnormalperception,withsensoryinputabsent
Note
Anytastetestshouldbeaccompaniedbyabriefsmelltestandviceversa,aspatientsareproneto
mistake aromas for tastesensations, and therefore complainabouttasteproblems insteadofsmell
problems.
PsychophysicalTasteTestsAppliedToSeveralOralSites(LocalTasteTests)
Amonglocaltastetests,thetwo-alternativeforced-choiceprocedureiswidelyused.Patientsareasked
todecidewhichoftwostimuli,presented,forexample,ontheleftandrightside,elicitsatastesensation.
Thismethodmayalsobeusedtoassesstastethresholds.Fig.6.7illustrateslocaltastetests.
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Fig. 6.7a–d Taste tests. (From Hummel T, Welge-Lüssen A. Riech- und Schmeckstorungen: Physiologie, Pathophysiologie und
TherapeutischeAnsatze.Stuttgart:Thieme;2005.)
aLocaltestingwithadequatestimulus:applicationofatastesolutiontoonesideofthetonguewithapipette.
bElectrogustometer“HalleIV,”withstimulatingelectrode,tobeplacedupontongueorpalate.
cTastestrips withsweet,sour,salty,andbittertastesinfourconcentrationseach, tobeplacedupon thetongue's leftorrightside,with the
patientbeingrequiredtoindicatetheperceivedtasteinalist.
dExample ofgustatory-evokedpotentialsafter stimulationwith aceticacidvaporinapatientwithleft-sidedageusia: clearevokedpotential
afterstimulationoftherightside(bottomcurve,witharrowsindicatingpeaks)asopposedtotheleftside(topcurve,noevokedresponse).
LocalTasteTestsUsingAdequateStimuli
Adequatetastestimulimaybeappliedusingeitherliquidtastesolutionsorso-called tastestrips,
100–102
whichconsistofstripsoffilter paperimpregnatedwithtastesubstances. Liquidtastesolutionsmaybe
dabbedonwithcottonswabs,
103
orappliedbymeansofapipette
104
orsoakedpiecesoffilterpaper.
105
Usually, identificationthresholdsofeachgustatory areaareassessedusingincreasingconcentrationsof
tastesubstances.Patientsareinstructedtokeeptheir tongues immobile ina slightlyprotruded position
untiltheyhaveindicatedtheperceivedtastebypointingtotherespectivedescriptoronaboard;afterthat,
theyrinse their mouths with water. The tongue's extended positionduring testing is essential to avoid
distributionofthetastantoutsidethetestedregions;assoonasthetongueismovedintothemouth,tastants
willinevitablyspreadthroughouttheoralcavity,thwartinglocaltesting.
Advantagesofthetastestripsaretheirlongshelf-life,theoptionoflateralizedtesting,andavailability
ofseveralconcentrationsoftastants. Normativedatahavebeenestablished.
106
Theprocedureishighly
reliableandhasbeensuccessfullyusedinseveralclinicalstudies(e.g.,refs.107,108).
Inanothervarietyoftestsquantifyinggustation,intensityestimatesofdifferentconcentrationsoftaste
solutionsareobtainedeitherusingaratingscalerangingfrom“weak”throughto“strong”or,inacross-
modalapproach,bycomparisonwithvariablevolumesofa1,000-Hzsound.
103
Note

Whentastetestingtheanteriortwo-thirds ofthetongue,thetongue mustremainprotrudeduntil the
patienthasindicatedtheperceivedtastequality.
Electrogustometry
Electrogustometry, first introduced inthe 19thcentury, hasbeenestablishedas areliable procedure to
assessgustatoryfunction.
109
Perceptionthresholdsareobtainedbydirectcurrentstimulationwith1.5to
400µAinmonopolar(anodal)orbipolar(coaxial)mode.Itisimportanttocompareleft-andright-sided
function.
Electrogustometryissimpleandprovidesquickevidenceofnervelesions,buttherearealsoseveral
drawbacks: the method does not permit differentiation between taste qualities in gustatory disorders;
accompanying trigeminal sensations may occur at higher stimulus intensities; and correlation between
electricalandchemosensorytastetestingisweak.
110
Nevertheless,electrogustometrymayhaveaspecific
valueinseparatingageusiafromhypogeusia.
111
“Objective”Tests
Recordings of gustatory-evoked potentials are available in very few specialized centers (compare
olfactoryERP).Gustatorystimuliareappliedeithertothewholeoralcavityorinalateralizedfashion.
Atpresent,themethodisprimarilyusedinexperimentalandmedicolegalcontexts.
112
Occasionally,fMRIinresponsetogustatorystimulation(seeabove)maybeperformed,
73
butitsvalue
asadiagnostictoolinindividualcasesisyettobedemonstrated(Fig.6.5).
Note
Few centers offer “objective” techniques to assess taste disorders, such as gustatory ERPs or
gustatoryfMRI.
AssessmentofMorphologicalChanges
Two methods to assess morphological changes are available: biopsy (e.g., ref. 113) and contact
endoscopy(e.g.,ref.114).In thelatter,thetongue'sepitheliumisdyedwithmethyleneblueand a fiber
opticscopeisplacedonthemucosa,wherecellsarediscernibleat60to150×magnification.Thus,for
example,inpatientswithatransectedchordatympani,fewerandflatterfungiformpapillaearefoundin
theipsilateralepitheliumthan inthecontralateralepithelium
114
(Fig. 6.8). Inaddition,vascular meshes
beneath theepithelium are visible even without dye. Currently, however, this technique is not widely
available.
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Fig.6.8a–dContactendoscopy.(ImagescourtesyofTinoJust,Rostock.)(FromHummelT,Welge-LüssenA.Riech-undSchmeckstorungen:
Physiologie,PathophysiologieundTherapeutischeAnsatze.Stuttgart:Thieme;2005.)
aPartialdyingofthetonguepriortocontactendoscopy.
bArrowindicatesafungiformpapilla(fpap).
cArrowindicatesvasculararchitectureoffpap.
dSurfaceofanfpap(sameregion,dyedwithmethyleneblue);arrowindicatesporeofatastebud.
InvestigationoftheIntranasalTrigeminalSystem
Nostandardizedandclinicallyvalidatedpsychophysicaltestsareavailabletoassessthechemosensory
functionofthe trigeminalnerve.Inexperimentalcontexts,“lateralization”oftrigeminalstimuli
115–118
is
exploited:Unlikepureolfactorystimuli,nasalsensationssuchastingling,burning,stinging,ortickling—
elicitedinadditiontosmellsbymanyodorantsandmediatedbythetrigeminalnerve—maybelocalized.
Thus, after unilateral presentation of a bimodal olfactory/trigeminal stimulant such as menthol, the
stimulatednostrilcanbe identified,whereasthiswouldbeextremelydifficultwith a specificolfactory
stimulantsuchasvanillin.
115
Inaddition,thresholdassessmentoftrigeminalstimuli,andintensityestimatesin thesuprathreshold
range, may be performed.
119
Another, experimental, approach aims to record reflexive physiological
effects(e.g.,nasalsecretionorrespiration)inducedbytrigeminalstimulation(overviewinref.120).
“ChemosomatosensoryERP” is also usedtoassess the trigeminalsystem.
121,122
Typically, odorless
carbon dioxide is chosenas a stimulant which, at concentrationsabove 30%, and at200-millisecond
stimulusduration,elicitsburning, stingingsensations.Possibly, thesetrigeminalERPsmayalsoconvey

prognosticinformationconcerningsmelldisorders
66
(compareMinovietal2007
123
).Anothermethodof
investigatingthetrigeminalsystemistorecordpotentialsfromtherespiratorymucosa(negativemucosa
potential),
124
asophisticatedtechniquecurrentlyusedonlyinresearch(e.g.,refs.125–127).
Note
Few methods—and these mainly in experimental contexts—are available to assess trigeminal
chemosensoryfunction. However,itmay be assumedthatolfactorydisorders are accompaniedby
reduced trigeminal sensitivity
128
—an important aspect, particularly with respect to medicolegal
evidence(seeChapter18).
SummaryandOutlook
Tothoroughlyevaluatepatients’symptoms,detailed investigationofchemosensoryfunctionisrequired.
The availability of standardized procedures to assess smell and taste seems to be of the utmost
importanceinthedevelopmentofnewstrategiestocurechemosensorydysfunction.
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7SinonasalOlfactoryDisorders
MichaelDamm,RandyM.Leung,RobertC.Kern
Summary
Sinonasalolfactorydysfunctionhasahighprevalenceinthegeneralpopulation.Withintheotorhino
laryngological patient population, sinonasal diseases are responsible for about threequarters of
olfactorydysfunction.Theunderlyingcausesaremostfrequentlyinflammatorydiseasesofthenose
orthe paranasalsinuses(75%), whicharedefinedandcharacterizedinthissection.Itis assumed
thatmostsinonasal diseasesaffecttheolfactoryepitheliumsecondarily. Current informationabout
thepathophysiologyandtreatmentstrategiesofsinonasaldiseasesisincludedinthischapterbecause
improvementinolfactorydysfunctionisusuallyachievedbyimprovementoftheunderlyingdisease.
IntroductionandEpidemiolgy
Rhinitis and rhinosinusitis are broad terms that refer to conditions characterized by inflammation of
mucosaofthenoseand paranasal sinuses, typicallysubdividedonthe basis ofa temporal profile into
acute,recurrentacute,orchronicrhinosinusitis.
1–3
Itisnowwidelyacceptedthatincasesofrhinitis,the
paranasalsinusesarecommonlyaffectedaswell.
4
However,separatedefinitionsforthedifferententities
exist. Rhinitis is defined according to the consensus report of the International Rhinitis Management
WorkingGroup
5
as an inflammation ofthe liningofthe nose, andis characterized by nasal symptoms
including anterior or posterior rhinorrhea, sneezing, nasal blockage, or itching of the nose. These
symptomsoccurontwoormore consecutivedaysformore than1 hour onmostdays.
5
Considering the
etiology, we can distinguish between infectious and noninfectious, and between inflammatory and
noninflammatory, subtypes of rhinitis (Table 7.1).
6
Allergies and acute viral infections of the upper
respiratory tract are the most common causes of rhinitis. Viral rhinitis is the most prevalent disease
affectinghumans.
7
Allergicrhinitis(AR)isthemostcommonformofnoninfectiousrhinitis,thelifetime
prevalenceofARbeingabove20%.
8
Severalothernoninfectiousconditionscancausesimilarsymptoms:
hormonal imbalance, physical agents, anatomical anomalies, and the use of certain drugs.
6
Olfactory
impairment in rhinitis is usually reversible, but on many occasions the loss of olfaction persists.
9
Persistentpostviralorpostinfectiousolfactorydysfunctionhasbeenattributedinparticulartoinfluenza-
like infections.
10
If it follows one isolated acute infection of the upper respiratory tract, it should be
classed as postviral (postinfectious) olfactory dysfunction rather than rhinitis (see Chapter 8). Other
differentialdiagnosesofrhinitisarecondensedinTable7.2.
Acuterhinosinusitis(ARS)isdescribedasthepresenceofdrainageaccompaniedbynasalobstruction
or facial pain/pressure. ARS is most commonly preceded by a viral upper respiratorytract infection
(URTI);theUSadultpopulationsuffersfromanaverageof2.18URTIsperpersonperyear,ofwhichan
estimated0.5to2%developintoacutebacterialrhinosinusitis.
11,12
ThecriteriaforanARSepisodeshouldincludeatotaldurationofgreaterthan10days,soitcannotto
be confused with a viral respiratory infection, and less than 4 weeks to distinguish it from chronic
rhinosinusitis (CRS). Recurrent acute rhinosinusitis (RARS) is defined by four or more episodes of
bacterialARSperyearwithcompleteresolutionofsymptomsbetweenepisodes—althoughtheliterature
has diagnostic ranges fromtwo to fourper year.CRSis definedas morethan12 weeksofsymptoms
withoutaninterveningsymptom-freeperiod,
13
andisestimatedtoaffect13%oftheUSpopulation,or32
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