Dysosmia is a disorder described as any qualitative alteration or distortion of the perception of smell. Qualitative alterations differ from quantitative alterations, which include anosmia and hyposmia. Dysosmia can be classified as either parosmia (also called troposmia) or phantosmia. Parosmia refers to a distortion in the perception of an odorant. Odorants smell different from what one remembers. Phantosmia refers to the perception of an odor when there’s no actual odorant present. The etiology of dysosmia still remains a theory. It is typically considered a neurological disorder and clinical associations with the disorder have been made. Most cases are described as idiopathic and the main antecedents related to parosmia are URTIs, head trauma, and nasal and paranasal sinus disease. Dysosmia tends to go away on its own but there are options for treatment for patients that want immediate relief.
- 1 Olfactory system
- 2 Classification
- 3 Etiology
- 4 Diagnosis
- 5 Treatment
- 6 Occurrence
- 7 Impact
- 8 References
- 9 External links
Anatomy and Physiology
The olfactory neuroepithelium, located in the roof of the nasal chambers, comprises bipolar receptor cells, supporting cells, basal cells, and brush cells. There are approximately 6 million bipolar sensory receptor neurons whose cell bodies and dendrites are in the epithelium. The axons of these cells aggregate into 30-40 fascicles, called the olfactory fila, which project through the cribriform plate and pia matter. These axons collectively make up the olfactory nerve (CN I) and serve the purpose of mediating the sense of smell.
Characteristics of the bipolar receptor neurons include cilia on the dendritic ends which project into the mucus, regeneration from basal cells after damage, and each receptor neuron is also a first order neuron. The first order neurons project axons directly from the nasal chamber to the brain. Its first neuron characteristic allows direct exposure to the environment, which makes the brain vulnerable to infection and invasion of xenobiotic agents. Supporting cells, called sustentacular cells, provide metabolic and physical support to the receptors by insulating the cell and regulating the composition of the mucus. Basal stem cells give rise to both neurons and non-neuronal cells and allow for constant regeneration of receptor cells and its surrounding cell.
Olfactory transduction begins with the movement of odorants from the air phase to the aqueous phase in the olfactory mucus. Odorants are transported by odorant binding proteins or diffuse through the mucus and reach the cilia on the dendritic ends of bipolar receptor neurons. Stimulation causes action potentials to be initiated and the signals are sent to the brain via the olfactory fila.
Olfactory receptor neuron axons project through the cribriform plate to the olfactory bulb. The olfactory bulb is a structure at the base of the frontal lobe. It comprises neurons, nerve fibers, interneurons, microglia, astrocytes, and blood vessels. It is made up of 6 layers: olfactory nerve layer, glomerular layer, external plexiform layer, mitral cell layer, internal plexiform layer, and granule layer. The terminals of the receptor axons synapse with the dendrites of mitral and tufts cells within the glomeruli of the olfactory bulb. The axons of the mitral and tufts cells send signals to the olfactory cortex.
Signals from odor sensation are sent from the olfactory bulb through mitral and tufts cell axons via the lateral olfactory tract and synapse at the primary olfactory cortex. The primary olfactory cortex includes the anterior olfactory nucleus, the piriform cortex, the anterior cortical nucleus of the amygdala, the periamygdaloid complex, and the rostral entorhinal cortex. A unique characteristic of olfaction is its independence from the thalamus. The odor signals are sent directly from the sensory receptor neuron to the primary cortex. However, communication between the primary and secondary olfactory cortex requires connections with the thalamus.
Odor identity, quality, and familiarity are mainly deciphered by the piriform cortex. Consciousness of smell is achieved by projections from the piriform cortex to the medial dorsal nucleus of the thalamus and to the orbitofrontal cortex, which the secondary olfactory cortex is part of.
There are approximately 1000 olfactory receptors coded in the human genome. Less than 500 receptors are functional in the nasal epithelium. Each receptor neuron is a single type of olfactory receptor and is not specific to any one odorant. An odorant is recognized by more than one type of receptor and thus odorants are recognized by a combination of receptors. The olfactory system relies on different excitation patterns to obtain different codes for different odorants. Nobel prize recipient Linda B. Buck compared this system to combining different letters of the alphabet to produce different words. In this case, each word represents an odor. This coding explains why we can detect more odors than there are receptors in the nasal epithelium.
Olfaction and Flavor
Flavor is perceived by the combination of the sense of taste, sense of smell, and the trigeminal nerve (CN V). The gustatory system is responsible for differentiation between sweet, sour, salty, bitter, and umami. The olfactory system recognizes the odorants as they pass to the olfactory epithelium via a retronasal pathway. This explains why we can identify a variety of flavors in spite of only having five types of taste receptors. The trigeminal nerve senses texture, pain, and temperature of food. For example, the cooling effect of menthol or the burning sensation of spicy food.
Olfactory dysfunction can be quantitative and/or qualitative. Quantitative smell disorders refer to disorders in which there is complete or partial loss of olfaction. Anosmia, the complete loss of olfaction, and hyposmia, the partial loss of olfaction are the two disorders classified as quantitative because they can be measured. Qualitative smell disorders can’t be measured and refer to disorders in which there is alternation or distortion in the perception of smell. Qualitative disorders include parosmia (also called troposmia) and phantosmia. The term dysosmia refers to a qualitative olfaction disorder and include both parosmia and phantosmia. Olfactory dysfunction including anosmia, hyposmia, and dysosmia can be either bilateral or unilateral on either nostril. Anosmia only on the left nostril would be termed unilateral left anosmia while bilateral anosmia would be termed total anosmia.
Parosmia refers to a distortion in the perception of an odorant. Odorants smell different from what one remembers. A more specific term, cacosmia, refers to an unpleasant perception of an odorant due to nasosinusal or pharyngeal infection.
Phantosmia refers to the perception of an odor when there is no actual odorant present. When a phantom smell lasts less than a few seconds, the term olfactory hallucination can be used.
Even though the causes of dysosmia are not yet clear, there are two general theories that describe the etiology: the peripheral and central theories. In parosmia, the peripheral theory refers to the inability to form a complete picture of an odorant due to the loss of functioning olfactory receptor neurons. The central theory refers to integrative centers in the brain forming a distorted odor. In phantosmia, the peripheral theory refers to neurons emitting abnormal signals to the brain or the loss of inhibitory cells that are normally present in normal functioning. The central theory for phantosmia is described as an area of hyper-functioning brain cells that generate the order perception. Evidence to support these theories include findings that for the majority of individuals with distortions, there is a loss of sensitivity to smell that accompanies it and the distortions are worse at the time of the decreased sensitivity. It has been reported in parosmia cases that patients can identify triggering stimuli. Common triggers include gasoline, tobacco, coffee, perfum, fruits and chocolate.
- Upper respiratory tract infection (URTIs)
- Nasal and paranasal sinus disease
- Toxic chemical exposure
- Neurological abnormalities
- Head trauma
- Nasal surgery
- Tumors on the frontal lobe or olfactory bulb
Most of cases are described as idiopathic and the main antecedents related to parosmia are URTIs, head trauma, and nasal and paranasal sinus disease. Psychiatric causes for smell distortion can exist in schizophrenia, alcoholic psychosis, depression, and olfactory reference syndrome.
Diagnosing a patient can be difficult as they are often frustrated from ineffective therapy and being told they have mental illnesses. Some patients actually have trouble deciding whether they have a taste or smell problem. In this case asking questions about food choices will help determine whether a patient has a smell or taste disorder. It is important to identify whether the distortion applies to an inhaled odorant or if an odor exists without the stimulus. The distortion of an odorant is presented in two types: the stimuli are different from what one remembers and in the second, everything has a similar smell. A clinical history can also help determine what kind of disorder one has because events such as respiratory infection and head trauma are usually indications of parosmia where as phantosmias usually have no history of such events and occur spontaneously. Unfortunately there are no accurate diagnostic tests or methods for dysosmia. Evaluation must be done through questionnaires and medical history.
Even though dysosmia often goes away on its own over time, there are both medical and surgical treatments for dysosmia for patients that want immediate relief. Medical treatments include the use of topical nasal drops and oxymetazoline HCL, which give an upper nasal block so that the air flow can't reach the olfactory cleft. Other medications suggested include sedatives, anti-depressants, and anti- epileptic drugs. The medications may or may not work and for some patients, the side affects may not be tolerable. Most patients benefit from medical treatment but for some surgical treatment is required. Options include a bifrontal craniotomy and an excision of the olfactory epithelium, which cuts all of the fila olfactoria. According to some studies, transnasal endoscopic excision of the olfactory epithelium has been described as a safe and effective phantosmia treatment. The bifrontal craniotomy results in permanent anosmia and both surgeries are accompanied with the risks associated with general surgery.
The frequency of phantosmia is rare in comparison with the frequency of parosmia. Parosmia has been estimated to be in 10-60% of patients with olfactory dysfunction and from studies, it has been shown that it can last anywhere from 3 months to 22 years. Smell and taste problems result in over 200,000 visits to physicians annually in the US. Lately, it has been thought that phantosmia might co-occur with Parkinson’s disease. However, its potential to be a premotor biomaker for Parkinson’s is still up for debate as not all patients with Parkinson’s disease have olfactory disorders
Smell disorders can result in the inability to detect environmental dangers such as gas leaks, toxins, or smoke. In addition to safety, nutritional and eating habits can also be affected. There is a loss of appetite because of unpleasant flavor and fear of failing to recognize and consuming spoiled food. A decreased or distorted sense of smell therefore results in a decreased quality of life. Distortions are believed to have a greater negative impact on people than the complete loss of smell because they are constantly reminded of the disorder and the distortions have a greater effect on eating habits.
- Leopold, D (2002). "Distortion of olfactory perception: Diagnosis and treatment". Chemical Senses 27 (7): 611–5. doi:10.1093/chemse/27.7.611. PMID 12200340.
- Frasnelli, J (2004). "Clinical presentation of qualitative olfactory dysfunction". Eur Arch Otorhinolaryngol 261: 411–415. doi:10.1007/s00405-003-0703-y. PMID 14610680.
- Doty, R (2009). "The olfactory system and its disorders". Seminars in Neurology 29 (1): 74–81. doi:10.1055/s-0028-1124025. PMID 19214935.
- Bonfils, P; Avan, P; Patrick Faulcon; David Malinvaud (2005). "Distorted odorant perception analysis of a series of 56 patients with parosmia". Arch Otolayngol Head Neck Surg 131: 107–112. doi:10.1001/archotol.131.2.107. PMID 15723940.
- Kalogjera, L; Dzepina, D (2012). "Management of smell dysfunction". Curr Allergy Asthma Rep 12: 154–62. doi:10.1007/s11882-012-0248-5. PMID 22297924.
- Doty, R (2001). "Olfaction". Annu. Rev. Psychol 52: 423–452. doi:10.1146/annurev.psych.52.1.423.
- Hummel, T; Landis, B; Huttenbrink, K-B (2011). "Smell and taste disorders". GMS Current Topics in Otorhinolaryngology Head and Neck Surgery 10: 1865-1011. doi:10.3205/cto000077. PMID 22558054.
- Nordin, S; Murphy, C; Davidson, T; Quinonez, C et al. (1996). "Prevalence and assessment of qualitative olfactory dysfunction in different age groups". Laryngoscope 106 (6): 739–44. doi:10.1097/00005537-199606000-00014. PMID 8656960.
- Leopold, D; Loehrl, T; Schwob, J (2002). "Long-term follow up of surgically treated phantosmia". Arch Otolayngol Head Neck Surg 128 (6): 642–647. doi:10.1001/archotol.128.6.642. PMID 12049557.
- Landis, B; Burkhard, P (2008). "Phantosmias and Parkinson Disease". Arch Neurol 65 (9): 1237–9. doi:10.1001/archneur.65.9.1237. PMID 18779429.