ENT and mucopolysaccharidoses

Ear, nose, and throat (ENT) manifestations in mucopolysaccharidosis (MPS) are due to the accumulation of glycosaminoglycans (GAGs) in the head and neck region. The ENT manifestations are very common and include protruding or depressed frontal bone, a depressed nasal bridge, wide nasal alae, thick lips, angled and hypoplastic mandible (micrognathia), macroglossia, distorted teeth, gingival hypertrophy, and also restriction of the mouth opening, adenotonsillary hypertrophy, and thickening of soft tissues in the laryngopharynx. Head and neck disorders affect more than 90% of MPS patients [1, 2]. The median age of a first ENT visit is 4.2 years, generally prior to MPS diagnosis [3‐9]. Symptoms such as “noisy breathing”, sleep apnoea, frequent respiratory and ear infections, chronic nasal discharge, and enlargement of the tongue, tonsils, and adenoids may often predate a definitive MPS diagnosis by several years, particularly in patients with an attenuated phenotype. MPS, owing to the non-specific nature of the early symptoms, is therefore often unrecognized [10, 11]. The early recognition and prompt diagnosis of MPS disorders is crucial. Early treatment considerably improves patient outcomes during long-term therapy and is crucial to slow disease progression before irreversible damage occurs. Undiagnosed patients are frequently referred to otolaryngologists for ENT manifestations; these specialists thus have an early opportunity to recognize MPS. Therefore, the otolaryngologist is an essential member of the care management team for the disorders of MPS patients and they are in a prime position to initiate diagnostic work-up and referral for definitive testing [9].

ENT disease in MPS can be schematically divided into respiratory disorders and otological or hearing problems.

In summary, otolaryngologists often see as yet undiagnosed MPS patients. Their careful history collection and clinical evaluation may play an important role in the diagnosis and management plan.

Respiratory disorders occur in all type of MPS. Airway problems result from a combination of tissue storage of GAGs that produce a distortion of airway anatomy and function [10, 12‐16]. Affected individuals classically have a number of anatomical features predisposing to airway dysfunction [17]. Progressive airway damage develops, often involving multiple levels within the upper respiratory tract, secondary to the progressive deposition of GAGs within the airway [18], at any level from the “lips to lungs” [19]. Airway problems include obstructive sleep apnoea (OSA), frequent respiratory infections, adenoid (Fig. 1) and tonsillar hypertrophy (Fig. 2), irregular nasal septum, turbinate hypertrophy, macroglossia (Fig. 3), thickened pharyngeal wall, laryngeal abnormalities, tracheomalacia, tracheal stenosis and short neck, dyspnoea, restricted joint mobility, skeletal abnormalities, and increased mucus secretions in the upper and lower airways [20‐24]. Chronic rhinosinusitis and chronic otitis media may occur and produce hearing impairment [10, 12]. In extreme cases, excessive tissue on the arytenoid cartilages and aryepiglottic folds can prolapse into the laryngeal inlet causing stridor and airway obstruction [24]. Furthermore, hepatosplenomegaly may limit diaphragmatic excursion, and interstitial pulmonary GAG deposits may result in a diffusion defect [13]. Thickened and copious secretions throughout the upper and lower respiratory tracts are also commonly found and there is a tendency for frequent upper and lower respiratory tract infections. Recurrent throat and ear infections are present in more than 50% of patients [25]. However, due to the low number of patients, no conclusions can be made regarding the prevalence and severity of respiratory problems for each MPS type [18]. Initially, obstructive symptoms are more pronounced in the upper airway; tracheobronchial manifestations occur later. The respiratory involvement is usually progressive and can result in morbidity and mortality early in childhood [10, 26].

The respiratory disorders in MPS can be divided into airway abnormalities (extrathoracic and intrathoracic), and alterations in respiratory and sleeping mechanics [18].

Extrathoracic anatomical abnormalities, including abnormal cervical vertebrae, a short neck, a relatively high epiglottis, deep cranial fossa narrowing the nasopharynx, a hypoplastic mandible with a short ramus, temporomandibular joint ankylosis, a small thoracic cage, frequently complicated by kyphoscoliosis [13, 27, 28], and mucopolysaccharide infiltration of the nasopharyngeal, oropharyngeal, hypopharyngeal, and laryngeal tissues, are typically seen in children with MPS and predispose them to upper airway obstruction [29]. Intrathoracic airway obstruction is also a common complication, and tracheobronchial abnormalities due to enlarged cartilage cells or soft-tissue growths can also cause narrowing of the tracheal lumen [18]. The trachea can be narrow, tortuous, or occluded by the accumulation of soft tissue [29]. Semenza et al. [17] also suggested alveolar and interstitial pulmonary involvement by GAG deposition. Depending on the site and severity of obstruction, patients may present with stridor, dyspnoea, retractions, cough, cyanosis, or difficulty with feeding [26], and the severity of respiratory dysfunction varies according to the MPS type [29].

Multiple abnormalities in MPS patients can reduce the ventilator capacity, manifesting as a reduction in vital capacity [18]. Short stature [30], kyphoscoliosis, and pectus carinatum are common, and diaphragm excursion may be compromised by hepatosplenomegaly [13, 30]. Tracheal distortion is characteristic for MPS and may reflect a disproportionate length of the trachea relative to the shortened spinal length [31, 32]. In combination with laxity of the tracheal tissue, it can cause airway collapse [31]. Cervical or lumbar spinal cord lesions may weaken expiratory muscles, impair cough, and reduce secretion clearance, predisposing patients to recurrent pneumonia. Diaphragmatic weakness may result from spinal cord compression above the phrenic nerve origin [18]. The combined effect of these alterations in respiratory mechanics together with airway abnormalities may lead to respiratory failure. Airway obstruction and parenchymal abnormality can impair pulmonary O₂ uptake and CO₂ excretion [18]. Ventilatory dysfunction is exacerbated by normal sleep mechanisms that increase upper airway collapsibility [33]. The severity of respiratory damage varies according to the MPS type [3, 9, 17, 29, 34‐38] (Table 1). The prevalence of obstructive sleep apnoea syndrome (OSAS) is between 100% of cases as reported by Lin et al. [14] and 33% of MPS patients as described by Kiely et al. [3]. The prevalence of OSAS in patients with MPS was reported as 69.8% by Moreira et al. [39]. Upper airway obstruction has been described for all MPS disorders [40] (Table 2). Other studies in the literature report intermediate percentages [1‐3, 12‐15, 41‐43] (Table 3). MPS I and MPS VI patients appear to be at the greatest risk for severe OSA [1, 15, 42].

Currently, treatment of airway obstruction in patients with MPS is controversial, and has met with only moderate success [29]. Management of airway involvement begins with the surgical removal of the obstruction [37], and the accumulation of GAGs in the adenoids and tonsils, with resulting hypertrophy, makes these structures frequent targets for surgical intervention [2]. Therefore, MPS patients with clinical symptoms of upper airway obstruction are often subjected to adenoidectomy and/or tonsillectomy, with data reported in the literature ranging from 70 to 20% of cases [1‐3, 7, 12, 19, 29, 34, 37, 42] (Table 4). Tonsil volume increase is also secondary to GAG deposits in the tonsillar fossa. In principle, this would make coblation intracapsular tonsillectomy not recommendable for treatment of OSA in MPS children [38]. Adenoidectomy and/or tonsillectomy in 35–50% of cases are performed prior to MPS diagnosis [7, 44]. Despite adenotonsillectomy being a routine procedure in most children, the risks are usually higher in an MPS child, including post-operative haemorrhage, airway oedema, and failure to extubate [10]. Therapeutically, adenoidectomy and tonsillectomy provide initial but only temporary relief of upper airway obstruction. Furthermore, the recurrence rate of adenoid hypertrophy after adenoidectomy in the MPS population is 56% [1, 45], while in the normal population it is between 0.55 and 1.5% [42]. Adenotonsillectomy alone may not be a sufficient treatment for upper airway obstruction in patients with MPS. The limited relief afforded by adenotonsillectomy is attributable to the multifactorial pathogenesis of airway obstruction and the benefit of the procedure also depends on the extent and severity of airway narrowing at other levels [10].

When local airway procedures are no longer adequate, or when there is significant tracheobronchial involvement, non-invasive continuous positive airway pressure (CPAP) may be employed by some patients during sleep [19] and it is often added to the management plan [37]. It may provide temporary relief for some of these patients before surgical intervention, but it is generally poorly tolerated in patients with behavioural disturbance [10] and may become less effective as the airway disease progresses [29]. If patients tolerate CPAP but hypoxaemia persists, bi-level positive airway pressure (BiPAP) can be advantageous in patients with additional respiratory failure and baseline low oxygen levels.

Progression of upper airway obstruction when less invasive interventions are no longer adequate may often require a tracheotomy. Tracheotomy in MPS children may be performed to treat refractory progressive upper airway obstruction, to safeguard an anticipated difficult airway management before a planned non-ENT surgical procedure, and in emergency airway management. Yeung et al. report a rate of 11% for tracheotomy [29]. This rate compares with those in other studies reported in the literature [2, 7, 12, 19, 29, 37, 38, 46] (Table 5). Computed tomographic scan of the chest and airway is recommended prior to surgery to exclude airway narrowing distally from the carina [26] and multidetector computed tomography (MDCT) is suggested for pre-operative airway assessment [47]. MDCT images produce additional information on the glottic and subglottic structures, and airway reconstruction using MDCT derived from previous CT studies could provide a useful assessment tool in the pre-operative airway evaluation and planning of anaesthesia for MPS children. All tracheotomies in patients with MPS result in tracheotomy-related complications. Infrastomal tracheal stenosis is the most frequent complication (85.7%), and stomal narrowing (Fig. 4) also occurs frequently (71.4%) after each tracheotomy [46]. Granulation formation and wound infection are described [18]. These complications cause difficult cannula care, with a high frequency of surgery revisions. Airway problems may persist after tracheotomy due to persistent airway collapse distal to the tip of the endotracheal tube [21], and tracheobronchial stents may be useful [48, 49].

Hearing loss is almost a universal finding in children with MPS [29, 50, 51]. From the hearing standpoint, it is very common to find conductive hearing loss. However, many patients present a sensorineural component [52]. The conductive component of hearing loss is attributed to the presence of seromucinous otitis (Fig. 5) or bone chain deformities [53], disruption in ossicular conduction by histopathological anomalies similar to otosclerosis, or by arthropathy [54]. Sensorineural hearing loss (SHL) is thought to be caused by the accumulation of GAGs in the cochlea, auditory nerve, and brain stem. Auditory pathophysiology in the central nervous system in Hurler syndrome remains unknown [55]; however, decreased cochlear hair cells may be one of the important factors for the sensorineural component of hearing loss. In many patients, mixed-type hearing loss can also be seen. In MPS II (Hunter syndrome), the most prevalent otolaryngological manifestations and interventions reported are otitis (either acute otitis media or chronic otitis media [72%]), hearing loss (67%), insertion of ventilation tubes (50%), adenoidectomy (47%), and hearing aids (41%) [5]. Tables 6 and 7 describe the different audiological findings in subtypes of MPS [52, 56].

Early recognition of MPS requires careful attention to the presence of multiple signs and symptoms, many of which overlap with common childhood complaints. Children with MPS have a high risk of hearing loss and this is an early symptom. Thus, early otolaryngological evaluation and intervention are recommended [56]. Clinical suspicion of the disease can be triggered by particular clusters of signs and symptoms that are unlikely to appear in an unaffected child but that often occur together in the child with MPS II (Table 8).

Sensorineural or mixed conductive and sensorineural hearing loss commonly develop in Morquio A patients in the first decade of life [57]. Conductive hearing loss due to retained middle ear fluid can be treated using ventilation tubes. Long-lasting types of tympanostomy tubes (Fig. 6) are preferable for use on the first occasion considering the anaesthetic risks and the risk of the re-occurrence of the middle ear fluid. Post-aural hearing aids may be most appropriate if a progressive neurosensory element to hearing loss is present. However, despite hearing normalisation after placement of transtympanic drainage tubes, this does not exempt such patients from a periodic audiological follow-up [51, 58]. Both amplification with hearing aids and transtympanic ventilation tubes appear to be effective in improving language development in children with moderate cognitive impairment [59]. Periodic follow-up of these patients is mandatory because of hearing impairment and consequences for their development and quality of life.