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DOI:10.2214/AJR.07.3020
AJR 2008; 190:973-975
© American Roentgen Ray Society


Original Research

The Frequency of Lingual Tonsil Enlargement in Obese Children

Carolina V. A. Guimaraes1, Maninder Kalra2, Lane F. Donnelly1,2, Sally R. Shott3, Kelly Fitz2, Saroj Singla2 and Raouf S. Amin2

1 Department of Radiology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave., MLC 5031, Cincinnati, OH 45229-3039.
2 Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
3 Division of Otolaryngology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

Received August 13, 2007; accepted after revision October 17, 2007.

 
Address correspondence to L. F. Donnelly (Lane.Donnelly{at}cchmc.org).


Abstract
Top
Abstract
Introduction
Subjects and Methods
Results
discussion
References
 
OBJECTIVE. Enlargement of the lingual tonsils is being increasingly recognized as a not uncommon and treatable cause of obstructive sleep apnea, particularly in patients with Down syndrome who have undergone palatine tonsillectomy and adenoidectomy. We have recognized an increasing number of patients who are obese and have obstructive sleep apnea with enlarged lingual tonsils. The purpose of this study was to evaluate the frequency of enlarged lingual tonsils in obese children.

SUBJECTS AND METHODS. Seventy-one obese children (mean body mass index = 41.6 kg/m2) underwent sagittal fast spin-echo inversion recovery imaging. Lingual tonsils were identified and measured in the greatest anteroposterior diameter. Lingual tonsils > 10 mm were considered markedly enlarged. The subgroup with absent palatine tonsils (previous tonsillectomy) (n = 41) were compared with those with palatine tonsils present (n = 30).

RESULTS. Forty-four (62%) of the obese children had measurable lingual tonsils, which is greater than the frequency previously reported in normal subjects (0%), subjects with obstructive sleep apnea (33%), or subjects with Down syndrome and obstructive sleep apnea (50%). Ten (14%) had lingual tonsils > 10 mm. Obese subjects with absent palatine tonsils (previous tonsillectomy) had a higher prevalence of measurable lingual tonsils than those with palatine tonsils (78% vs 22%, respectively; p < 0.001) and a higher prevalence of lingual tonsils > 10 mm (90% vs 10%, p < 0.001).

CONCLUSION. Obese children have a high frequency of enlargement of the lingual tonsils with a significantly higher prevalence in those with previous tonsillectomy. Enlarged lingual tonsils may play a role in the pathogenesis of obstructive sleep apnea in obese children.

Keywords: adenoidectomy • childhood obesity • lingual tonsils • obstructive sleep apnea • pediatric imaging • tonsillectomy


Introduction
Top
Abstract
Introduction
Subjects and Methods
Results
discussion
References
 
Obstructive sleep apnea is increasingly being recognized as a significant cause of morbidity in children [14]. It is estimated that approximately 3% of all children have obstructive sleep apnea [1]. In particular, obese children are at increased risk of obstructive sleep apnea, with up to 55% of obese adolescents having obstructive sleep apnea [5].

Enlargement of the lingual tonsils is increasingly being recognized as a cause of obstructive sleep apnea [14] and has been identified as a significant cause of obstructive sleep apnea, particularly in children with Down syndrome who have undergone palatine tonsillectomy and adenoidectomy. In this patient population, it is a cause of persistent sleep apnea in 35% [2]. It is important to identify enlargement of the lingual tonsils as a cause of obstructive sleep apnea because it is one of the surgically curable causes of obstructive sleep apnea [4]. We have subjectively recognized an increased incidence of lingual tonsillar enlargement in obese children. The purpose of this study was to evaluate the frequency of enlarged lingual tonsils in obese children.


Subjects and Methods
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Abstract
Introduction
Subjects and Methods
Results
discussion
References
 
The study was reviewed and approved by our institutional review board. Informed consent was obtained. Data were stored in a secured and HIPAA-compliant fashion. Lingual tonsils were evaluated on MRI in 71 obese children.

Subjects
Children were recruited for MRI as part of a research protocol. Subjects were recruited from obese children seeking treatment at our institution's sleep center. Children were imaged while well and without upper respiratory illness.

The inclusion criteria were as follows: age of > 13 and < 21 years at evaluation visit and obesity, defined as body mass index (BMI) > 95th percentile for age and sex. The exclusion criteria were a craniofacial deformity, ongoing orthodontic problems requiring braces, pregnancy, weight > 375 lb (169 kg) or BMI > 55 kg/m2.

MRI Sequence
The size of the lingual tonsils was measured on fast spin-echo (FSE) inversion recovery (IR) images. All imaging studies were obtained on a 1.5-T unit (Signa Excite HD, GE Healthcare) with subjects positioned supine within a head and neck vascular coil. The technical parameters for the sagittal FSE IR images included a TR/TE, 5,000/34; echo-train length, 12; field of view, 22 cm; slice thickness, 6 mm; gap, 2 mm; matrix, 256 x 192; and 2 signal acquisitions.

Lingual Tonsil Diameter
The maximum transverse diameter of the lingual tonsil was measured perpendicular to the long axis of the lingual tonsil in an oblique anterior-to-posterior plane. Measurements were made by a fellow in pediatric radiology after training with a pediatric radiology faculty member (13 years' experience). All measurements were reviewed by the fellow and faculty member simultaneously and any issues were resolved by consensus. The lingual tonsils were categorized as nonvisualized, present and measurable, or markedly enlarged. Markedly enlarged was defined as a transverse diameter of greater than 10 mm. "Nonvisualized" was defined as no bright-signal tonsillar tissue was present in the expected location of the lingual tonsils.

Previous Palatine Tonsillectomy and Adenoidectomy
The subjects were divided into those who had undergone tonsillectomy and adenoidectomy with absent palatine tonsils and V-shaped surgical defect in the adenoid tonsils on MRI and those who had not. There were 41 subjects in the previous tonsillectomy and adenoidectomy group and 30 patients with no previous tonsillectomy and adenoidectomy. Statistical evaluation was performed to determine whether there was a difference in the frequency of lingual tonsils being present (chi-square test) or markedly enlarged (Fisher's exact test) between the two groups. A p value of less than 0.05 was considered statistically significant.


Figure 1
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Fig. 1 Nonvisualized lingual tonsils in 12-year-9 month-old girl. Sagittal fast spin-echo inversion recovery image shows no bright signal in expected location of lingual tonsils (arrow).

 

Results
Top
Abstract
Introduction
Subjects and Methods
Results
discussion
References
 
The study population was composed of 71 subjects (36 girls, 35 boys) with a mean age (± SD) of 15.67 ± 2.3 years. Forty-four (62%) of the 71 obese children had visualized and measurable lingual tonsils. Ten (14%) had markedly enlarged lingual tonsils. The mean diameter of the lingual tonsils was 5.16 mm with a range of 0.0 to 15.2 mm. The MR appearances of the lingual tonsils are shown in Figures 1, 2, 3.


Figure 2
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Fig. 2 Visualized and measurable lingual tonsils in 17-year-9 month-old girl. Sagittal fast spin-echo inversion recovery image shows measurable lingual tonsils (arrow), which measure 5 mm.

 

Figure 3
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Fig. 3 Markedly enlarged lingual tonsils in 16-year-old boy. Sagittal fast spin-echo inversion recovery image shows markedly enlarged lingual tonsils (arrows), which measure 15 mm.

 
Results for the comparison between the frequency of lingual tonsils in patients with and without previous tonsillectomy and adenoidectomy are summarized in Table 1. The frequency of the lingual tonsils being present and the frequency of the lingual tonsils being markedly enlarged were greater in the group with previous tonsillectomy and adenoidectomy than in the group who had not undergone tonsillectomy and adenoidectomy.


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TABLE 1: Lingual Parameters of Obese Subjects Who Had Undergone Previous Palatine Tonsillectomy and Adenoidectomy Compared with Those Who Had Not

 


discussion
Top
Abstract
Introduction
Subjects and Methods
Results
discussion
References
 
Over the past several decades, there has been a marked interval increase in the prevalence of obesity in pediatric patients [58]. Pediatric obesity is now recognized as being of epidemic proportions. The condition causes the greatest morbidity and mortality during adulthood of any current pediatric illness.

One of the complications of pediatric obesity is obstructive sleep apnea. It is well recognized that obese subjects are at increased risk for obstructive sleep apnea. One study found that 55% of obese adolescents had significant obstructive sleep apnea [5]. Furthermore, it has been shown that with increasing BMI there is a trend for ever higher prevalence of obstructive sleep apnea.

Although the relationship between obesity and obstructive sleep apnea is well established, the exact cause of obstructive sleep apnea in obese subjects is debated [5, 9, 10]. There are multiple potential contributing factors to the cause of obstructive sleep apnea in obese subjects. These include increased parapharyngeal fat impinging on the airway, increased prevalence of tonsillar tissue, increased elasticity of the walls of the airway related to decreased muscular tone, and poorly understood central effects related to things such as increased visceral adiposity [5, 9, 10].

Obstructive sleep apnea can occur from anatomic obstruction of the supraglottic airway, increased collapsibility of the airway, or some combination of the two [1]. One of the more common anatomic levels of obstruction is at the retroglossal airway [1]. Because of the anatomic position of the lingual tonsils in this region, enlargement of the lingual tonsils can contribute to significant obstructive sleep apnea [14]. It is important to recognize this potential cause of obstructive sleep apnea because it is easily rectified by surgical resection [4]. We have seen multiple cases in which significant obstructive sleep apnea has resolved after lingual tonsillectomy in a patient with enlarged lingual tonsils.

In this study, we found a high frequency of both measurable and markedly increased size of lingual tonsils in obese subjects. The frequency of lingual tonsils in obese subjects is greater than that previously seen in the normal population and in patients with Down syndrome and obstructive sleep apnea [2, 3]. The frequency of measurable lingual tonsils on MRI reported in the literature in asymptomatic children without obstructive sleep apnea is 0%, in children with obstructive sleep apnea in general is 33%, and in patients with Down syndrome and obstructive sleep apnea is 50% [3]. It is important to recognize that the increased size of the lingual tonsils may be one of many contributing factors to the development of obstructive sleep apnea in obese subjects. Further investigations into whether there is significant correlation between the presence of lingual tonsils and obstructive sleep apnea may be warranted.

Studies have shown that in patients with Down syndrome, previous palatine tonsillectomy and adenoidectomy are associated with an increased risk of overgrowth of the lingual tonsils [2]. Interestingly, in our study, there was a statistically significant increased rate of presence and marked enlargement of lingual tonsils in the children who had undergone palatine tonsillectomy and adenoidectomy. These findings suggest that in obese patients, previous palatine tonsillectomy and adenoidectomy are risk factors for enlargement of the lingual tonsils.

In summary, obese children have an increased incidence of both the presence and marked enlargement of the lingual tonsils. Enlargement of the lingual tonsils may be one of the contributing factors to the development of obstructive sleep apnea in obese subjects. This is particularly true in obese children who have previously undergone palatine tonsillectomy and adenoidectomy.


References
Top
Abstract
Introduction
Subjects and Methods
Results
discussion
References
 

  1. Donnelly LF. Obstructive sleep apnea in pediatric patients: evaluation with cine MR sleep studies. Radiology2005; 236:768 -778[Abstract/Free Full Text]
  2. Donnelly LF, Shott SR, LaRose CR, Chini BA, Amin RS. Causes of persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy in children with Down syndrome as depicted on static and dynamic cine MRI. AJR 2004;183 : 175-181[Abstract/Free Full Text]
  3. Fricke BL, Donnelly LF, Shott SR, et al. Comparison of lingual tonsil size as depicted on MR imaging between children with obstructive sleep apnea despite previous tonsillectomy and adenoidectomy and normal controls. Pediatr Radiol 2006;36 : 518-523[CrossRef][Medline]
  4. Shott SR, Donnelly LF. Cine magnetic resonance imaging: evaluation of persistent airway obstruction after tonsil and adenoidectomy in children with Down syndrome. Laryngoscope 2004;114 : 1724-1729[CrossRef][Medline]
  5. Kalra M, Inge T, Garcia V, et al. Obstructive sleep apnea in extremely overweight adolescents undergoing bariatric surgery. Obesity Res 2005;13 : 1175-1179[Medline]
  6. Kimm SY, Barton BA, Obarzanek E, et al.; NHLBI Growth and Health Study. Obesity development during adolescence in a biracial cohort: the NHLBI Growth and Health Study. Pediatrics 2002;110 : e54[Abstract/Free Full Text]
  7. Strauss RS, Pollack HA. Epidemic increase in childhood overweight, 1986–1998. JAMA 2001;286 : 2845-2848[Abstract/Free Full Text]
  8. Styne DM. Childhood and adolescent obesity: prevalence and significance. Pediatr Clin North Am 2001;48 : 823-854[CrossRef][Medline]
  9. Kalra M, Chakraborty R. Genetic susceptibility to obstructive sleep apnea in the obese child. Sleep Med 2007;8 : 169-175[CrossRef][Medline]
  10. Okubo M, Suzuki M, Horiuchi A, et al. Morphologic analyses of mandible and upper airway soft tissue by MRI of patients with obstructive sleep apnea hypopnea syndrome. Sleep2006; 29:909 -915[Medline]

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This Article
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