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Causes of Persistent Obstructive Sleep Apnea Despite Previous Tonsillectomy and Adenoidectomy in Children with Down Syndrome as Depicted on Static and Dynamic Cine MRI

Lane F. Donnelly1,2, Sally R. Shott3, Connor R. LaRose1, Barbara A. Chini2,4 and Raouf S. Amin2,4

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



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Fig. 1A. Recurrent enlargement of adenoid tonsils in 10-year-old girl with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. A = adenoid tissue. Sagittal T1-weighted image shows recurrent and enlarged adenoid tissue narrowing posterior nasopharynx (arrow). Macroglossia is also present.

 


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Fig. 1B. Recurrent enlargement of adenoid tonsils in 10-year-old girl with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. A = adenoid tissue. Sagittal fast spin-echo inversion recovery image shows recurrent and enlarged adenoid tissue as increased signal, narrowing posterior nasopharynx (arrow).

 


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Fig. 1C. Recurrent enlargement of adenoid tonsils in 10-year-old girl with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. A = adenoid tissue. Axial fast spin-echo inversion recovery image shows recurrent and enlarged adenoid tissue as increased signal, narrowing posterior nasopharynx (arrow).

 


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Fig. 1D. Recurrent enlargement of adenoid tonsils in 10-year-old girl with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. A = adenoid tissue. Consecutive images from sagittal cine MRI sequence show enlarged adenoid tissue. Posterior nasopharynx (large arrow) and hypopharynx (small arrows, E) are well-defined and show low signal in D and are poorly defined and show high signal in E. Cine display of images showed intermittent collapse of nasopharynx and hypopharynx.

 


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Fig. 1E. Recurrent enlargement of adenoid tonsils in 10-year-old girl with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. A = adenoid tissue. Consecutive images from sagittal cine MRI sequence show enlarged adenoid tissue. Posterior nasopharynx (large arrow) and hypopharynx (small arrows, E) are well-defined and show low signal in D and are poorly defined and show high signal in E. Cine display of images showed intermittent collapse of nasopharynx and hypopharynx.

 


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Fig. 2A. Recurrent enlargement of adenoid tonsils in 7-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from cine MRI sequence show enlarged adenoid tissue (A on A). In A, nasopharynx (small arrow) and hypopharynx (large arrows) are patent. In B, nasopharynx (small arrows) and hypopharynx (large arrows) have decreased in caliber and are nearly collapsed. Cine display of images showed intermittent collapse of nasopharynx and hypopharynx.

 


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Fig. 2B. Recurrent enlargement of adenoid tonsils in 7-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from cine MRI sequence show enlarged adenoid tissue (A on A). In A, nasopharynx (small arrow) and hypopharynx (large arrows) are patent. In B, nasopharynx (small arrows) and hypopharynx (large arrows) have decreased in caliber and are nearly collapsed. Cine display of images showed intermittent collapse of nasopharynx and hypopharynx.

 


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Fig. 3A. Enlarged lingual tonsils obstructing hypopharynx in 10-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Axial (A) and sagittal (B) fast spin-echo inversion recovery images show high-signal lingual tonsil (L) at level of base of tongue, filling and obstructing hypopharynx. Recurrence of adenoid tissue (A) is also seen in B.

 


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Fig. 3B. Enlarged lingual tonsils obstructing hypopharynx in 10-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Axial (A) and sagittal (B) fast spin-echo inversion recovery images show high-signal lingual tonsil (L) at level of base of tongue, filling and obstructing hypopharynx. Recurrence of adenoid tissue (A) is also seen in B.

 


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Fig. 3C. Enlarged lingual tonsils obstructing hypopharynx in 10-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from cine MRI sequence show that lingual tonsils are not seen in region of hypopharynx (C). In D, lingual tonsils (L) are seen filling and obstructing hypopharynx. Cine display of images showed intermittent inferior and central motion of lingual tonsils intermittently obstructing hypopharynx.

 


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Fig. 3D. Enlarged lingual tonsils obstructing hypopharynx in 10-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from cine MRI sequence show that lingual tonsils are not seen in region of hypopharynx (C). In D, lingual tonsils (L) are seen filling and obstructing hypopharynx. Cine display of images showed intermittent inferior and central motion of lingual tonsils intermittently obstructing hypopharynx.

 


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Fig. 4A. Glossoptosis with associated lack of median sulcus and fatty infiltration of tongue musculature in 12-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Midline sagittal T1-weighted spin-echo image shows macroglossia with encroachment on small-caliber hypopharynx (large arrow). Increased signal (small arrow) is present in musculature of tongue, consistent with fatty infiltration.

 


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Fig. 4B. Glossoptosis with associated lack of median sulcus and fatty infiltration of tongue musculature in 12-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from axial cine MRI sequence show that hypopharynx (arrow, C) is decreased on both images. Interval decrease in diameter occurs from B to C. Cine display of images showed intermittent posterior motion of tongue, consistent with glossoptosis and resulting in intermittent obstruction of hypopharynx.

 


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Fig. 4C. Glossoptosis with associated lack of median sulcus and fatty infiltration of tongue musculature in 12-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from axial cine MRI sequence show that hypopharynx (arrow, C) is decreased on both images. Interval decrease in diameter occurs from B to C. Cine display of images showed intermittent posterior motion of tongue, consistent with glossoptosis and resulting in intermittent obstruction of hypopharynx.

 


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Fig. 4D. Glossoptosis with associated lack of median sulcus and fatty infiltration of tongue musculature in 12-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Axial fast spin-echo inversion recovery image shows lack of normal median sulcus and small-caliber hypopharynx (arrow).

 


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Fig. 4E. Glossoptosis with associated lack of median sulcus and fatty infiltration of tongue musculature in 12-year-old boy with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. For comparison purposes, axial fast spin-echo inversion recovery image of 12-year-old boy with obstructive sleep apnea but not Down syndrome shows normal appearance of median sulcus (arrow) of tongue.

 


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Fig. 5A. Macroglossia and glossoptosis in 18-year-old woman with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from sagittal cine MRI sequence show macroglossia with posterior aspect of tongue (arrows) encroaching on hypopharynx. Interval decrease in caliber of hypopharynx with associated obstruction occurs from A to B. Cine display of images showed intermittent posterior motion of tongue, consistent with glossoptosis and resulting in intermittent obstruction of hypopharynx.

 


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Fig. 5B. Macroglossia and glossoptosis in 18-year-old woman with Down syndrome and persistent obstructive sleep apnea despite previous tonsillectomy and adenoidectomy. Consecutive images from sagittal cine MRI sequence show macroglossia with posterior aspect of tongue (arrows) encroaching on hypopharynx. Interval decrease in caliber of hypopharynx with associated obstruction occurs from A to B. Cine display of images showed intermittent posterior motion of tongue, consistent with glossoptosis and resulting in intermittent obstruction of hypopharynx.

 

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