Semin Plast Surg 2012; 26(02): 076-082
DOI: 10.1055/s-0032-1320065
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Pierre Robin Sequence

Noopur Gangopadhyay
1   Plastic and Reconstructive Surgery, Washington University School of Medicine, Saint Louis, Missouri
,
Derick A. Mendonca
1   Plastic and Reconstructive Surgery, Washington University School of Medicine, Saint Louis, Missouri
,
Albert S. Woo
1   Plastic and Reconstructive Surgery, Washington University School of Medicine, Saint Louis, Missouri
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Publikationsverlauf

Publikationsdatum:
12. Juli 2012 (online)

Abstract

Pierre Robin sequence (PRS) is classically described as a triad of micrognathia, glossoptosis, and airway obstruction. Infants frequently present at birth with a hypoplastic mandible and difficulty breathing. The smaller mandible displaces the tongue posteriorly, resulting in obstruction of the airway. Typically, a wide U-shaped cleft palate is also associated with this phenomenon. PRS is not a syndrome in itself, but rather a sequence of disorders, with one abnormality resulting in the next. However, it is related to several other craniofacial anomalies and may appear in conjunction with a syndromic diagnosis, such as velocardiofacial and Stickler syndromes.

Infants with PRS should be evaluated by a multidisciplinary team to assess the anatomic findings, delineate the source of airway obstruction, and address airway and feeding issues. Positioning will resolve the airway obstruction in ~70% of cases. In the correct position, most children will also be able to feed normally. If the infant continues to show evidence of desaturation, then placement of a nasopharyngeal tube is indicated. Early feeding via a nasogastric tube may also reduce the amount of energy needed and allow for early weight gain. A proportion of PRS infants do not respond to conservative measures and will require further intervention. Prior to considering any surgical procedure, the clinician should first rule out any sources of obstruction below the base of the tongue that would necessitate a tracheostomy. The two most common procedures for treatment, tongue–lip adhesion and distraction osteogenesis of the mandible, are discussed.

 
  • References

  • 1 Sommerlad B. Cleft palate. In: Guyuron B, Eriksson E, Persing J, eds. Plastic Surgery Indications and Practice. Philadelphia, PA: Saunders Elsevier; 2009: 508-509
  • 2 Mackay DR. Controversies in the diagnosis and management of the Robin sequence. J Craniofac Surg 2011; 22 (2) 415-420
  • 3 Hunt JA, Hobar PC. Common craniofacial anomalies: the facial dysostoses. Plast Reconstr Surg 2002; 110 (7) 1714-1725 , quiz 1726, discussion 1727–1728
  • 4 Izumi K, Konczal LL, Mitchell AL , et al. Underlying genetic diagnosis of Pierre Robin sequence: retrospective chart review at two children's hospitals and a systematic literature review. J Pediatr 2012; 160 (4) 645-650 , e2
  • 5 Jakobsen LP, Knudsen MA, Lespinasse J , et al. The genetic basis of the Pierre Robin sequence. Cleft Palate Craniofac J 2006; 43 (2) 155-159
  • 6 Jakobsen LP, Ullmann R, Christensen SB , et al. Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2. J Med Genet 2007; 44 (6) 381-386
  • 7 Shprintzen RJ. The implications of the diagnosis of Robin sequence. Cleft Palate Craniofac J 1992; 29 (3) 205-209
  • 8 Marcellus L. The infant with Pierre Robin sequence: review and implications for nursing practice. J Pediatr Nurs 2001; 16 (1) 23-34
  • 9 Marques IL, Monteiro LC, de Souza L, Bettiol H, Sassaki CH, de Assumpção Costa R. Gastroesophageal reflux in severe cases of Robin sequence treated with nasopharyngeal intubation. Cleft Palate Craniofac J 2009; 46 (4) 448-453
  • 10 Gosain AK, Nacamuli R. Embryology of the head and neck. In: Thorne CH, Beasley RW, Aston SJ, et al, eds. Grabb & Smith's Plastic Surgery. 6th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 1997: 179-190
  • 11 Cheng AT, Corke M, Loughran-Fowlds A, Birman C, Hayward P, Waters KA. Distraction osteogenesis and glossopexy for Robin sequence with airway obstruction. ANZ J Surg 2011; 81 (5) 320-325
  • 12 Cruz MJ, Kerschner JE, Beste DJ, Conley SF. Pierre Robin sequences: secondary respiratory difficulties and intrinsic feeding abnormalities. Laryngoscope 1999; 109 (10) 1632-1636
  • 13 Chang AB, Masters IB, Williams GR, Harris M, O'Neil MC. A modified nasopharyngeal tube to relieve high upper airway obstruction. Pediatr Pulmonol 2000; 29 (4) 299-306
  • 14 Anderson KD, Cole A, Chuo CB, Slator R. Home management of upper airway obstruction in Pierre Robin sequence using a nasopharyngeal airway. Cleft Palate Craniofac J 2007; 44 (3) 269-273
  • 15 Al-Samkari HT, Kane AA, Molter DW, Vachharajani A. Neonatal outcomes of Pierre Robin sequence: an institutional experience. Clin Pediatr (Phila) 2010; 49 (12) 1117-1122
  • 16 Wagener S, Rayatt SS, Tatman AJ, Gornall P, Slator R. Management of infants with Pierre Robin sequence. Cleft Palate Craniofac J 2003; 40 (2) 180-185
  • 17 Skillman J, Cole A, Slator R. Sodium supplementation in neonates with Pierre Robin sequence significantly improves weight gain if urinary sodium is low. Cleft Palate Craniofac J 2012; 49 (1) 39-43
  • 18 Rogers GF, Murthy AS, LaBrie RA, Mulliken JB. The GILLS score: part I. Patient selection for tongue-lip adhesion in Robin sequence. Plast Reconstr Surg 2011; 128 (1) 243-251
  • 19 Bartlett SP, Losee JE, Baker SB. Reconstruction: craniofacial syndromes. In: Mathes SJ, ed. Plastic Surgery. Vol. 4. Philadelphia, PA: Saunders Elsevier; 2006: 514-516
  • 20 Bijnen CL, Don Griot PJW, Mulder WJ, Haumann TJ, Van Hagen AJ. Tongue-lip adhesion in the treatment of Pierre Robin sequence. J Craniofac Surg 2009; 20 (2) 315-320
  • 21 Kirschner RE, Low DW, Randall P , et al. Surgical airway management in Pierre Robin sequence: is there a role for tongue-lip adhesion?. Cleft Palate Craniofac J 2003; 40 (1) 13-18
  • 22 Sedaghat AR, Anderson IC, McGinley BM, Rossberg MI, Redett RJ, Ishman SL. Characterization of obstructive sleep apnea before and after tongue-lip adhesion in children with micrognathia. Cleft Palate Craniofac J 2012; 49 (1) 21-26
  • 23 Denny AD, Amm CA, Schaefer RB. Outcomes of tongue-lip adhesion for neonatal respiratory distress caused by Pierre Robin sequence. J Craniofac Surg 2004; 15 (5) 819-823
  • 24 Boston M, Rutter MJ. Current airway management in craniofacial anomalies. Curr Opin Otolaryngol Head Neck Surg 2003; 11 (6) 428-432
  • 25 Fritz MA, Sidman JD. Distraction osteogenesis of the mandible. Curr Opin Otolaryngol Head Neck Surg 2004; 12 (6) 513-518
  • 26 Kobayashi A, Yoshimasu H, Kobayashi J, Amagasa T. Neurosensory alteration in the lower lip and chin area after orthognathic surgery: bilateral sagittal split osteotomy versus inverted L ramus osteotomy. J Oral Maxillofac Surg 2006; 64 (5) 778-784
  • 27 Denny A, Amm C. New technique for airway correction in neonates with severe Pierre Robin sequence. J Pediatr 2005; 147 (1) 97-101
  • 28 Molina F, Ortiz Monasterio F. Mandibular elongation and remodeling by distraction: a farewell to major osteotomies. Plast Reconstr Surg 1995; 96 (4) 825-840 , discussion 841–842
  • 29 McCarthy JG, Schreiber J, Karp N, Thorne CH, Grayson BH. Lengthening the human mandible by gradual distraction. Plast Reconstr Surg 1992; 89 (1) 1-8 , discussion 9–10
  • 30 Monasterio FO, Molina F, Berlanga F , et al. Swallowing disorders in Pierre Robin sequence: its correction by distraction. J Craniofac Surg 2004; 15 (6) 934-941