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CONGENITAL LARYNGEAL DISORDERS DR PRASHANTH
CLASSIFICATION 1. SUPRAGLOTTIS LARYNGOMALACIA         LARYNGEAL CYST CONGENITAL LARYNGOCELE     2. GLOTTIS LARYNGEAL WEB          CRI-DU CHAT SYNDROME          VOCAL CORD PARALYSIS
CLASSSIFICATION CONTD…. 3. SUBGLOTTIS:         SUBGLOTTIC STENOSIS         SUBGLOTTIC HEMANGIOMA         LARYNGOTRACHEAL CLEFT
LARYNGOMALACIA MALACIA= SOFTENING (GREEK) JACKSON IN 1942 MOST  COMMON  CAUSE  OF  CONGENITAL   STRIDOR. FEATURES:       1. SOFT FLABBY LARYNGEAL TISSUES       2. THIN LARYNGEAL CARTILAGES       3. LOOSE, REDUNDANT MUCOSA OF            LARYNX
C/F:        M:F= 1:1,   CRY IS NORMAL        INSPIRATORY STRIDOR:  HIGH PITCH,        “FLUTTERING” , WITHIN FEW DAYS OF        BIRTH , OR URTI INCREASES TILL         FIRST YEAR STARTS RESOLVING.         SUPINE POSITION, SUCKLING, CRYING        WORSENS STRIDOR        IMPROVES IN PRONE POSITION
DIAGNOSIS:       HISTORY       VIDEOLARYNGOSCOPY/FLEXIBLE  NASO        LARYNGOSCOPY:             1. OMEGA SHAPED EPIGLOTTIS             2. SHORT AE FOLD, PROLAPSES                    INWARDS             3. PROMINENT ARYTENOIDS, LOOSE                 MUCOSA, MOVE INWARDS             4. DIFFICULT TO SEE VOCAL CORDS
TREATMENT:       1.  90% CASES RESOLVE BY 2  YEARS        2.  TREAT  URTI EFFECTIVELY        SEVERE RESPIRATORY DISTRESS,         FEEDING DIFFICULTY( HIGH  INTRA        THORACIC NEGATIVE PRESSURE        GERD )  WITH FAILURE TO THRIVE                 ACTIVE    INTERVENTION
            EMERGENCY MANAGEMENT:           1. ENDOTRACHEAL  INTUBATION           2. TEMPORARY TRACHEOSTOMY
         CONSERVATIVE MANAGEMENT    ENDOSCOPIC  ARY- EPIGLOTTOPLASTY                ( SUPRAGLOTTOPLASTY) CO2 / COLD KNIFE    AE FOLD RELEASED FROM  EPIGLOTTIS  &  REDUNDANT MUCOSA OF ARYTENOID EXCISED IF NEEDED ALONG WITH CUNEIFORM CARTILAGES
 LARYNGOCELE AIR-FILLED DILATATION OF SACCULUS ETIOLOGY:    1. CONGENITALLY LARGE SACCULE    2. INCREASED INTRA LARYNGEAL         PRESSURE  GAS BLOWERS,          SAXOPHONE PLAYERS, COUGHING etc
TYPES: Internal-  within the larynx External- Projects through the thyro-hyoid  membrane and presents as swelling in the lateral neck Combined
CLINICAL FEATURES Asymptomatic Hoarseness RESPIRATORY DISTRESS INCREASES ON CRYING OR STRAINING Neck: Cystic, painless swelling, reducible, increases on valsalva ILS: Smooth bulge on the ventricular band, may obscure the vocal cords
BRYCE’S SIGN:          GIRGLING  &  HISSING  SOUND IN          THROAT WHEN EXTERNAL MASS          IS COMPRESSED     IF SAC OPENING IS OBSTRUCTED     MUCOCELE ( SACCULAR CYST )
MANAGEMENT SOFT TISSUE XRAY NECK/ CT SCAN DURING VALSALVA DIRECT LARYNGOSCOPY TO RULE OUT UNDERLYING MALIGNANCY TREATMENT: MLS & MARSUPIALIZATION  OF SAC (VENTRICULAR BAND & LARYNGOCELE IS CUT & MARGINS EVERTED) EXTERNAL (TRANSCERVICAL) EXCISION      (EITHER CUT THE NECK OF SAC & SUTURE        OR LARYNGOFISSURE & SAC EXCISION)
LARYNGEAL WEB FAILURE OF COMPLETE CANALIZATION OF LARYNX DURING 5TH WEEK OF IU LIFE MOST COMMON IS GLOTTIC WEB(75%), LESS COMMON ARE SUPRA & SUB GLOTTIC  MOSTLY ANTERIOR GLOTTIC WEBS  POSTERIOR INTERARYTENOID WEBS MAY BE ASSOCIATED WITH CRICOARYTENOID JOINT FIXATION
C/F:   WEAK CRY AT BIRTH   RECURRENT CROUP   INSPIRATORY OR BIPHASIC STRIDOR DIAGNOSIS:       VIDEODIRECT ENDOSCOPY/ FLEXIBLE        NASOLARYNGOSCOPY
Rx:   ASYMPTOMATIC   REASSURANCE
PREFERABLY KEEL INSERTED AT AGE OF 3 YRS & ABOVE TEMPORARY TRACHEOSTOMY  WHEN KEEL IN-SITU ( 2- 5 WEEKS) INSERTED ENDOSCOPICALLY WITH COMBINEDLARYNGOFISSURE APPROACH VERY SEVERE WEB INVOLVING SUBGLOTTIS  EMERGENCY TRACHEOSTOMY AT 2 yrsLTR ( Laryngo tracheal reconstruction)     WITH   ANTERIOR CARTILAGE GRAFTING
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Congenital laryngeal disorders

  • 2. CLASSIFICATION 1. SUPRAGLOTTIS LARYNGOMALACIA LARYNGEAL CYST CONGENITAL LARYNGOCELE 2. GLOTTIS LARYNGEAL WEB CRI-DU CHAT SYNDROME VOCAL CORD PARALYSIS
  • 3. CLASSSIFICATION CONTD…. 3. SUBGLOTTIS: SUBGLOTTIC STENOSIS SUBGLOTTIC HEMANGIOMA LARYNGOTRACHEAL CLEFT
  • 4. LARYNGOMALACIA MALACIA= SOFTENING (GREEK) JACKSON IN 1942 MOST COMMON CAUSE OF CONGENITAL STRIDOR. FEATURES: 1. SOFT FLABBY LARYNGEAL TISSUES 2. THIN LARYNGEAL CARTILAGES 3. LOOSE, REDUNDANT MUCOSA OF LARYNX
  • 5. C/F: M:F= 1:1, CRY IS NORMAL INSPIRATORY STRIDOR: HIGH PITCH, “FLUTTERING” , WITHIN FEW DAYS OF BIRTH , OR URTI INCREASES TILL FIRST YEAR STARTS RESOLVING. SUPINE POSITION, SUCKLING, CRYING WORSENS STRIDOR IMPROVES IN PRONE POSITION
  • 6. DIAGNOSIS: HISTORY VIDEOLARYNGOSCOPY/FLEXIBLE NASO LARYNGOSCOPY: 1. OMEGA SHAPED EPIGLOTTIS 2. SHORT AE FOLD, PROLAPSES INWARDS 3. PROMINENT ARYTENOIDS, LOOSE MUCOSA, MOVE INWARDS 4. DIFFICULT TO SEE VOCAL CORDS
  • 7.
  • 8.
  • 9. TREATMENT: 1. 90% CASES RESOLVE BY 2 YEARS 2. TREAT URTI EFFECTIVELY SEVERE RESPIRATORY DISTRESS, FEEDING DIFFICULTY( HIGH INTRA THORACIC NEGATIVE PRESSURE GERD ) WITH FAILURE TO THRIVE ACTIVE INTERVENTION
  • 10. EMERGENCY MANAGEMENT: 1. ENDOTRACHEAL INTUBATION 2. TEMPORARY TRACHEOSTOMY
  • 11. CONSERVATIVE MANAGEMENT ENDOSCOPIC ARY- EPIGLOTTOPLASTY ( SUPRAGLOTTOPLASTY) CO2 / COLD KNIFE  AE FOLD RELEASED FROM EPIGLOTTIS & REDUNDANT MUCOSA OF ARYTENOID EXCISED IF NEEDED ALONG WITH CUNEIFORM CARTILAGES
  • 12. LARYNGOCELE AIR-FILLED DILATATION OF SACCULUS ETIOLOGY: 1. CONGENITALLY LARGE SACCULE 2. INCREASED INTRA LARYNGEAL PRESSURE  GAS BLOWERS, SAXOPHONE PLAYERS, COUGHING etc
  • 13.
  • 14. TYPES: Internal- within the larynx External- Projects through the thyro-hyoid membrane and presents as swelling in the lateral neck Combined
  • 15.
  • 16. CLINICAL FEATURES Asymptomatic Hoarseness RESPIRATORY DISTRESS INCREASES ON CRYING OR STRAINING Neck: Cystic, painless swelling, reducible, increases on valsalva ILS: Smooth bulge on the ventricular band, may obscure the vocal cords
  • 17. BRYCE’S SIGN: GIRGLING & HISSING SOUND IN THROAT WHEN EXTERNAL MASS IS COMPRESSED IF SAC OPENING IS OBSTRUCTED  MUCOCELE ( SACCULAR CYST )
  • 18. MANAGEMENT SOFT TISSUE XRAY NECK/ CT SCAN DURING VALSALVA DIRECT LARYNGOSCOPY TO RULE OUT UNDERLYING MALIGNANCY TREATMENT: MLS & MARSUPIALIZATION OF SAC (VENTRICULAR BAND & LARYNGOCELE IS CUT & MARGINS EVERTED) EXTERNAL (TRANSCERVICAL) EXCISION (EITHER CUT THE NECK OF SAC & SUTURE OR LARYNGOFISSURE & SAC EXCISION)
  • 19. LARYNGEAL WEB FAILURE OF COMPLETE CANALIZATION OF LARYNX DURING 5TH WEEK OF IU LIFE MOST COMMON IS GLOTTIC WEB(75%), LESS COMMON ARE SUPRA & SUB GLOTTIC MOSTLY ANTERIOR GLOTTIC WEBS POSTERIOR INTERARYTENOID WEBS MAY BE ASSOCIATED WITH CRICOARYTENOID JOINT FIXATION
  • 20. C/F: WEAK CRY AT BIRTH RECURRENT CROUP INSPIRATORY OR BIPHASIC STRIDOR DIAGNOSIS: VIDEODIRECT ENDOSCOPY/ FLEXIBLE NASOLARYNGOSCOPY
  • 21.
  • 22. Rx: ASYMPTOMATIC  REASSURANCE
  • 23.
  • 24.
  • 25.
  • 26. PREFERABLY KEEL INSERTED AT AGE OF 3 YRS & ABOVE TEMPORARY TRACHEOSTOMY WHEN KEEL IN-SITU ( 2- 5 WEEKS) INSERTED ENDOSCOPICALLY WITH COMBINEDLARYNGOFISSURE APPROACH VERY SEVERE WEB INVOLVING SUBGLOTTIS  EMERGENCY TRACHEOSTOMY AT 2 yrsLTR ( Laryngo tracheal reconstruction) WITH ANTERIOR CARTILAGE GRAFTING