Zusammenfassung
Die juvenile Larynxpapillomatose ist eine seltene, durch humane Papillomaviren (HPV)
verursachte Erkrankung. Bei aggressiven Verlaufsformen sind bleibende Stimm- und Atemstörungen
durch eine Vielzahl notwendiger Papillomabtragungen bisher kaum zu vermeiden. Um die
Rezidivrate bei schwerer Verlaufsform zu senken, werden heute die Immunstimulation
mit Interferon alpha oder die lokale Applikation von Cidofovir empfohlen. Auch Mumps-Impfungen
und eine fotodynamische Therapie werden angewendet. Im vorliegenden Fall wurde versucht,
durch Immunisierung mit dem quadrivalenten HPV-Spaltimpfstoff Gardasil® den Krankheitsverlauf
bei einem zweijährigen Jungen, der seit 9 Monaten erkrankt war, positiv zu beeinflussen.
Durch chromogene In-situ-Hybridisierung und Polymerase-Kettenreaktion (PCR) an Läsionsgewebe
war eine simultane HPV-Infektion durch HPV-Typ 6 und 11 nachgewiesen. Nach der dritten
Impfung stabilisierte sich der Krankheitsverlauf. In den bisher zehn Monaten nach
der letzten Impfung war kein erneuter Progress erkennbar. Aufgrund des geringen Risikos
dieser Form der adjuvanten Behandlung halten wir eine multizentrische Studie zur Klärung
der Wirksamkeit für gerechtfertigt, auch wenn eine vollständige Viruselimination mit
diesem Impfstoff nicht wahrscheinlich ist.
Juvenile Laryngeal Papillomatosis – Immunisation with the Polyvalent Vaccine Gardasil®
Juvenile laryngeal papillomatosis is a rare condition caused by human papilloma virus
(HPV). In cases with rapid recurrences permanent impairments of voice and breathing
are almost inevitable due to the frequent need of debulking surgeries. Efforts to
lower the recurrence rate comprise the adjuvant use of interferon alpha, local cidofovir,
photodynamic therapy or mumps vaccination.
In the present case we tried to positively influence the aggressive course of disease
in a two year old boy by immunisation with the quadrivalent HPV vaccine Gardasil®.
Chromogenic in-situ hybridisation analysis and polymerase chain reaction (PCR) of
lesion tissue showed simultaneous infection with the HPV-Types 6 and 11. After the
third immunisation the disease became stable. No further surgery was necessary for
the last ten months.
The risk profile of this adjuvant treatment is low. We think it worth to initiate
a multicentre trial to prove a benefit of this treatment even if no complete virus
elimination can be achieved.
Schlüsselwörter
Larynx - HPV - Papillomavirus - Gardasil - Larynxpapillomatose - Fallbericht
Key words
larynx - papillomavirus - HPV - Gardasil - laryngeal papillomatosis - case report
Literatur
- 1
Derkay C S.
Task force on recurrent respiratory papillomas. A preliminary report.
Arch Otolaryngol Head Neck Surg.
1995;
121
1386-1391
- 2
Alberico S, Pinzano R, Comar M. et al .
Maternal-fetal transmission of human papillomavirus.
Minerva Ginecol.
1996;
48
199-204
- 3
Terry R M, Lewis F A, Griffiths S, Wells M, Bird C C.
Demonstration of human papillomavirus types 6 and 11 in juvenile laryngeal papillomatosis
by in-situ DNA hybridization.
J Pathol.
1987;
153
245-248
- 4
Mounts P, Shah K V, Kashima H.
Viral etiology of juvenile- and adult-onset squamous papilloma of the larynx.
Proc Natl Acad Sci USA.
1982;
79
5425-5429
- 5
Reeves W C, Ruparelia S S, Swanson K I. et al .
National registry for juvenile-onset recurrent respiratory papillomatosis.
Arch Otolaryngol Head Neck Surg.
2003;
129
976-982
- 6
Ruparelia S, Unger E R, Nisenbaum R, Derkay C S, Reeves W C.
Predictors of remission in juvenile-onset recurrent respiratory papillomatosis.
Arch Otolaryngol Head Neck Surg.
2003;
129
1275-1278
- 7
Kimberlin D W.
Current status of antiviral therapy for juvenile-onset recurrent respiratory papillomatosis.
Antiviral Res.
2004;
63
141-151
- 8
Gerein V, Rastorguev E, Gerein J, Draf W, Schirren J.
Incidence, age at onset, and potential reasons of malignant transformation in recurrent
respiratory papillomatosis patients: 20 years experience.
Otolaryngol Head Neck Surg.
2005;
132
392-394
- 9
Aaltonen L M, Rihkanen H, Vaheri A.
Human papillomavirus in larynx.
Laryngoscope.
2002;
112
700-707
- 10
Stamataki S, Nikolopoulos T P, Korres S. et al .
Juvenile recurrent respiratory papillomatosis: still a mystery disease with difficult
management.
Head Neck.
2007;
29
155-162
- 11
Gerein V, Rastorguev E, Gerein J, Jecker P, Pfister H.
Use of interferon-alpha in recurrent respiratory papillomatosis: 20-year follow-up.
Ann Otol Rhinol Laryngol.
2005;
114
463-471
- 12
Pudszuhn A, Welzel C, Bloching M, Neumann K.
Intralesional Cidofovir application in recurrent laryngeal papillomatosis.
Eur Arch Otorhinolaryngol.
2007;
264
63-70
- 13
Neumann K, Pudszuhn A, Welzel C, Bartel-Friedrich S, Passmann M.
Intralesional cidofovir injections for recurrent laryngeal papillomatosis: first results.
Laryngo-Rhino-Otol.
2003;
82
700-706
- 14
Shikowitz M J, Abramson A L, Steinberg B M. et al .
Clinical trial of photodynamic therapy with meso-tetra (hydroxyphenyl) chlorin for
respiratory papillomatosis.
Arch Otolaryngol Head Neck Surg.
2005;
131
99-105
- 15
Pashley N R.
Can mumps vaccine induce remission in recurrent respiratory papilloma?.
Arch Otolaryngol Head Neck Surg.
2002;
128
783-786
- 16
Villa L L, Costa R L, Petta C A. et al .
High sustained efficacy of a prophylactic quadrivalent human papillomavirus types
6/11/16/18 L1 virus-like particle vaccine through 5 years of follow-up.
Br J Cancer.
2006;
95
1459-1466
- 17
Glastetter E, Kaufmann A M.
Humoral and cellular immune response in HPV vaccination.
Hautarzt.
2007;
58
493-500
- 18
Garland S M, Hernandez-Avila M, Wheeler C M. et al .
Quadrivalent vaccine against human papillomavirus to prevent anogenital diseases.
N Engl J Med.
2007;
356
1928-1943
- 19
Maloney E M, Unger E R, Tucker R A. et al .
Longitudinal measures of human papillomavirus 6 and 11 viral loads and antibody response
in children with recurrent respiratory papillomatosis.
Arch Otolaryngol Head Neck Surg.
2006;
132
711-715
- 20
Chen B B, Zhao K N, Liu X S. et al .
The detection and significance of human papilloma virus 11b virus like particles and
its serum antibody in juvenile larynx papilloma.
Zhonghua Er Bi Yan Hou Ke Za Zhi.
2003;
38
417-420
- 21
Roda Husman A-M, Walboomers J MM, Brule A JC, Meijer C JLM, Snijders P JF.
The use of geneal primers PG5 and PG6 elongated at their 3' ends with adjacent highly
conserved sequences improves human papillomavirus detection by PCR.
J Gen Virol.
1995;
76
1057-1062
- 22
Hallez S, Simon P, Maudoux F. et al .
Phase I/II trial of immunogenicity of a human papillomavirus (HPV) type 16 E7 protein-based
vaccine in women with oncogenic HPV-positive cervical intraepithelial neoplasia.
Cancer Immunol Immunother.
2004;
53
642-650
- 23
Waterboer T, Sehr P, Michael K M. et al .
Multiplex Human Papillomavirus Serology Based on in Situ-Purified Glutathione S-Transferase
Fusion Proteins.
Clin Chem.
2005;
51
1845-1853
Dr. med. Gerhard Förster
Klinik für HNO-Heilkunde/Plastische Operationen
SRH Wald-Klinikum Gera
Straße des Friedens 122
07548 Gera
Email: gerhard.foerster@wkg.srh.de