Dokument: Vulvakarzinom im Wandel der Zeit
Titel: | Vulvakarzinom im Wandel der Zeit | |||||||
Weiterer Titel: | Vulvar squamous cell carinoma - changes in time | |||||||
URL für Lesezeichen: | https://docserv.uni-duesseldorf.de/servlets/DocumentServlet?id=54667 | |||||||
URN (NBN): | urn:nbn:de:hbz:061-20201111-110854-5 | |||||||
Kollektion: | Dissertationen | |||||||
Sprache: | Deutsch | |||||||
Dokumententyp: | Wissenschaftliche Abschlussarbeiten » Dissertation | |||||||
Medientyp: | Text | |||||||
Autor: | Heinevetter, Kim Viviane [Autor] | |||||||
Dateien: |
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Beitragende: | Prof. Dr. Hampl, Monika [Gutachter] PD Dr. med. Reifenberger, Julia [Gutachter] | |||||||
Stichwörter: | Vulvakarzinom, vulvar squamous cell carcinoma, Vulva Ca | |||||||
Dewey Dezimal-Klassifikation: | 600 Technik, Medizin, angewandte Wissenschaften » 610 Medizin und Gesundheit | |||||||
Beschreibungen: | Zusammenfassung
Einleitung: Die Inzidenz des Vulvakarzinoms ist steigend, wobei der größte Anstieg bei Frauen im 50.-60.LJ zu verzeichnen ist und mit einer Abnahme des mittleren Erkrankungsalters einhergeht. Plattenepithelkarzinome der Vulva (VSCC) treten am häufigsten in der vorderen Kommissur der Vulva auf. Man differenziert in HPV-abhängige und -unabhängige Formen. HPV-abhängige VSCC entstehen eher bei jüngeren Frauen, verhornen nicht und gehen mit einer besseren Prognose einher. Lokoregionale operative Therapiemethoden sind weniger radikal geworden, während sich bei deutlich verbesserter Lebensqualität statistisch kaum erhöhte Rezidivraten zeigen. Zielsetzung: Ziel dieser Studie war es im Zeitintervall 2004-2014 Veränderungen hinsichtlich Inzidenz, Epidemiologie, Alter, Diagnostik, Therapie sowie postoperativer Komplikationen des VSCC in der UFK in Düsseldorf zu analysieren. Material und Methoden: In dieser klinisch-retrospektiven Studie wurden bei 314 Patientinnen mit VSCC der UFK Düsseldorf mittels Aktenrecherche oben genannte Parameter erhoben. Zwei Zeitintervalle, 2004-2009 und 2010-2014, wurden miteinander statistisch mit χ²- und T-Test in Bezug auf (signifikante) Unterschiede verglichen. Ergebnisse: Es zeigte sich ein Anstieg der Fallzahlen um das 2,5-fache zwischen 2004-2014, wobei das Alter bei Ersterkrankung stabil war. Im Vergleich zu den Altersangaben des RKI (72 Jahre mittleres Erkrankungsalter) waren unsere Frauen deutlich jünger (58 Jahre). 99% der Karzinome waren VSCC, davon 85% keratinisierend und 14% nicht-verhornend. In klinisch HPV-verdächtigen VSCC konnte in 95% der Fälle HPV-DNA nachgewiesen werden. Es zeigte sich eine Erhöhung der mittleren Infiltrationstiefe um 2 mm, während die häufigste Lokalisation mit 73% die vordere Kommissur darstellt. Die Lokalexzision des Tumors hat die radikale Vulvektomie (VE) als zweithäufigste Operationstechnik nach der partiellen VE abgelöst. Sentinel- Lymphonodektomien (SNLE) wurden 40% häufiger durchgeführt, wohingegen die inguinofemoralen Lymphknotendissektionen (IFLND) um 56% zurückgingen. Postoperative Beschwerden nahmen um 20% ab. Diskussion Insgesamt zeigen sich steigende Fallzahlen des VSCC. Die im klinischen Alltag beobachtete Zunahme an jungen Frauen mit Vulvakarzinom hat sich mit dem Alter bei Erstdiagnose im gesamten Beobachtungszeitraum in unserem Zentrum bestätigt. Ob der Inzidenzanstieg durch einen Anstieg HPVabhängiger VSCC bedingt ist, lässt sich aus unseren retrospektiven Daten nicht eruieren und kann nur über eine Testung auf HPV-DNA und Surrogat-Marker im Tumor erhoben werden. Dies könnte zu einer gezielten Therapieplanung auch bei dieser Tumorentität (targeted therapy) beitragen. Zukünftig ist ein Abfall der HPV-Inzidenz durch die Vakzinierung zu erwarten. Weniger radikale Operationsverfahren gehen mit unveränderter Rezidivrate und einer besseren Lebensqualität einher und sollten weiter vermehrt eingesetzt werden.Abstract Introduction: The incidence of vulvar squamous cell carcinoma increased during the last decades, especially in women aged 50-60, while the age of disease onset decreased. The area between urethra and clitoris is the most common localisation of VSCC. There are HPV associated and HPV independent forms of vulvar cancer. HPV associated VSCC are most likely diagnosed in younger women. They do not keratinize and go along with a better prognosis. Local operation techniques have become less radical while recurrence rates barely changed. Aim: Changes concerning incidence, age of onset, diagnostics, therapy and complications during the years 2004-2014 in patients treated at the Department of Gynecology and Obstetrics of the University Hospital of Düsseldorf were evaluated. Methods: This is a retrospective clinical study including data of patients treated with VSCC at the University Hospital of Düsseldorf during 2004-2014. Patients have been divided in two time periods, 2004-2009 and 2010-2014, regarding year of diagnosis. Both groups were analysed and compared with statistic tests (χ²- und T-Test) to evaluate possible significant effects. Results: The number of VSCC rose about 2.5 times during the time period 2004-2014. Age of onset did not change. In comparison to mean age of onset of VSCC in Germany (mean age 72) our patients were younger (mean age 58). 99% of all the cases of vulvar cancer were VSCC while 85% of them were keratinized tumors. When HPV-associated VSCC was clinically suspected, HPV-DNA was detected in 95% of the cases. Mean tumor infiltration increased by 2mm in average. The most common localisation was the area between clitoris and urethra (72%). Local resection of the tumor is now the second most common type of surgery performed instead of total vulvectomy. The most common type of operation performed is partial vulvectomy. While use of sentinel node biopsies increased about 40% the number of performed total inguinal lymphonodectomies decreased about 56%. Percentage of surgical complications decreased by 20%. Discussion: Overall there is an increase of VSCC. The increase of younger women diagnosed with VSCC - as observed in clinical practice - has been verified by our data. Retrospectively it is not possible to differentiate if the rise of incidence is caused by HPV-associated VSCC or not. To find an answer, all VSCC have to be tested for HPV-DNA and surrogate markers. In the future this could also lead to a more specific cancer therapy (targeted therapy). Due to HPV-vaccination a decrease of vaccine type HPV-incidence is likely. Less radical operation techniques have no influence on the recurrence rate but at the same time improve quality of life of the women and therefore should continue to be used more frequently. | |||||||
Quelle: | ABBAS, S. & SEITZ, M. 2011. Systematic review and meta-analysis of the used
surgical techniques to reduce leg lymphedema following radical inguinal nodes dissection. Surg Oncol, 20, 88-96. ACHIMAS-CADARIU, P., HARTER, P., FISSELER-ECKHOFF, A., BEUTEL, B., TRAUT, A. & DU BOIS, A. 2009. Assessment of the sentinel lymph node in patients with invasive squamous carcinoma of the vulva. Acta Obstet Gynecol Scand, 88, 1209-14. ALTMEYERS-ENZYKLOPAEDIE. 2017. Vulva - Altmeyers Enzyklopädie - Fachbereich Dermatologie [Online]. Springer. Available: https://www.enzyklopaedie-dermatologie.de/dermatologie/vulva-23378 - definition [Accessed 10.01.2017 2017]. ATZENDORF, J., RAUSCHERT, C., SEITZ, N. N., LOCHBUHLER, K. & KRAUS, L. 2019. The Use of Alcohol, Tobacco, Illegal Drugs and Medicines. Dtsch Arztebl Int, 116, 577-584. BAANDRUP, L., VARBO, A., MUNK, C., JOHANSEN, C., FRISCH, M. & KJAER, S. K. 2011. In situ and invasive squamous cell carcinoma of the vulva in Denmark 1978–2007—a nationwide population-based study. Gynecologic Oncology, 122, 45-49. BAUMANN, K. H., MULLER, O., NAUJOK, H. B., MANN, E., BARTH, P. & WAGNER, U. 2010. Small-area analysis of incidence and localisation of vulvar cancer. J Oncol, 2010, 512032. BENEDETTI PANICI, P., DI DONATO, V., BRACCHI, C., MARCHETTI, C., TOMAO, F., PALAIA, I., PERNIOLA, G. & MUZII, L. 2014. Modified gluteal fold advancement V-Y flap for vulvar reconstruction after surgery for vulvar malignancies. Gynecol Oncol, 132, 125-9. BLEEKER, M. C., VISSER, P. J., OVERBEEK, L. I., VAN BEURDEN, M. & BERKHOF, J. 2016. Lichen Sclerosus: Incidence and Risk of Vulvar Squamous Cell Carcinoma. Cancer Epidemiol Biomarkers Prev, 25, 1224-30. BUTTMANN-SCHWEIGER, N., KLUG, S. J., LUYTEN, A., HOLLECZEK, B., HEITZ, F., DU BOIS, A. & KRAYWINKEL, K. 2015. Incidence patterns and temporal trends of invasive nonmelanotic vulvar tumors in Germany 1999-2011. A population-based cancer registry analysis. PLoS One, 10, e0128073. COOPER, S. M., ALI, I., BALDO, M. & WOJNAROWSKA, F. 2008. The association of lichen sclerosus and erosive lichen planus of the vulva with autoimmune disease: A case-control study. Archives of Dermatology, 144, 1432-1435. COOPER, S. M., GAO, X. H., POWELL, J. J. & WOJNAROWSKA, F. 2004. Does treatment of vulvar lichen sclerosus influence its prognosis? Arch Dermatol, 140, 702-6. CUNNINGHAM, M. J., GOYER, R. P., GIBBONS, S. K., KREDENTSER, D. C., MALFETANO, J. H. & KEYS, H. 1997. Primary radiation, cisplatin, and 5- fluorouracil for advanced squamous carcinoma of the vulva. Gynecol Oncol, 66, 258-61. DE MELO FERREIRA, A. P., DE FIGUEIREDO, E. M., LIMA, R. A., CÂNDIDO, E. B., DE CASTRO MONTEIRO, M. V., DE FIGUEIREDO FRANCO, T. M. R., TRAIMAN, P. & DA SILVA-FILHO, A. L. 2012. Quality of life in women with vulvar cancer submitted to surgical treatment: a comparative study. European Journal of Obstetrics & Gynecology and Reproductive Biology, 165, 91-95. FABER, M. T., SAND, F. L., ALBIERI, V., NORRILD, B., KJAER, S. K. & VERDOODT, F. 2017. Prevalence and type distribution of human papillomavirus in squamous cell carcinoma and intraepithelial neoplasia of the vulva. Int J Cancer, 141, 1161-1169. FARAGE M.A.; MAIBACH, H. I. May 22, 2017. The Vulva Physiology and Clinical Management, CRC Press, Taylor & Francis Group. FAUL, C. M., MIRMOW, D., HUANG, Q., GERSZTEN, K., DAY, R. & JONES, M. W. 1997. Adjuvant radiation for vulvar carcinoma: improved local control. Int J Radiat Oncol Biol Phys, 38, 381-9. FISTAROL, S. K. & ITIN, P. H. 2013. Diagnosis and Treatment of Lichen Sclerosus. American Journal of Clinical Dermatology, 14, 27-47. FONS, G., GROENEN, S. M., OONK, M. H., ANSINK, A. C., VAN DER ZEE, A. G., BURGER, M. P., STALPERS, L. J. & VAN DER VELDEN, J. 2009. Adjuvant radiotherapy in patients with vulvar cancer and one intra capsular lymph node metastasis is not beneficial. Gynecol Oncol, 114, 343-5. FRUCHTER, R., MELNICK, L. & POMERANZ, M. K. 2017. Lichenoid vulvar disease: A review. International Journal of Women's Dermatology, 3, 58- 64. GAARENSTROOM, K. N., KENTER, G. G., TRIMBOS, J. B., AGOUS, I., AMANT, F., PETERS, A. A. & VERGOTE, I. 2003. Postoperative complications after vulvectomy and inguinofemoral lymphadenectomy using separate groin incisions. Int J Gynecol Cancer, 13, 522-7. GEISLER, J. P., MANAHAN, K. J. & BULLER, R. E. 2006. Neoadjuvant chemotherapy in vulvar cancer: Avoiding primary exenteration. Gynecologic Oncology, 100, 53-57. GOLDSTEIN, A. T., MARINOFF, S. C., CHRISTOPHER, K. & SRODON, M. 2005. Prevalence of vulvar lichen sclerosus in a general gynecology practice. J Reprod Med, 50, 477-80. H.G. SCHNÜRCH, M. H., L.WÖLBER 2018. Tumorerkrankungen der Vulva und Vagina, Springer Verlag. HACKER, N. F., BEREK, J. S., LAGASSE, L. D., LEUCHTER, R. S. & MOORE, J. G. 1983. Management of regional lymph nodes and their prognostic influence in vulvar cancer. Obstet Gynecol, 61, 408-12. HALONEN, P., JAKOBSSON, M., HEIKINHEIMO, O., RISKA, A., GISSLER, M. & PUKKALA, E. 2017. Lichen sclerosus and risk of cancer. International Journal of Cancer, 140, 1998-2002. HAMPL, M., DECKERS-FIGIEL, S., HAMPL, J. A., REIN, D. & BENDER, H. G. 2008a. New aspects of vulvar cancer: changes in localization and age of onset. Gynecol Oncol, 109, 340-5. HAMPL, M., HANTSCHMANN, P., MICHELS, W. & HILLEMANNS, P. 2008b. Validation of the accuracy of the sentinel lymph node procedure in patients with vulvar cancer: Results of a multicenter study in Germany. Gynecologic Oncology, 111, 282-288. HAMPL, M., LANGKAMP, B., LUX, J., KUEPPERS, V., JANNI, W. & MULLERMATTHEIS, V. 2011. The risk of urinary incontinence after partial urethral resection in patients with anterior vulvar cancer. Eur J Obstet Gynecol Reprod Biol, 154, 108-12. HAN, S. C., KIM, D. H., HIGGINS, S. A., CARCANGIU, M. L. & KACINSKI, B. M. 2000. Chemoradiation as primary or adjuvant treatment for locally advanced carcinoma of the vulva. Int J Radiat Oncol Biol Phys, 47, 1235- 44. HEMMINKI, K., LI, X. & VAITTINEN, P. 2002. Time trends in the incidence of cervical and other genital squamous cell carcinomas and adenocarcinomas in Sweden, 1958-1996. Eur J Obstet Gynecol Reprod Biol, 101, 64-9. HOMESLEY, H. D., BUNDY, B. N., SEDLIS, A. & ADCOCK, L. 1986. Radiation therapy versus pelvic node resection for carcinoma of the vulva with positive groin nodes. Obstet Gynecol, 68, 733-40. HOMESLEY, H. D., BUNDY, B. N., SEDLIS, A., YORDAN, E., BEREK, J. S., JAHSHAN, A. & MORTEL, R. 1993. Prognostic factors for groin node metastasis in squamous cell carcinoma of the vulva (a Gynecologic Oncology Group study). Gynecol Oncol, 49, 279-83. IGNATOV, T., EGGEMANN, H., BURGER, E., COSTA, S. D. & IGNATOV, A. 2016. Adjuvant radiotherapy for vulvar cancer with close or positive surgical margins. Journal of Cancer Research and Clinical Oncology, 142, 489-495. IVERSEN, T. & AAS, M. 1983. Lymph drainage from the vulva. Gynecol Oncol, 16, 179-89. IVERSEN, T. & TRETLI, S. 1998. Intraepithelial and invasive squamous cell neoplasia of the vulva: trends in incidence, recurrence, and survival rate in Norway. Obstet Gynecol, 91, 969-72. JACOB, C. V., STELZER, G. T. & WALLACE, J. H. 1980. The influence of cigarette tobacco smoke products on the immune response. The cellular basis of immunosuppression by a water-soluble condensate of tobacco smoke. Immunology, 40, 621-7. JONES, R. W. & JOURA, E. A. 1999. Analyzing prior clinical events at presentation in 102 women with vulvar carcinoma. Evidence of diagnostic delays. J Reprod Med, 44, 766-8. JOURA, E. A., LOSCH, A., HAIDER-ANGELER, M. G., BREITENECKER, G. & LEODOLTER, S. 2000. Trends in vulvar neoplasia. Increasing incidence of vulvar intraepithelial neoplasia and squamous cell carcinoma of the vulva in young women. J Reprod Med, 45, 613-5. JUDSON, P. L., HABERMANN, E. B., BAXTER, N. N., DURHAM, S. B. & VIRNIG, B. A. 2006. Trends in the incidence of invasive and in situ vulvar carcinoma. Obstet Gynecol, 107, 1018-22. KATAOKA, M. Y., SALA, E., BALDWIN, P., REINHOLD, C., FARHADI, A., HUDOLIN, T. & HRICAK, H. 2010. The accuracy of magnetic resonance imaging in staging of vulvar cancer: A retrospective multi-centre study. Gynecologic Oncology, 117, 82-87. KOCH-INSTITUT, R. Berlin, 2017. Krebs in Deutschland für 2013/2014. In: GESELLSCHAFT, R. K.-I. H. U. D. & (HRSG), D. E. K. I. D. E. V. (eds.). KUNOS, C., SIMPKINS, F., GIBBONS, H., TIAN, C. & HOMESLEY, H. 2009. Radiation Therapy Compared With Pelvic Node Resection for Node Positive Vulvar Cancer: A Randomized Controlled Trial. Obstetrics & Gynecology, 114, 537-546. LANDESHAUPTSTADT DÜSSELDORF, A. F. S. U. W. 2017. Statistikabzug aus dem Einwohnermelderegister. LANDRUM, L. M., SKAGGS, V., GOULD, N., WALKER, J. L. & MCMEEKIN, D. S. 2008. Comparison of outcome measures in patients with advanced squamous cell carcinoma of the vulva treated with surgery or primary chemoradiation. Gynecol Oncol, 108, 584-90. LEMINEN, A., FORSS, M. & PAAVONEN, J. 2000. Wound complications in patients with carcinoma of the vulva. Comparison between radical and modified vulvectomies. Eur J Obstet Gynecol Reprod Biol, 93, 193-7. MAGRINA, J. F., GONZALEZ-BOSQUET, J., WEAVER, A. L., GAFFEY, T. A., WEBB, M. J., PODRATZ, K. C. & CORNELLA, J. L. 1998. Primary squamous cell cancer of the vulva: radical versus modified radical vulvar surgery. Gynecol Oncol, 71, 116-21. MAHNER, S., JUECKSTOCK, J., HILPERT, F., NEUSER, P., HARTER, P., DE GREGORIO, N., HASENBURG, A., SEHOULI, J., HABERMANN, A., HILLEMANNS, P., FUERST, S., STRAUSS, H. G., BAUMANN, K., THIEL, F., MUSTEA, A., MEIER, W., DU BOIS, A., GRIEBEL, L. F. & WOELBER, L. 2015. Adjuvant therapy in lymph node-positive vulvar cancer: the AGO-CaRE-1 study. J Natl Cancer Inst, 107. MARTINEZ-PALONES, J. M., PEREZ-BENAVENTE, M. A., GIL-MORENO, A., DIAZ-FEIJOO, B., ROCA, I., GARCIA-JIMENEZ, A., AGUILARMARTINEZ, I. & XERCAVINS, J. 2006. Comparison of recurrence after vulvectomy and lymphadenectomy with and without sentinel node biopsy in early stage vulvar cancer. Gynecol Oncol, 103, 865-70. MELTZER-GUNNES, C. J., SMASTUEN, M. C., KRISTENSEN, G. B., TROPE, C. G., LIE, A. K. & VISTAD, I. 2017. Vulvar carcinoma in Norway: A 50- year perspective on trends in incidence, treatment and survival. Gynecol Oncol, 145, 543-548. MEYRICK THOMAS, R. H., RIDLEY, C. M., MCGIBBON, D. H. & BLACK, M. M. 1988. Lichen sclerosus et atrophicus and autoimmunity--a study of 350 women. Br J Dermatol, 118, 41-6. MITTAG, H. J. 2017. Statistik - Eine Einführung mit interaktiven Elementen, Springer Spektrum, SpringSpringer Spektrum, Berlin, Heidelberger Verlag. OONK, M. H., VAN OS, M. A., DE BOCK, G. H., DE HULLU, J. A., ANSINK, A. C. & VAN DER ZEE, A. G. 2009. A comparison of quality of life between vulvar cancer patients after sentinel lymph node procedure only and inguinofemoral lymphadenectomy. Gynecol Oncol, 113, 301-5. PINTO, A. P., MIRON, A., YASSIN, Y., MONTE, N., WOO, T. Y., MEHRA, K. K., MEDEIROS, F. & CRUM, C. P. 2010. Differentiated vulvar intraepithelial neoplasia contains Tp53 mutations and is genetically linked to vulvar squamous cell carcinoma. Mod Pathol, 23, 404-12. POLTERAUER, S., SCHWAMEIS, R., GRIMM, C., MACUKS, R., IACOPONI, S., ZALEWSKI, K. & ZAPARDIEL, I. 2017. Prognostic value of lymph node ratio and number of positive inguinal nodes in patients with vulvar cancer. Gynecologic Oncology, 147, 92-97. RAKISLOVA, N., SACO, A., SIERRA, A., DEL PINO, M. & ORDI, J. 2017. Role of Human Papillomavirus in Vulvar Cancer. Advances in Anatomic Pathology, 24, 201-214. REYES, M. C. & COOPER, K. 2014. An update on vulvar intraepithelial neoplasia: terminology and a practical approach to diagnosis. J Clin Pathol, 67, 290-4. ROTTMANN, M., BECK, T., BURGES, A., DANNECKER, C., KIECHLE, M., MAYR, D., SCHLESINGER-RAAB, A., SCHUBERT-FRITSCHLE, G. & ENGEL, J. 2016. Trends in surgery and outcomes of squamous cell vulvar cancer patients over a 16-year period (1998–2013): a populationbased analysis. Journal of Cancer Research and Clinical Oncology, 142, 1331-1341. SAGDEO, A., GORMLEY, R. H., ABUABARA, K., TYRING, S. K., RADY, P., ELDER, D. E. & KOVARIK, C. L. 2014. The diagnostic challenge of vulvar squamous cell carcinoma: Clinical manifestations and unusual human papillomavirus types. J Am Acad Dermatol, 70, 586-8. SCHIFFMAN, M. H. & CASTLE, P. 2003. Epidemiologic Studies of a Necessary Causal Risk Factor: Human Papillomavirus Infection and Cervical Neoplasia. JNCI: Journal of the National Cancer Institute, 95, E2-E2. SCHNURCH, H. G., ACKERMANN, S., ALT, C. D., BARINOFF, J., BOING, C., DANNECKER, C., GIESEKING, F., GUNTHERT, A., HANTSCHMANN, P., HORN, L. C., KURZL, R., MALLMANN, P., MARNITZ, S., MEHLHORN, G., HACK, C. C., KOCH, M. C., TORSTEN, U., WEIKEL, W., WOLBER, L. & HAMPL, M. 2016. Diagnosis, Therapy and Follow-up Care of Vulvar Cancer and its Precursors. Guideline of the DGGG and DKG (S2k-Level, AWMF Registry Number 015/059, November 2015. Geburtshilfe Frauenheilkd, 76, 1035-1049. SCHÜNKE M, S. E., SCHUMACHER U ET AL. 2018. Prometheus LernAtlas - Allgemeine Anatomie und Bewegungssystem. SCHUURMAN, M. S., VAN DEN EINDEN, L. C. G., MASSUGER, L. F. A. G., KIEMENEY, L. A., VAN DER AA, M. A. & DE HULLU, J. A. 2013. Trends in incidence and survival of Dutch women with vulvar squamous cell carcinoma. European Journal of Cancer, 49, 3872-3880. SOLIMAN, A. A., HEUBNER, M., KIMMIG, R. & WIMBERGER, P. 2012. Morbidity of inguinofemoral lymphadenectomy in vulval cancer. ScientificWorldJournal, 2012, 341253. STANLEY, M. 2010. Pathology and epidemiology of HPV infection in females. Gynecologic Oncology, 117, S5-S10. STIKO:, A. H. D. S. I. 2018. Wissenschaftliche Begründung für die Empfehlung der HPV-Impfung für Jungen im Alter von 9 bis 14 Jahren. Epid Bull 2018;26:233 – 250. THANH, H. D., AMY, A. H., STEPHEN, J. L., MARK, T. W., ROBERT, J. M. & ERNEST, S. H. 2017. Surgical Management of Vulvar Cancer. Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw, 15, 121-128. VAN DER LINDEN, M., SCHUURMAN, M., BULTEN, J., VAN DER AA, M., MASSUGER, L. & DE HULLU, J. 2017. Incidence and survival of glandular vulvar malignancies in the Netherlands. Gynecol Oncol, 144, 553-557.VISWANATHAN, C., KIRSCHNER, K., TRUONG, M., BALACHANDRAN, A., DEVINE, C. & BHOSALE, P. 2013. Multimodality imaging of vulvar cancer: staging, therapeutic response, and complications. AJR Am J Roentgenol, 200, 1387-400. WASSERSTEIN, R. L. & LAZAR, N. A. 2016. The ASA's Statement on p- Values: Context, Process, and Purpose. The American Statistician, 70, 129-133. WILKINSON, E. J., RICO, M. J. & PIERSON, K. K. 1982. Microinvasive carcinoma of the vulva. International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists, 1, 29-39. WILLS, A. & OBERMAIR, A. 2013. A review of complications associated with the surgical treatment of vulvar cancer. Gynecologic Oncology, 131, 467- 479. WITTEKIND, C. 2017. TNM Klassifikation maligner Tumoren Wiley-VCH. WOELBER, L., EULENBURG, C., CHOSCHZICK, M., KRUELL, A., PETERSEN, C., GIESEKING, F., JAENICKE, F. & MAHNER, S. 2012a. Prognostic role of lymph node metastases in vulvar cancer and implications for adjuvant treatment. Int J Gynecol Cancer, 22, 503-8. WOELBER, L., EULENBURG, C., CHOSCHZICK, M., KRUELL, A., PETERSEN, C., GIESEKING, F., JAENICKE, F. & MAHNER, S. 2012b. Prognostic Role of Lymph Node Metastases in Vulvar Cancer and Implications for Adjuvant Treatment. International Journal of Gynecological Cancer, 22, 503-508. WOELBER, L., JAEGER, A. & PRIESKE, K. 2020. New treatment standards for vulvar cancer 2020. Curr Opin Obstet Gynecol, 32, 9-14. ZEE, A. G. V. D., OONK, M. H., HULLU, J. A. D., ANSINK, A. C., VERGOTE, I., VERHEIJEN, R. H., MAGGIONI, A., GAARENSTROOM, K. N., BALDWIN, P. J., DORST, E. B. V., VELDEN, J. V. D., HERMANS, R. H., PUTTEN, H. V. D., DROUIN, P., SCHNEIDER, A. & SLUITER, W. J. 2008. Sentinel node dissection is safe in the treatment of early-stage vulvar cancer. Journal of Clinical Oncology, 26, 884-889. ZUR HAUSEN, H. 2002. Papillomaviruses and cancer: from basic studies to clinical application. Nat Rev Cancer, 2, 342-50. | |||||||
Lizenz: | Urheberrechtsschutz | |||||||
Fachbereich / Einrichtung: | Medizinische Fakultät | |||||||
Dokument erstellt am: | 11.11.2020 | |||||||
Dateien geändert am: | 11.11.2020 | |||||||
Promotionsantrag am: | 10.08.0020 | |||||||
Datum der Promotion: | 03.11.2020 |