CASE REPORT
Combination therapy of basal-cell carcinoma in 31-year-old patient with nevoid basal cell carcinoma syndrome – Case study
1
NZOZ Med-Laser Lublin, Poland
2
Chair and Department of Dermatology, Venerology and Paediatric Dermatology, Lublin, Poland
3
Independent Public Teaching Hospital No. 1 in Lublin, Poland
4
Chair and Department of Pathophysiology, Medical University of Lublin, Poland
Corresponding author
Monika Dudra-Jastrzębska
Chair and Department of Pathophysiology, Medical University of Lublin, Jaczewskiego 8b, 20-090 Lublin, Poland
Chair and Department of Pathophysiology, Medical University of Lublin, Jaczewskiego 8b, 20-090 Lublin, Poland
J Pre Clin Clin Res. 2016;10(1):66-68
KEYWORDS
ABSTRACT
Nevoid basal cell carcinoma syndrome (NBCCS) is a rare genetic disease that is manifested in a number of disorders concerning the skin, skeleton, cardiovascular and nervous systems. Various defects which can be observed at first contact with a patient visiting a dermatologist or dentist may help to diagnose this syndrome. Frequent problems with odontogenic cysts and metastatic basal-cell carcinomas result in patients being under the constant care of a specialist. This short study presents the case of 31-year-old patient with Gorlin-Goltz syndrome treated with combination therapy using CO2 laser and photodynamic therapy.
REFERENCES (11)
1.
Burdgorf WHC, Plewing G, Wolff HH, Landhaler M. (ed.). Braun- FalcoDermatologia. [In:] Rak podstawnokomórkowy. Reifenberg J, Ruzicka T. Wydawnictwo Czelej, Lublin, 2011: 1378–1379.
2.
Dobrzańska A, Ryżko J. (ed.). Pediatria. [In:] Genetyka. Krajewska- Walasek M. Urban & Partner, Wrocław, 2004: 56–57.
3.
Daneswari M, Reddy MSR. Genetic mutations in Gorlin-Goltz syndrome. Indian J Hum Genet. 2013 Jul-Sep; 19(3): 369–372.
4.
Szporek B, Kuśnierczyk-Grochowina D, Cieślik T. Badanie cefalometryczne w zespole Gorlina. Dent Med Probl. 2003; 40(2): 411–415.
5.
Pandeshwar P, Jayanthi K, Mahesh D. Gorlin-Goltz Syndrome. Case Rep Dent. 2012, art 247239.
6.
Agrawal A, Murari A, Vutukuri S, Singh A. Gorlin-GoltzSyndrome: Case report of a Rare Hereditary Disorder. Case Rep Dent. 2012, art 475439.
7.
Pirshner F, Bastos PM, Contarato GL, Bon Lima Bimbato AC, Filho AC. Gorlin syndrome and bilateral ovarian fibroma. Int J Surg Case Rep. 2012; 3(9): 477–480.
8.
Kiwilsza M, Sporniak-Tutak K. Gorlin-Goltz syndrome-a medical condition requiring a multidisciplinary approach. Med Sci Monit. 2012; 18(9): 145–153.
9.
Stern RS. Cost effectiveness of Mohs Micrographic Surgery. J Invest Dermatol. 2013; 133: 1129–1131.
10.
Paoli J, Daryoni S, Wennberg AM, Molnie L, Gillstedt M, Miocic M, Stenquist B. 5-year Recurrence Rates of Mohs Micrographic Surgery for Aggressive and Recurrent Facial Basal Cell Carcinoma. Acta Derm Venereol. 2011 Oct; 91(6): 689–93.
11.
Piłat P, Borzęcki A, Krasowska D. Rozległa choroba Bowena twarzy – leczenie skojarzone. Przegl Dermatol. 2014; 101: 201–204.
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| eISSN: | 1898-7516 |
| ISSN: | 1898-2395 |
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