Gorlin-Goltz syndrome


Authors: V. Bartoš 1;  M. Kullová 2;  K. Adamicová 3;  I. Paučinová 4
Authors place of work: Oddelenie patologickej anatómie, FNsP Žilina 1;  Dermatovenerologický stacionár, FNsP Žilina 2;  Ústav patologickej anatómie, JLF UK a UN Martin 3;  Oddelenie lekárskej genetiky, FNsP Žilina 4
Published in the journal: Klin Onkol 2019; 32(2): 124-128
Category: Kazuistika
doi: 10.14735/amko2019124

Summary

Background:

Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by a predisposition to various cancers. Clinicopathological findings of syndrome are very diverse and many symptoms begin to manifest in a certain period of life.

Case:

The authors describe a case report of a man who, at the age of 34 years, presented to a dermatologist with multiple tumor lesions of the skin. The lesions started to develop when he was 30 years old and thereafter increased in number. Histology revealed superficial, superficial-nodular and nodular basal cell carcinomas. A total of 11 basal cell carcinomas were surgically removed and microscopically investigated. The others were treated locally with imiquimod cream and cryotherapy. In addition, he was found to have multiple odontogenic keratocysts in the jaw and mandible, as well as supernumerary and retinated teeth. Stomatologic and maxillofacial surgery interventions were performed. Further clinical and imaging examinations confirmed macrocephaly, hypertelorism, calcification of falx cerebri, and abnormalities of the cervical vertebrae. The spectrum of pathological findings met the diagnostic criteria of Gorlin-Goltz syndrome.

Conclusion:

Although Gorlin-Goltz syndrome is very rare in routine practice, it usually represents a serious disease with multiple organ system involvement. From a prognostic point of view, early diagnosis with adequate therapy is critical. If a diagnosis is confirmed, lifetime dispensary care with interdisciplinary medical cooperation is necessary.

The authors would like to thank all physicians who participated in the diagnostics and therapy of the presented patient.

The authors declare they have no potential confl icts of interest concerning drugs, products, or services used in the study.

The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.

Submitted: 30. 8. 2018

Accepted: 8. 1. 2019

Keywords:

Gorlin-Goltz syndrome – basal cell carcinoma – odontogenic cysts


Zdroje

1. Krutílková V. Genetické syndromy predisponující k dětským nádorům centrálního nervového systému. Klin Onkol 2016; 29 (Suppl 1): S71–S77. doi: 10.14735/amko2016S71.

2. Plevová P, Krutílková V, Puchmajerová A et al. Gorlinův syndrom. Klin Onkol 2009; 22 (Suppl 1): S34–S35.

3. Plevová P, Šilhánová E, Foretová L et al. Vzácné hereditární syndromy s vyšším rizikem vzniku nádorů. Klin Onkol 2006; 19 (Suppl 1): S68–S75.

4. Gorlin RJ, Goltz RW. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome. N Eng J Med 1960; 262: 908–912. doi: 10.1056/NEJM196005052621803.

5. Kimonis VE, Goldstein AM, Pastakia B et al. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. Am J Med Genet 1997; 69 (3): 299–308.

6. Thomas N, Vinod SV, George A et al. Gorlin–Goltz syndrome: an often missed diagnosis. Ann Maxillofac Surg 2016; 6 (1): 120–124. doi: 10.4103/ 2231-0746.186148.

7. Visioli F, Martins CA, Heitz C et al. Is nevoid basal cell carcinoma syndrome really so rare? Proposal for an investigative protocol based on a case series. J Oral Maxillofacial Surg 2010; 68 (4): 903–908. doi: 10.1016/j.joms.2009.03.032.

8. Endo M, Fujii K, Sugita K et al. Nationwide survey of nevoid basal cell carcinoma syndrome in Japan revealing the low frequency of basal cell carcinoma. Am J Med Genet A 2012; 158A (2): 351–357. doi: 10.1002/ajmg.a.34421.

9. Shanley S, Ratcliffe J, Hockey A et al. Nevoid basal cell carcinoma syndrome: review of 118 affected individuals. Am J Med Genet 1994; 50 (3): 282–290. doi: 10.1002/ajmg.1320500312.

10. Evans DG, Howard E, Giblin C et al. Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic service. Am J Med Genet A 2010; 152A (2): 327–332. doi: 10.1002/ajmg.a.33139.

Štítky
Dětská onkologie Chirurgie všeobecná Onkologie

Článek vyšel v časopise

Klinická onkologie

Číslo 2

2019 Číslo 2

Nejčtenější v tomto čísle

Tomuto tématu se dále věnují…


Kurzy

Zvyšte si kvalifikaci online z pohodlí domova

Zánětlivá bolest zad a axiální spondylartritida – Diagnostika a referenční strategie
nový kurz
Autoři: MUDr. Monika Gregová, Ph.D., MUDr. Kristýna Bubová

Inhibitory karboanhydrázy v léčbě glaukomu
Autoři: as. MUDr. Petr Výborný, CSc., FEBO

Příběh jedlé sody
Autoři: MUDr. Ladislav Korábek, CSc., MBA

Krvácení v důsledku portální hypertenze při jaterní cirhóze – od pohledu záchranné služby až po závěrečný hepato-gastroenterologický pohled
Autoři: PhDr. Petr Jaššo, MBA, MUDr. Hynek Fiala, Ph.D., prof. MUDr. Radan Brůha, CSc., MUDr. Tomáš Fejfar, Ph.D., MUDr. David Astapenko, Ph.D., prof. MUDr. Vladimír Černý, Ph.D.

Rozšíření možností lokální terapie atopické dermatitidy v ordinaci praktického lékaře či alergologa
Autoři: MUDr. Nina Benáková, Ph.D.

Všechny kurzy
Kurzy Doporučená témata Časopisy
Přihlášení
Zapomenuté heslo

Nemáte účet?  Registrujte se

Zapomenuté heslo

Zadejte e-mailovou adresu se kterou jste vytvářel(a) účet, budou Vám na ni zaslány informace k nastavení nového hesla.

Přihlášení

Nemáte účet?  Registrujte se