medigraphic.com
SPANISH

Correo Científico Médico de Holguín

ISSN 1560-4381 (Print)
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2017, Number 3

Next >>

Correo Científico Médico 2017; 21 (3)

Surgical treatment in pilonidal fistulas in follicular occlusion syndrome

Rojas BR, Martínez VG, Fornet FR, Bauta DJL, Rodríguez LML
Full text How to cite this article

Language: Spanish
References: 19
Page: 707-719
PDF size: 455.38 Kb.


Key words:

acne inverse, acne conglobata, pilonidal fistula.

ABSTRACT

Introduction: follicular occlusive syndrome includes inverse acne, acne conglobata and pilonidal fistula (triad); when it is associated to the dissecting folliculitis of the scalp then it constitutes the tetrad of follicular occlusion. Reverse acne is a suppurative, chronic and invalidating disease. Its clinical features are the presence of comedones with multiple openings that link two or more follicles, abscesses with epithelial communications, and draining sinuses in regions with apocrine glands. The genesis of these affections is basically genetic with dermatological expression.
Objective: to describe physically and histopathologically the patients with follicular occlusion syndrome, as well as the results of surgical treatment of pilonidal fistula in this disorder.
Method: the study is on the prevalence of pilonidal fistula in follicular occlusion syndrome in 37 patients with follicular occlusion syndrome. The local excision of the pilonidal and perianal fistulas was performed, this exeresis extended by the subcutaneous cellular tissue until the facia. The area was then repaired with a skin-free graft.
Results: four patients had the pilonidal fistula, with long periods of evolution, who were treated with autograft of skin. Hyperkeratosis, as well as, perifolliculitis were the most relevant histopathological changes.
Conclusion: the pilonidal fistula is difficult for follicular occlusion syndrome management and only the surgical treatment is the most suitable.


REFERENCES

  1. Kaminsky A. Síndrome de oclusión de los folículos terminales (Acné Inversa). Terap Dermatol. 2007 [citada 12 abr 2009]; 30:78-90. Disponible en: http://www.atdermae.com/pdfs/atd_30_02_02.pdf

  2. Fitzsimmons JS, Fitzsimons EM, Gilbert G. Familial hidradenitis suppurativa: evidence in favour of single gene transmission. J Med Genet. 1984[citada 12 abr 2009]; 21(4):281-285. Disponible en: www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1049298

  3. Prasad PV, Kaviarasan PK, Joseph JM, Madhuri S, Viswanathan P. Familial acne inversa with acne conglobata in three generations. Indian J Dermatol Venereol Leprol. 2008 [citada 12 abr 2009]; 74(3):283-285. Disponible en: http://www.ijdvl.com/text.asp?2008/74/3/283/41395

  4. Li CR, Jiang MJ, Shen BD, Xu HX, Wang HS, Yao X, et al. Two novel mutations of the nicastrin gene in Chinese patients with acne inversa. Br J Dermatol. 2011 [citado 15 dic 2014]; 165(2):415–418. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.2011.10372.x/abstract;jsessionid=B03644305219D7CF895F44C11172916D.f03t01

  5. Wang B, Yang W, Wen B, Sun J, Su B, Liu B, et al. γ-Secretase Gene Mutations in Familial Acne Inversa. Science. 2010[citado 15 dic 2014];330(6007):1056. Disponible en: http://www.hidradenitis.eu/files/ref1.pdf

  6. Liu Y, Gao M, Lv YM, Yang X, Ren YQ, Jiang T, et al. Confirmation by exome sequencing of the pathogenic role of NCSTN mutations in acne inversa (hidradenitis suppurativa). J Invest Dermatol. 2011[citado 15 dic 2014];131(7):1570–1572. Disponible en: http://www.sciencedirect.com/science/article/pii/S0022202X15353185

  7. Nomura Y, Nomura T, Sakai K, Sasaki K, Ohguchi Y, Mizuno O, et al. A novel splice site mutation in NCSTN underlies a Japanese family with hidradenitis suppurativa.Br J Dermatol. 2013 [citado 15 dic 2014]; 168(1):206–209.Disponible en:http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.2012.11174.x/abstract

  8. Pink AE, Simpson MA, Brice GW, Smith CH, Desai N, Mortimer PS, et al. PSENEN and NCSTN mutations in familial hidradenitis suppurativa (Acne Inversa). J Invest Dermatol. 2011 [citado 15 dic 2014]; 131(7):1568–1570. Disponible en: http://www.sciencedirect.com/science/article/pii/S0022202X15353227

  9. Fimmel S, Zouboulis CC.Comorbidities of hidradenitis suppurativa (acne inversa). Dermatoendocrinol. 2010[citado 15 dic 2014]; 2(1):9-16. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084959/pdf/de0201_0009.pdf

  10. Jansen I, Altmeyer P, Piewig G. Acne inversa (alias hidradenitis suppurativa). J Eur Acad Dermatol Venereol. 2001 [citado 15 dic2014]; 15(6):532-540. Disponible en: http://onlinelibrary.wiley.com/doi/10.1046/j.1468-3083.2001.00303.x/full

  11. Sellheyer K, Krahl D. “Hidradenitis suppurativa” is acne inversa! An appeal to (finally) abandon a misnomer. Int J Dermatol. 2005 [citado 15 dic 2014]; 44(7): 535–540. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-4632.2004.02536.x/full

  12. Von Laffert M, Stadie V, Wohlrab J, Marsch WC. Hidradenitis suppurativa/acne inversa: bilocated epithelial hyperplasia with very different sequelae. Br J Dermatol. 2011 [citado 15 de diciembre 2014]; 164(2):367-71. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.2010.10034.x/full

  13. Gao M, Wang PG, Cui Y, Yang S, Zhang YH, Lin D, et al. Inversa Acne (Hidradenitis Suppurativa): A Case Report and Identification of the Locus at Chromosome 1p21.1–1q25.3. J Invest Dermatol. 2006 [citado 15 dic 2014]; 126(6):1302-1306. Disponible en: http://www.sciencedirect.com/science/article/pii/S0022202X15329444

  14. Al-Ali FM, Ratnamala U, Mehta TY, Naveed M, Al-Ali MT, Al-Khaja N, et al. Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region. Exp Dermatol. 2010 [citado 15 dic 2014]; 19(9):851–853. Disponible en: http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0625.2010.01088.x/full

  15. Hamosh A, Scott AF, Amberger JS, Bocchini CA, McKusick VA. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res. 2005 [citado 15 dic 2014]; 33(Suppl 1): 514-517. Disponible en: https://academic.oup.com/nar/article/33/suppl_1/D514/2505259/Online-Mendelian-Inheritance-in-Man-OMIM-a

  16. Ingram JR, Piguet V. Phenotypic heterogeneity in hidradenitis suppurativa (acne inversa): classification is an essential step toward personalized therapy. J Invest Dermatol. 2013 [citado 15 dic 2014]; 133(6):1453-1456.Disponible en: http://ac.els-cdn.com/S0022202X15362977/1-s2.0-S0022202X15362977-main.pdf?_tid=258dd4c2-e97a-11e6-9f7e-00000aab0f01&acdnat=1486062330_23cb44c3a7a17fefafd9cc909e034b00

  17. Pagano A, Feldman MJ. Management of chronic gluteal follicular occlusive disease. Eplasty. 2013[citado 15 dic 2014]; 13.Disponible en: http://www.eplasty.com/index.php?option=com_content&view=article&id=973&catid=49

  18. Jain K, Jain VK, Aggarwal K, Bansal A. Late onset isotretinoin resistant acne conglobata in a patient with acromegaly. Indian J Dermatol Venereol Leprol. 2008 [citado 15 dic 2014]; 74(2):139-141. Disponible en: http://www.ijdvl.com/article.asp?issn=0378-6323;year=2008;volume=74;issue=2;spage=139;epage=141;aulast=Jain

  19. Orozco B, Campo ME, Anaya LA, Atuesta J, Ávila JM, Balcázar LF. Guías colombianas para el manejo del acné: una revisión basada en la evidencia por el Grupo Colombiano de Estudio en Acné. Rev Asoc Colombiana Dermatol. 2011 [citado 15 de diciembre 2014]; 19: 129-158. Disponible en: http://docplayer.es/4394597-Guias-colombianas-para-el-manejo-del-acne-una-revision-basada-en-la-evidencia-por-el-grupo-colombiano-de-estudio-en-acne.htm




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Correo Científico Médico. 2017;21