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Referat HS (1) .PPTX Revisi
Referat HS (1) .PPTX Revisi
Staphylococcus aureus
Risk Factor :
1. Genetic
2. Hormon
3. Obesity
4. Bacterial infection
5. Smoking
Kang Sewon, et al. Fitzpatrick’s Dermatology, 9th edition. US: Mc Graw Hill Educaton. 2019
Pathogenesis
Apocrine occlusion (keratin occlusion)
Hidradenitis suppurativa and metabolic syndrome: a comparative cross-sectional study of 3207 patients.Shalom G, Freud T, Harman-Boehm I, Polishchuk I, Cohen AD Br J Dermatol. 2015 Aug; 173(2):464-70.
Psychosocial impact of hidradenitis suppurativa: a qualitative study.Esmann S, Jemec GB Acta Derm Venereol. 2011 May; 91(3):328-32
Clinical Manifestation
Fimmel S and Zouboulrs CC. Cormobities of Hidradenitis Suppurativa (Acne Inversa). Dermatoendocrinol.2010 Jan-Mar; 2(1): 9-16. Available from URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084959/?tool=pmcentrez. Accesed on December 1st, 2019.
Hurley Classification
Grade I Grade II Grade III
Solitary or multiple abscesses witho Recurrent abscesses, solitary or Diffuse or extensive invol-vement of
ut a matrix or sinus multiple lesions that are far apart, the surrounding area with sinuses a
with sinuses nd interconnected abscesses
Fimmel S and Zouboulrs CC. Cormobities of Hidradenitis Suppurativa (Acne Inversa). Dermatoendocrinol.2010 Jan-Mar; 2(1): 9-16. Available from URL:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084959/?tool=pmcentrez. Accesed on December 1st, 2019.
Supporting Examination
Fite D. Hidradenitis Suppurativa in Emergency Medicine. May 2010. Emedicine. Available from URL: http://emedicine.medscape.com/article/762444-overview. Accesed
on December 2nd, 2019.
sofyan, M.A.2013 Hidradenitis Suppurativa. In Wolff K., Goldsmith, L.A., Katz, S.I. Gilcherts, B.A., Paller, A.S., Lefell, D.J.(Eds) ’Fitzpatrick’s Dermatology in
General Medicine’ Volume I. 7th Edition. USA: McGraw-Hill
Differential diagnosis
Wolff K, Goldsmith LA, Katz SI, et al. Fitzpatrick’s Dermatology in General Medicine, 7th edition. US: Mc Graw Hill Medical. 2008. Pyoderma: Hidradenitis. Dalam
Adhi Djuanda (Ed). Ilmu Penyakit Kulit dan Kelamin Edisi ke-7. Jakarta : FKUI.
Treatments
Non-pharmacologic :
• If obese or overweight, weight reduction
• Reduce friction by wearing loose-fitting clothing,
• Heat avoidance.
• Antiseptic soaps
• Smoking cessation
James WD, Elston DM, et al. Andrews’ Disease of the Skin Clinical Dermatology, 13th edition
Medical therapy
Topical Oral
Early inflammatory lesions : steroid Antobiotic : clindamycin and
therapy Intralesional rifampin (300 mg / 2 to 3 times daily)
triamcinolone (5 mg/ml) or Eritromycin, tetracyclin,
minocycline
Clindamycin 1 % lotion applied twice
daily Corticosteroid oral ( severe case )
Kang Sewon, et al. Fitzpatrick’s Dermatology, 9th edition. US: Mc Graw Hill Educaton. 2019
Prognosis
The severity of this disease varies greatly. Many patients only
experience mild symptoms, HS usually experiences spontaneous
remission at age> 35 years.
• starts at or soon after puberty, women are affected three times as often as men.