CLINICAL CASE OF PALMOPLANTAR KERATODERMA TYPE UNNA-THOST


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Abstract

Palmar-plantar keratoderma is a heterogeneous group of hereditary dermatosis, which can be independent diseases or combined with various congenital malformations, most of ectodermal origin. Approaches to differential diagnosis and clinical features of each form of this pathology are described. Keratoderma, Unna Toast genodermatosis belongs to the group, which is characterized by hyperkeratosis on the palms and soles without migration to other skin areas.

About the authors

Albina G. Pashinyan

N.I. Pirogov Russian National Research Medical University

Email: stsoagp4@gmail.com
MD, PhD, DSc, prof. of N.I. Pirogov Russian National Research Medical University, Moscow, 117997, Russian Federation Moscow, 117997, Russian Federation

L. I Ilienko

N.I. Pirogov Russian National Research Medical University

Moscow, 117997, Russian Federation

A. N Akopyan

N.I. Pirogov Russian National Research Medical University

Moscow, 117997, Russian Federation

References

  1. Itin P.H., Fistarol S.K. Palmoplantar keratodermas. Clin. Dermatol. 2005; 23(1): 15-22.
  2. Allan C.M., Procaccia S., Tran D., Tu Y., Barnes R.H., Larsson M., et al. Palmoplantar keratoderma in slurp2-deficient mice. J. Invest. Dermatol. 2016; 136(2): 436-43. doi: 10.1016/j.jid.2015.11.003
  3. Nomura T., Mizuno O., Miyauchi T., Suzuki S., Shinkuma S., Hata H., et all Striate palmoplantar keratoderma: Report of a novel DSG1 mutation and atypical clinical manifestations. J. Dermatol. Sci. 2015; 80(3): 223-5. doi: 10.1016/j.jdermsci.2015.10.004.
  4. Stypczyńska E., Placek W., Zegarska B., Czajkowski R. Keratinization disorders and genetic aspects in palmar and plantar keratodermas. Acta Dermatovenerol. Croat. 2016; 24(2): 116-23.
  5. Sakiyama T., Kubo A. Hereditary palmoplantar keratoderma “clinical and genetic differential diagnosis”. J. Dermatol. 2016; 43(3): 264-74. doi: 10.1111/1346-8138.13219.
  6. Sehgal V.N., Aggarwal A,. Syed N.H., Rasool F., Verma P., Sharma S. Palmoplantar keratoderma as a variant of lichen planus. Skinmed. 2016; 14(1): 56-60.
  7. Kim J., Foster R., Lam M., Kumarasinghe S.P. Mycosis fungoides: an important differential diagnosis for acquired palmoplantar keratoderma. Australas J. Dermatol. 2015; 56(1): 49-51. doi: 10.1111/ajd.12155.
  8. Hersle K., Mobacken H. Hyperkeratotic dermatitis of the palms. Br. J. Dermatol. 1982; 107(2): 195-201.
  9. Küster W., Becker A. Indication for the identity of palmoplantar keratoderma type Unna-Thost with type Vörner. Thost’s family revisited 110 years later. Acta Derm. Venereol. 1992; 72(2): 120-2.
  10. Perez C., Khachemoune A. Mal de Meleda: a focused review. Am. J. Clin. Dermatol. 2016; 17(1): 63-70. doi: 10.1007/s40257-015-0157-1.
  11. Jijin M.J., Jaishankar H.P., Narayaran V.S., Rangaswamy K., Puthaswamy K.A. Papillon-Lefevre syndrome in an adolescent female: a case study. Clin. Diagn. Res. 2015; 9(5): 23-5. doi: 10.7860/JCDR/2015/12780.5921.
  12. Bragg J., Rizzo C., Mengden S. Striate palmoplantar keratoderma (Brunauer-Fohs-Siemens syndrome). Dermatol. Online J. 2008; 14(5): 26.
  13. Schiller S., Seebode C., Hennies H., Giehl K., Emmert S. Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease. J. Dtsch. Dermatol. Ges. 2014; 12(9): 781-8. doi: 10.1111/ddg.12418.
  14. Antonio J.R., Oliveira G.B., Rossi N.C., Pires L.G. Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient. An Bras. Dermatol. 2014; 89(5): 819-21.
  15. Ramos-E-Silva M., Carvalho J.C., Carneiro S.C. Cutaneous paraneoplasia. Clin. Dermatol. 2011; 29(5): 541-7.
  16. Hu W., Cook T.F., Vicki G.J., Glaser D.A. Acrokeratoelastoidosis. Pediatr. Dermatol. 2002; 19(4): 320-2.
  17. Белоусова Т.А., Теплюк Н.П., Филиппова В.А., Мельниченко А.Б. Гиперкератотические наслоения на коже ладоней и подошв. Российский журнал кожных и венерических болезней. 2009; 12(5): 48-9
  18. Mofid MZ, Costarangos C, Gruber SB, Koch SE. Hereditary epidermolytic palmoplantar keratoderma (Vörner type) in a family with Ehlers-Danlos syndrome. J. Am. Acad. Dermatol. 1998; 38(5, Pt 2): 825-30.
  19. Kuster W., Reis A., Hennies H.C. Epidermolytic palmoplantar keratoderma of Vorner: re-evaluation of Vorner’s original family and identification of a novel keratin 9 mutation. Arch. Dermatol. Res. 2002; 294(6): 268-72.
  20. Sehgal V.N., Sardana K., Sharma S., Raut D. Hereditary palmoplantar (epidermolytic) keratoderma: illustration through a familial report. Skinmed. 2004; 3(6): 323-30.
  21. Bakija-Konsuo A. Mal de Meleda - through history and today. Acta Dermatovenerol. Croat. 2014; 22(2): 79-84.
  22. Iqtadar S., Mumtaz S.U., Abaidullah S. Papillon-Lèfevre syndrome with palmoplantar keratoderma and periodontitis, a rare cause of pyrexia of unknown origin: a case report. J. Med. Case Rep. 2015; 9: 288. doi: 10.1186/s13256-015-0773-7.
  23. Janjua S.A., Khachemoune A. Papillon-Lefevre syndrome: case report and review of the literature. Dermatol. Online J. 2004; 10(1): 13.
  24. Mallo S., Bernal A.I., Fernández-Canedo M.I., González-Hermoso C., de Troya-Martín M. Autosomal dominant punctate palmoplantar keratoderma. Actas Dermosifiliogr. 2006; 97(2): 136-8.
  25. Oztas P., Alli N., Polat M., Dagdelen S., Ustün H., Artüz F., Erdemli E. Punctate palmoplantar keratoderma (Brauer-Buschke-Fischer Syndrome). Am. J. Clin. Dermatol. 2007; 8(2): 113-6.
  26. Nair P.A. Dermatosis associated with menopause. J. Midlife Health. 2014; 5(4): 168-75. doi: 10.4103/0976-7800.145152
  27. Erkek E., Koçak M., Bozdoğan O., Atasoy P., Birol A. Focal acral hyperkeratosis: a rare cutaneous disorder within the spectrum of Costa acrokeratoelastoidosis. Pediatr. Dermatol. 2004; 21(2): 128-30.

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