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A Case of Multiple Necrotic Dyskeratotic Cells within the Upper Epidermis and Horny Layer Revealing Persistent Papules and Plaques of Adult-Onset Still’s Disease

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초록

It is important to differentiate violaceous to dusky red papules and plaques that widely persist on the trunk and extremities because there are dermatoses that could be fatal, such as lupus erythematosus, dermatomyositis, drug eruptions, and graft-versus-host disease. Dyskeratotic cells only in the upper epidermis and horny layer are not well known, but it is a distinctive histopathological pattern of atypical type of rash of adult-onset Still’s disease (AOSD). AOSD rash is a transient salmon-colored rash that occurs and disappears with fever; however, an atypical type of rash called “persistent dermal plaque” or “persistent pruritic eruptions” has also been reported. It occurs and persists even after fever subsides. Herein, we describe a case with necrotic dyskeratotic cells in the upper epidermis and horny layer without AOSD symptoms lasting for five years.

Abstract

It is important to differentiate violaceous to dusky red papules and plaques that widely persist on the trunk and extremities because there are dermatoses that could be fatal, such as lupus erythematosus, dermatomyositis, drug eruptions, and graft-versus-host disease. Dyskeratotic cells only in the upper epidermis and horny layer are not well known, but it is a distinctive histopathological pattern of atypical type of rash of adult-onset Still’s disease (AOSD). AOSD rash is a transient salmon-colored rash that occurs and disappears with fever; however, an atypical type of rash called “persistent dermal plaque” or “persistent pruritic eruptions” has also been reported. It occurs and persists even after fever subsides. Herein, we describe a case with necrotic dyskeratotic cells in the upper epidermis and horny layer without AOSD symptoms lasting for five years.

참고문헌 (13)

  1. Gru AA, "Lichenoid and interface dermatoses", Semin Diagn Pathol, 34, pp.237~249 (2017)
  2. Qiao J, "Histopathological diagnosis of persistent pruritic eruptions associated with adultonset Still’s disease", Histopathology, 74, pp.759~765 (2019)
  3. Maeda-Aoyama N, "Dyskeratotic cells in persistent pruritic skin lesions as a prognostic factor in adult-onset Still disease", Medicine(Baltimore), 99, pp.e19051~ (2020)
  4. Yamaguchi M, "Preliminary criteria for classification of adult Still’s disease", J Rheumatol, 19, pp.424~430 (1992)
  5. Gerfaud-Valentin M, "Adult-onset Still’s disease", Autoimmun Rev, 13, pp.708~722 (2014)
  6. Mahroum N, "Diagnosis and classification of adult Still’s disease", J Autoimmun, 48-49, pp.34~37 (2014)
  7. Kaur S, "Persistent dermal plaque lesions in adult onset Still’s disease", Dermatology, 188, pp.241~242 (1994)
  8. Lübbe J, "Adult-onset Still’s disease with persistent plaques", Br J Dermatol, 141, pp.710~713 (1999)
  9. Sun NZ, "Updates in adult-onset Still disease : atypical cutaneous manifestations and associations with delayed malignancy", J Am Acad Dermatol, 73, pp.294~303 (2015)
  10. Kavusi S, "Atypical eruption but still Still’s : case report and review of the literature", Int J Dermatol, 54, pp.e154~e159 (2015)
  11. Lee JY, "Histopathology of persistent papules and plaques in adult-onset Still’s disease", J Am Acad Dermatol, 52, pp.1003~1008 (2005)
  12. Wolgamot G, "Unique histopathologic findings in a patient with adult-onset Still disease", Am J Dermatopathol, 29, pp.194~196 (2007)
  13. Bresnihan B, "Serum interleukin 18 and interleukin 18 binding protein in rheumatoid arthritis", Ann Rheum Dis, 61, pp.726~729 (2002)

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