All Stories

  1. Two cases of chronic oral ulcers effectively treated with systemic corticosteroid therapy: Circumorificial plasmacytosis and traumatic ulcerative granuloma with stromal eosinophilia
  2. Development of pemphigoid nodularis after remission of bullous lesions
  3. Milia-like idiopathic calcinosis cutis and plaque-type syringoma in a girl with Down syndrome
  4. Possible contribution of autophagy in pyogenic granuloma
  5. Familial acanthosis nigricans with the FGFR3 mutation: Differences of pigmentation between male and female patients
  6. Inhibitory Regulation of Skin Fibrosis in Systemic Sclerosis by Apelin/APJ Signaling
  7. Therapeutic efficacy and adverse events of hydroxychloroquine administration in Japanese systemic/cutaneous lupus erythematosus patients
  8. Cutaneous squamous cell carcinoma, thyroid cancer and Langerhans cell histiocytosis in a patient with X-linked recessive Mendelian susceptibility to mycobacterial diseases with a nuclear factor-κB essential modifier mutation
  9. Dystrophic calcinosis cutis of the auricles after injury in Down's syndrome
  10. Diagnostic criteria, severity classification and guidelines of localized scleroderma
  11. Diagnostic criteria, severity classification and guideline of lichen sclerosus et atrophicus
  12. Guideline for diagnostic criteria, severity classification and treatment of eosinophilic fasciitis
  13. Successful treatment with i.v. immunoglobulin for localized cutaneous immunoglobulin light chain kappa-positive amyloidosis associated with dermatomyositis
  14. Generalized verrucosis caused by various human papillomaviruses in a patient with GATA2 deficiency
  15. Complete resolution of facial molluscum contagiosum in a HIV-infected patient by antiretroviral therapy
  16. Endoplasmic reticulum stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa
  17. Trigeminal trophic syndrome: Analysis of the number of peripheral nerve fibres and blood vessels in the lesional skin
  18. Localized cutaneous immunoglobulin light chain kappa-positive amyloidosis associated with juvenile dermatomyositis
  19. Preface