مرور Volume 15, Issue 2 بر اساس تاریخ انتشار

در حال نمایش موارد 1 - 6 از 6

  • Goltz syndrome: a case report from Iran 

    Saeid, Pirouzi؛ Fatima, Alikhan؛ Omid, Zargari (Iranian Society of Dermatology, 2012-07-01)
    Focal dermal hypoplasia or Goltz syndrome is a rare genodermatosis involving all three embryonic layers. Herein, the first case of this syndrome from Iran will be reported. The main clinical features were fat herniation, ...

  • Randomized trial of tacrolimus 0.1% ointment versus triamcinolone acetonide 0.1% paste in the treatment of oral pemphigus vulgaris 

    Mohammad-Javad, Nazemi-Tabrizi؛ Parvaneh, Hatami؛ Maryam, Ghiasi؛ Maryam, Daneshpazhooh؛ Cheyda, Chams-Davatchi (Iranian Society of Dermatology, 2012-07-01)
    Background: Pemphigus vulgaris is a rare autoimmune disorder characterized by cutaneous and mucosal blistering. Surprisingly, the management of oral lesions has been detailed only infrequently. As current topical therapies ...

  • High frequency skin ultrasonography in systemic sclerosis 

    Iffat, Hassan؛ Peerzada, Sajad؛ Majid, Jahangir (Iranian Society of Dermatology, 2012-07-01)
    Background: Systemic sclerosis is an autoimmune connective tissue disorder which is characterised by cutaneous and internal organ fibrosis. Raynaud's phenomenon is the earliest feature and may precede the onset of the ...

  • Fine needle aspiration study of the abdominal cutaneous and subcutaneous nodules 

    Shaweta, Rana؛ Nisha, Marwah؛ Promil, Jain؛ Sumiti, Gupta؛ Sanjay, Marwah؛ Rajeev, Sen (Iranian Society of Dermatology, 2012-07-01)
    Background: Abdominal cutaneous and subcutaneous nodules are uncommon benign or malignant lesions. The majority of the malignant nodules are metastatic in origin and may be the initial presentation of a primary malignancy; ...

  • Phakomatosis pigmentovascularis type IIa 

    Abbas, Rasi؛ Mehdi, Tabaie؛ Habib, Hassannejad (Iranian Society of Dermatology, 2012-07-01)
    Phakomatosis Pigmentovascularis (PPV) is a rare cutaneous congenital malformation syndrome, defined as simultaneous occurrence of congenital cutaneous vascular and pigmentary anomalies. As most of the reported cases are ...

  • Successful treatment of major pemphigus vulgaris relapse with mycophenolate mofetil and high-potent topical corticosteroid 

    Nafiseh, Esmaili؛ Cheyda, Chams-Davatchi؛ Maryam, Daneshpazhooh؛ Maryam, Ghiasi؛ Robabe, Abedini؛ Hossein, Mortazavi؛ Iman, Roghani (Iranian Society of Dermatology, 2012-07-01)
    Background: Pemphigus vulgaris (PV) is an autoimmune bullous disorder that is fatal if left untreated. High dose systemic corticosteroids are the basis of therapy. The addition of immunosuppressive agents has improved the ...