Case Report
Iatrogenic Anetoderma of Prematurity: A Case Report and Review of the Literature
Table 1
Classification of anetoderma [
5,
6].
(a) Primary anetoderma (idiopathic) |
| Jadassohn-Pellizzari type (precedent clinical inflammation) | | Schweninger-Buzzi type (no precedent clinical inflammation) | | Familial | | Congenital | |
|
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(b) Secondary anetoderma (diseases associated with anetoderma) |
| (1) Autoimmune conditions | (i) Addison disease (ii) Antiphospholipid syndrome (iii) Discoid lupus (iv) Graves disease (v) Haemolytic anemia (vi) Sjögren syndrome (vii) Systemic lupus erythematosus (viii) Takayasu arteritis |
| (2) Infectious conditions | (i) Chicken pox (ii) HIV infection (iii) Leprosy (iv) Lyme disease (v) Molluscum contagiosum (vi) Syphilis (vii) Tuberculosis |
| (3) Inflammatory conditions | (i) Acne vulgaris (ii) Granuloma annulare (iii) Insect bites (iv) Mastocytosis (v) Prurigo nodularis |
| (4) Tumor/deposition conditions (benign and malignant) | (i) Cutaneous plasmacytoma (ii) Lymphocytoma cutis (iii) Melanocytic naevi (iv) Myxofibrosarcoma (v) Nodular amyloidosis (vi) Pilomatricomas (vii) Schwannomas (viii) Xanthomas |
| (5) Drug induced | (i) Penicillamine (ii) Hepatitis B vaccination |
| (6) Iatrogenic | Anetoderma of prematurity |
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