 | Your DermAtlas query returned 6 ImagesClick on the IMAGE to see an enlargement. |
 © 2001-2009, DermAtlas | Image Name: | perioraldermatitis_1_011113 | File Type: | jpg | |
| Diagnosis: | DERMATITIS, LIP LICKER'S / DERMATITIS, CONTACT IRRITANT / DERMATITIS, PERIORAL | Category: | papulosquamous eruptions / factitial / self Induced disorders / psychodermatosis | ||
| Body Site: | chin / lip | Age: | 11 years | ||
| Contributor: | Kerry Bron, MD | ||||
| Description: | This eleven-year old boy had persistent lip-licking behavior. This dermatitis had been present for four months and was not responding to treatment with antibiotics (erythromycin) and emollients (petrolatum). He had no other medical problems, and the inside of his mouth was clear. | ||||
| Comments: | This eleven-year old boy with a history of chronic liplicking developed asymptomatic perioral dermatitis.The rash persisted for 4 months despite treatment with topical erythromycin and petrolatum. He was well, and the remainder of his physical examination including his mouth was normal. | ||||
 © 2001-2009, DermAtlas | Image Name: | epidermolysisbullosa_4_011113 | File Type: | jpg | |
| Diagnosis: | EPIDERMOLYSIS BULLOSA, DERMOLYTIC (DYSTROPHIC) | Category: | vesiculobullous eruptions, mechanobullous | ||
| Body Site: | thigh | Age: | 11 months | ||
| Contributor: | Kerry Bron, MD | ||||
| Description: | A healing erosion on the left lower extremity of this 11 month old female who has had blistering since birth. | ||||
| Comments: | A healthy 11 month old girl with autosomal dominant dermolytic epidermolysis bullosa developed recurrent blisters on her extremities with the most prominent lesions on her hands and feet. | ||||
| Related Images: | All related Images epidermolysisbullosa_2_011113 epidermolysisbullosa_3_011113 | ||||
 © 2001-2009, DermAtlas | Image Name: | epidermolysisbullosa_3_011113 | File Type: | jpg | |
| Diagnosis: | EPIDERMOLYSIS BULLOSA, DERMOLYTIC (DYSTROPHIC) | Category: | vesiculobullous eruptions, mechanobullous / genodermatosis/genetic disorder / neonatal dermatology | ||
| Body Site: | leg / hand | Age: | 11 months | ||
| Contributor: | Kerry Bron, MD | ||||
| Description: | crusted vesicles and erosions | ||||
| Comments: | A healthy 11 month old girl with autosomal dominant dermolytic epidermolysis bullosa developed recurrent blisters on her extremities with the most prominent lesions on her hands and feet. Note the milia on the top of her hand and associated nail dystrophy. | ||||
| Related Images: | All related Images epidermolysisbullosa_2_011113 epidermolysisbullosa_4_011113 | ||||
 © 2001-2009, DermAtlas | Image Name: | epidermolysisbullosa_2_011113 | File Type: | jpg | |
| Diagnosis: | EPIDERMOLYSIS BULLOSA, DERMOLYTIC (DYSTROPHIC) | Category: | vesiculobullous eruptions, mechanobullous / genodermatosis/genetic disorder / neonatal dermatology | ||
| Body Site: | hand / finger nail, hand | Age: | 11 months | ||
| Contributor: | Kerry Bron, MD | ||||
| Description: | healing erosions, milia, and nail dystrophy | ||||
| Comments: | At birth a healthy 11 month old girl with autosomal dominant dermolytic epidermolysis bullosa developed recurrent blisters on her extremities with the most prominent lesions on her hands and feet. Note the milia on the top of her hand and associated nail dystrophy. | ||||
| Related Images: | All related Images epidermolysisbullosa_3_011113 epidermolysisbullosa_4_011113 | ||||
 © 2001-2009, DermAtlas | Image Name: | leopardsyndrome_1_010907 | File Type: | jpg | |
| Diagnosis: | LEOPARD SYNDROME / MULTIPLE LENTIGINES SYNDROME / LENTIGO | Category: | genodermatosis/genetic disorder / hyperpigmentation | ||
| Body Site: | chest / trunk | Age: | 12 years | ||
| Contributor: | Kerry Bron, MD | ||||
| Description: | multiple disseminated hyperpigmented 2-5 mm macules | ||||
| Comments: | This 12 year old boy with multiple lentigines also had pulmonic stenosis, developmental delay, and undescended testicles, findings associated with L(entigines), E(KG abnormalities), O(cular hypertelorism), P(ulmonic stenosis), A(bmormal genitalia, R(etardation of growth), D(eafness, neurosensory) syndrome. His sister and father had similar skin findings consistent with autosomal dominant inheritance. | ||||
 © 2001-2009, DermAtlas | Image Name: | lamellarichthyosis_1_010906 | File Type: | jpg | |
| Diagnosis: | ICHTHYOSIS, LAMELLAR | Category: | papulosquamous eruptions / genodermatosis/genetic disorder / neonatal dermatology | ||
| Body Site: | trunk / chest abdomen | Age: | 12 years | ||
| Contributor: | Kerry Bron, MD | ||||
| Description: | thick confluent hyperpigmented plate like scale | ||||
| Comments: | This 12 year old boy developed chronic thick hyperpigmented platelike scales typical of lamellar ichthyosis after the collodion membrane present at birth desquamated during the newborn period | ||||
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