Differential diagnosis of hypomelanoses in children (N. Van Geel (Ghent, Belgium))
Use a stepwise approach:
1. Step 1 History
- -congenital or acquired
- -stable or progressive
- -other medical problems
- -family history
2. Step 2 Clinical Examination
- -localisation (Woods light important especially in the localized form)
- -number of lesions
- -pattern (linear blaschkoid, segmental)
- -hypomelanosis or amelanosis
- -other problems (neurological, eyes)
3. Step 3: Apply information of flowchart (differential diagnosis)
- -if diffuse: presence or absence of ocular involvmenet
- a. ocular involvement: albinos group, also Griscelli syndrome, Chediak-Higashi syndrome
- b. no ocular involvement: think of Metabolic causes: Menkies syndrome, phenylcetonuria
- if localized
- -depigmentation: waardenburg, piedbaldism
- -hypopigmentation: tuberous scleroris, nevus depigmentosus, Pigmentation of inflammatory (PIH) or infectious origin, Pigmentary mosaicism (Hypomelanosis of Ito) lichen striatus
- -no pigment disorder: nevus anemicus
Ash-leaf macule in Tuberous Sclerosis
Source of Information: Sy 17. Pigmentation Disorders: From Vitiligo to Hyyperpigmentation. 2011 (10) – 20th Annual Congress of the EADV (European Academy of Dermatology and Venerology) – Lisbon (Lisboa), Portugal