Abstract
Langerhans cell histiocytosis (LCH) in premature babies is extremely rare as is a vesicular skin rash, while gastrointestinal involvement is associated with a poor outcome. We report a case of LCH in a premature baby presented with isolated vesiculo-papulo-macular skin lesions and insidiously developed gastrointestinal symptoms, haematological and severe pulmonary involvement. We also reviewed a few cases of LCH in premature babies in the English language medical literature. LCH in preterm babies appears to be a severe systemic disease, usually lethal in-utero or post delivery. Conclusion: Careful observation should be applied to newborns with skin-only Langerhans cell histiocytosis in order to identify in time progression to potentially fatal systemic disease.
| Original language | English |
|---|---|
| Pages (from-to) | 1751-1754 |
| Number of pages | 4 |
| Journal | Acta Paediatrica, International Journal of Paediatrics |
| Volume | 97 |
| Issue number | 12 |
| DOIs | |
| State | Published - 1 Dec 2008 |
Keywords
- Gastrointestinal tract
- Langerhans cell histiocytosis
- Premature baby
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health