Neonatal mastocytosis with pachydermic bullous skin without c-Kit 816 mutation

Dermatology. 2006;212(1):70-2. doi: 10.1159/000089026.

Abstract

Background: Bullous mastocytosis is an unusual variant of mast cell disease with widespread bullae as the main cutaneous feature induced by mast cell proteases that cause dermoepidermal separation.

Case report: A rare case of diffuse cutaneous bullous mastocytosis with pachydermia and unusually extensive skin folding is described in a 3-week-old girl. The diagnosis was confirmed by immunohistochemistry with Giemsa stain, the naphthol ASD chloroacetate esterase reaction and elevated blood levels for tryptase, histamine in serum and histamine and 1.4-methylimidazol acetic acid in the 24-hour urine. Blood cell count was normal, as were thrombocytosis and leukocytosis. FACS analysis of the bone marrow aspiration material showed 1% mast cells. No c-Kit 816 [Asp-->Val] somatic mutation was found. Systemic involvement of other organs was excluded.

Discussion: The prognosis of c-Kit-negative diffuse bullous mastocytosis is not known. Regular blood controls are mandatory, and screening for germ cell ovarian cancer and bone marrow controls should be performed as well.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Humans
  • Infant, Newborn
  • Mutation, Missense
  • Proto-Oncogene Proteins c-kit / genetics
  • Skin / metabolism
  • Skin / pathology*
  • Urticaria Pigmentosa / genetics
  • Urticaria Pigmentosa / pathology*

Substances

  • Proto-Oncogene Proteins c-kit