N. Haas et al., PHENOTYPIC CHARACTERIZATION OF SKIN-LESIONS IN URTICARIA PIGMENTOSA AND MASTOCYTOMAS, Archives of dermatological research, 287(3-4), 1995, pp. 242-248
In order to identify possible cellular abnormalities in human mastocyt
osis, sections from 13 urticaria pigmentosa lesions and 5 mastocytomas
were compared with 5 normal skin specimens using histochemical, enzym
e histochemical and immunohistochemical techniques. All toluidine blue
-positive mast cells also reacted with Fc epsilon RI and c-kit antibod
ies, almost all stained for tryptase, many for chymase and the myeloid
workshop mast cell antibodies, few for Fc epsilon RII and none for th
e proliferation marker Ki-67. Urticaria pigmentosa lesions contained f
ewer epidermal Langerhans cells and a lower percentage of avidin-posit
ive mast cells than mastocytomas and normal skin. Mastocytomas exhibit
ed generally weaker staining for mast cell markers and mostly lacked F
c epsilon RI-bound IgE on mast cells and Langerhans cells, although th
e receptor was able to bind IgE in tissue sections. Most of the mast c
ell antibodies also reacted with other cell types. Only toluidine blue
, avidin, tryptase and chymase stains were mast cell specific. Mast ce
lls in mastocytosis thus differed only to a minor degree from normal m
ast cells, although distinct pathomechanisms may play a role in urtica
ria pigmentosa and mastocytosis.