1  and chymase by mast cells of a patient with urticaria pigmentosa and aggressive systemic mastocytosi

2                                              Urticaria pigmentosa and mast cell mediator release symp

3 cell infiltration-related symptoms including urticaria pigmentosa and organomegaly (P < .02).

4 differed significantly between patients with urticaria pigmentosa and those with diffuse cutaneous (P

5 gen C-telopeptide, hip bone mineral density, urticaria pigmentosa, and alcohol intake are easy to col

6 e), low hip bone mineral density, absence of urticaria pigmentosa, and alcohol intake at the time of

7 phylaxis, documented hypotension, absence of urticaria pigmentosa, and normal SBT levels.

8 ween patients with and without osteoporosis, urticaria pigmentosa or anaphylaxis, respectively (P < 0

9 thic" anaphylaxis who did not exhibit either urticaria pigmentosa or the characteristic bone marrow b

10 the typical maculopapular cutaneous lesions (urticaria pigmentosa) should be subdivided into 2 varian

11 idermal melanin, a clinical picture known as urticaria pigmentosa (UP).

12 on of ISM without accompanying skin lesions [urticaria pigmentosa (UP)] are lacking.

13 mL) were as follows: controls, 176 (n = 60); urticaria pigmentosa without systemic involvement, 194 (