[Skip to Content]
[Skip to Content Landing]
Article
April 1986

The Bone Marrow in Urticaria Pigmentosa and Systemic MastocytosisCell Composition and Mast Cell Density in Relation to Urinary Excretion of Tele-methylimidazoleacetic Acid

Author Affiliations

From the Departments of Pathology (Drs Ridell and Enerbäck), Dermatology (Drs Olafsson and Roupe), Clinical Chemistry (Dr Swolin), and Chemical Physiology (Dr Granerus), University of Göteborg, Sahlgrenska Hospital and the Department of Medicine, Östra Hospital, University of Göteborg, Sweden (Dr Rödjer).

Arch Dermatol. 1986;122(4):422-427. doi:10.1001/archderm.1986.01660160078023
Abstract

• The bone marrow sections from five normal subjects and 18 patients with mastocytosis were examined to establish criteria to distinguish urticaria pigmentosa from systemic mastocytosis. Nine patients had increased numbers of mast cells in bone marrow sections stained with a long toluidine blue staining technique specific for mast cells, whereas five patients exhibited increased numbers of mast cells on May-Grünwald-Giemsa-stained smears of bone marrow. A positive correlation between the number of mast cells in sections of the bone marrow and the urinary excretion of the main histamine metabolite tele-methylimidazoleacetic acid was found. In ten of the examined bone marrow specimens, focal lesions containing mast cells, lymphocytes, and eosinophils appeared. The presence of these focal lesions together with either an increased number of mast cells in bone marrow sections and/or increased urinary excretion of tele-methylimidazoleacetic acid is considered diagnostic of systemic mastocytosis. No patient exhibited myeloproliferative condition or other major hematologic abnormality.

(Arch Dermatol 1986;122:422-427)

×