T. Lehmann et al., SEVERE OSTEOPOROSIS DUE TO SYSTEMIC MAST-CELL DISEASE - SUCCESSFUL TREATMENT WITH INTERFERON-ALPHA-2B, British journal of rheumatology, 35(9), 1996, pp. 898-900
We describe a 33-yr-old man suffering from severe vertebral osteoporos
is and urticaria pigmentosa due to systemic mast cell disease (SMCD).
Because i.v. clodronate therapy could not prevent further vertebral fr
actures, an additional treatment with interferon alpha-2b was initiate
d. During 24 months of treatment, our patient had no further pain epis
odes, no new vertebral fractures were discovered, trabecular bone mine
ral density (BMD) increased significantly and urticarial symptoms impr
oved. Nevertheless, the extent of skin lesions remained unchanged. Oil
histological examination, a remarkable decrease of mast cells was obs
erved in the bone marrow, but not in the skin. Five months after disco
ntinuation of interferon alpha-2b, trabecular BMD decreased and urtica
rial symptoms deteriorated. These findings illustrate a beneficial eff
ect of interferon alpha-2b on SMCD-induced osteoporosis as well as urt
icarial symptoms, and raise the question whether this treatment may ha
ve a diverse impact on mast cell populations in different tissues.