Abstract
A patient is presented who had Castleman's disease with constitutional symptoms, a palpable supraclavicular/axillar mass, and a microcytic anemia, among other laboratory abnormalities, including elevated levels of interleukin-6. Treatment consisted of irradiation of the involved area, with subsequent disappearance of all symptoms and normalization of the laboratory abnormalities. Iron kinetic studies demonstrated a hypoproliferative erythropoiesis, which normalized after radiotherapy. Hypoproliferative erythopoiesis could not be ascribed to serum inhibitors, since normal burst-forming units were observed in the absence or presence of autologous serum. The role of interleukin-6 in relation to Castleman's disease is highlighted.
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Received: 18 December 1995 / Accepted 27 March 1996
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Veldhuis, G., van der Leest, A., de Wolf, J. et al. A case of localized Castleman's disease with systemic involvement: treatment and pathogenetic aspects. Ann Hematol 73, 47–50 (1996). https://doi.org/10.1007/s002770050201
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DOI: https://doi.org/10.1007/s002770050201