Progressive nodular histiocytosis.

Olaf Hilker, Alexander Kovneristy, Rita Varga, Thorsten Neubert, Ulrich Wesselmann, Michael J Flaig, Thomas Ruzicka, Walter Burgdorf, Percy Lehmann

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2013;11(4):301-7

PMID: 23231636

Abstract

Progressive nodular histiocytosis (PNH) represents a very rare type of non-Langerhans cell histiocytosis (NLCH). It can be distinguished from other types by the occurrence of yellow to red-brown papules and nodules measuring a few centimeters in size. Histologically the nodules represent spindle-cell xanthogranulomas. We report on two new cases of PNH with novel clinical symptoms. In the first case, the patient had microcytic anemia due to massive iron deposition in the nodules and a progressively worsening limp due to involvement of the soles. The complex therapeutic challenge was effectively managed by successive surgical ablation of all visible lesions. The second patient had epibulbar infiltrates. The clinical variability of PNH leads to considerable overlap with other forms of NLCH.

© The Authors • Journal compilation © Blackwell Verlag GmbH, Berlin.

Address: Helios Klinikum Wuppertal, Department of Dermatology, Allergology, and Surgical Dermatology, Wuppertal, Germany. [email protected]
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