Journal of Clinical and Experimental Hematopathology
Online ISSN : 1880-9952
Print ISSN : 1346-4280
ISSN-L : 1346-4280
Case Study
Successful Surgical Treatment for Pulmonary Crystal-Storing Histiocytosis Following the Onset of Gastric Non-Hodgkin Lymphoma
Noriaki KawanoKiichiro BeppuMayumi OyamaDaisuke HimejiShuro YoshidaTakuro KuriyamaNobuyuki OnoHiroyuki MasuyamaKiyoshi YamashitaKenichiro YamaguchiYoshiya ShimaoKoichi OshimaYuji UedaAkira Ueda
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2013 Volume 53 Issue 3 Pages 241-245

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Abstract

Crystal-storing histiocytosis is a rare clinical entity characterized by an increase in the number of abnormal histiocytes accompanied by accumulation of crystallized immunoglobulins. We describe the case of an 80-year-old man who presented with crystal-storing histiocytosis of the lung 13 years after receiving a diagnosis of gastric non-Hodgkin lymphoma (NHL ; clinical stage, Lugano IA). After wedge resection of the left upper lobe, the histological findings showed crystal-storing histiocytosis with CD68+, some small to medium lymphoid cells with CD79a+ with κ+(weekly) and λ-, and some plasma cells with CD138+, and rearrangement of the immunoglobulin heavy chain. Based on the nonrecurrent gastric NHL, small B-cell population, and failure to detect the same clone by polymerase chain reaction analysis, our case was classified as pulmonary localized crystal-storing histiocytosis without underlying lymphoproliferative or plasma cell disorder. The findings of minor B-cell populations harboring a heavy chain rearrangement with slight light-chain restriction (κ > λ) may be related to the pathogenesis of crystallogenesis and crystal-storing histiocytosis. Moreover, surgical treatment may be an effective therapeutic option for solitary crystal-storing histiocytosis. [J Clin Exp Hematop 53(3) : 241-245, 2013]

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© 2013 by The Japanese Society for Lymphoreticular Tissue Research
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