Multiple autoimmune haemopoietic disorders and insidious clonal proliferation of large granular lymphocytes

We report a patient with clonal proliferation of CD3+8+TCRαβ+ large granular lymphocytes (LGL) presenting multiple episodes of autoimmune cytopenia, including autoimmune neutropenia, idiopathic thrombocytopenic purpura, autoimmune haemolytic anaemia, and pure red cell aplasia. Each disorder appeared...

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Veröffentlicht in:British journal of haematology 1999-12, Vol.107 (3), p.670-673
Hauptverfasser: Akashi, Koichi, Shibuya, Tsunefumi, Taniguchi, Shuichi, Hayashi, Shin, Iwasaki, Hiromi, Teshima, Takanori, Takamatsu, Yasushi, Gondo, Hisashi, Okamura, Takashi, Harada, Mine, Niho, Yoshiyuki
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Sprache:eng
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Zusammenfassung:We report a patient with clonal proliferation of CD3+8+TCRαβ+ large granular lymphocytes (LGL) presenting multiple episodes of autoimmune cytopenia, including autoimmune neutropenia, idiopathic thrombocytopenic purpura, autoimmune haemolytic anaemia, and pure red cell aplasia. Each disorder appeared separately or as a combination during an 11‐year clinical course. The increase of blood CD3+8+TCRαβ+ LGL was detected 6 years after the initial diagnosis of cytopenia, but the absolute number of LGL cells was always
ISSN:0007-1048
1365-2141
DOI:10.1046/j.1365-2141.1999.01734.x