リンパ腫の患者における海青組織球

リンパ球性リンパ腫の中年男性は、骨髄、脾腫、血小板減少症に多数の海青組織球を有していました。したがって、彼の病気は、海青組織球の原発症候群の患者の病気を模倣しました。しかし、彼の脾臓における海青組織球の不足、神経疾患の欠如、彼の年齢、および彼の異常な組織球の超微細構造はすべて、後天性症候群の存在の証拠でした。海青色の組織球症の病因と、後天性症例と原発症候群との関係について説明します。

A middle-aged man with lymphocytic lymphoma had numerous sea-blue histiocytes in his bone marrow, splenomegaly and thrombocytopenia. Thus, his illness mimicked that of patients with the primary syndrome of the sea-blue histiocyte. However, the paucity of sea-blue histiocytes in his spleen, the absence of neurologic disease, his age and the ultrastructure of his abnormal histiocytes were all evidence for the presence of the acquired syndrome. The pathogenesis of sea-blue histiocytosis and the relationship between acquired cases and the primary syndrome are discussed.