臨床血液
Online ISSN : 1882-0824
Print ISSN : 0485-1439
ISSN-L : 0485-1439
症例
赤血球貧食を行う反応性組織球増多症を伴い,重症貧血と血小板減少症で発症した早期胃癌合併悪性リンパ腫
中山 志郎石川 隆之矢部 博樹吉田 輝夫永井 謙一内田 博也
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1986 年 27 巻 2 号 p. 202-207

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A 75-year-old male was admitted in November, 1980, for systemic hemorrhage maculae. No superficial lymph node swelling or splenohepatomegaly was observed at admission. Results of blood test were; RBC 310×104/cmm; Hb 9.2 g/dl; Ht 27.9%; reticulocytes 0.6%; WBC 6,800/cmm with almost normal differentials; and PLT 1.4×104/cmm. A bone marrow was of hypercellularity, and megakaryocytes were increased. No pathological cells were observed, but Bormann type I adenocarcinoma was detected at the cardia. Observation of the patient's progress was continued after blood transfusions. Immature lymphocyte-like cells started to develop in the peripheral blood after 15 months, and the patient died of a heavy hemorrhage in the digestive tract that occurred 1 month later. Many thumbnail-sized lymph node swelling mainly in the posterior peritoneum were noted at autopsy. Histological findings were diffusive large cell-type malignant lymphoma with leukemic change. Diffuse and reactive proliferation of histiocytes with erythrophagocytosis were seen in the lymph node, presenting a malignant histiocytosis-like finding. The gastric carcinoma did not extend beyond the muscular layer of the mucosa, and no metastasis to any organ was observed. The proliferation of the histiocytes in this case is presumed to have resulted from stimulation caused in the tissue of the reticuloendothelial system by the gastric carcinoma and to have become a factor for developing hematopenia to a high degree, the occurrence of which is comparatively rare for an initial malignant lymphoma symptom.

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© 1986 日本臨床血液学会
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