著者
浜中 保三 前田 省吾 赤岩 道夫 岸川 央 沢江 義郎 冨永 喜久男
出版者
一般社団法人 日本血液学会
雑誌
臨床血液 (ISSN:04851439)
巻号頁・発行日
vol.15, no.8, pp.898-903, 1974 (Released:2008-10-31)
参考文献数
8

A 29 years old male patient of Lymphosarcoma with two kinds of M-Components has been described.The patient had been admitted to Shin Kokura Hospital because of lymphadenopathy of cervical, axillar and inguinal area. Biopsy of the cervical lymph node has revealed the histological finding of Lymphosarcoma.During the course of therapy with corticosteroid hormone and cyclophosphamide, two kinds of M-components had appeared in the patient's serum, and had been identified as IgG·κ and IgM·κ by immunoelectrophoresis.Serum concentration of the patient's immunoglobulin had increased three times for IgG and approximately ten times for IgM by antibody agar plate method.In ultracentrifugal analysis, however, there had been no increase of 19S component although 7S component had shown remarkable increase.The dyscrepancy between immunological measurement and ultracentrifugal analysis has been explained by the appearance of IgM with smaller molecular size than usual 19S-IgM. After clinical course of some thirty days the IgM concentration had come down to normal range accompanying the disappearance of monoclonal IgM in immunoelectrophoresis.The mechanism of the appearance of the two kinds of M-components, one of which was transient, has been discussed.
著者
田北 淳 藤永 逸 沢江 義郎 服部 絢一 光安 如成
出版者
一般社団法人 日本血液学会
雑誌
臨床血液 (ISSN:04851439)
巻号頁・発行日
vol.8, no.6, pp.690-698, 1967 (Released:2008-10-20)
参考文献数
33
被引用文献数
3

A 44 years old house-wife was admitted to the hospital in September, 1964, with complaints of general malaise, tachypnea. fever and hemorrhagic diatheses. Physical examinination revealed severe anemia, but neither hepatolienomegaly nor lymphadenopathy. Blood examination showed hemoglobin, 3.8 g/dl, leukocytes, 16,600 with the following differentials: blast cells 74% promyelocytes 1%, metamyelocytes 3%, neutrophils 12%, monocytes 3%, and lymphocytes 17%, and platelets, 76,000. Sternal marrow study showed hypercellularity (261,000) with a good number of myeloblasts (32%).She was treated with blood transfusios of 3,560 ml for 54 days, dexamethasone of 135 mg for 54 days and 6-mercaptopurin 2,050 mg for 35 days, in total, respectively, with an uneventfull effect, and discharged in November, 1964. Thirty days after the discharge, however, leukocyte counts in the blood raised to 29,400 with dominant myeloblasts (85%). She was readmitted in December, 1964. Blood transfusions, dexamethasone and 6-mercaptopurin were administered with no remarkable effect this time.In March, 1965, she complained of back pain for 7 days, followed by untolerable leg pain in about 7 days and then a complete transverse myelitis at the 3rd tholacic segment suddenly developed which comprised paraplegia of the lower extremities, anesthesia in both the abdomen and lower extremities, and retention of urin. She died on 24 th April 1965, about 30 days after the developement of such neurological complications.Post mortem examination disclosed marked infiltration of myeloblasts throughout the tissue, particularly in the bone marrow, spleen, liver and kidneys. Besides, there was found marked myeloblastic infiltration in the dura mater over the whole length of the spinal cord, resulting in liquefaction necrosis of the spinal cord from the 3rd tholacic segments to the cauda equina.