Journal of Okayama Medical Association
Published by Okayama Medical Association

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Full-text articles are available 3 years after publication.

脾腫・白血球増多症を主徴とし診断に著しく困難を感じた伝染性単核症の一例

Kondo, Tadasuke
Oguchi, Kiyoshi
Yamamoto, Hiroshi
Goto, Shoichiro
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Abstract
Three years ago the patient was pointed out splenomegaly and leukocytosis associated with no swelling of lymphatic glands after pneumonia, but had no complains till admission's time. Leukocytosis was always counted over 10000, and was occupied indifinite large lymphcytes identified as Downey Ⅱ type cell at 55.6% in maximum of its classification. Bone marrow, red blood cell, reticulocyte and platelets count were normal. Spleenbiopsy showed a full of atypical lymphcytes without leucaemic infiltration in spleen. The infiltration of same atypical lymphcytes with intensely degenerated nature were found by liverbiopsy, and these cells had not any tendency to increase in the liver. Axillary lymphatic gland extirpasion's tissue picture coincided with chronic lymphadenitis, and extensive reticulo-and sinusendotheliar cell increasing were also seen. Several serologic reactions, i.e. Paul-Bunnel reation, Weil-Felix reaction and Davidson's adosorption test had little value to making diagnosis.
ISSN
0030-1558
NCID
AN00032489