伴有低丙种球蛋白血症和弥散性血管内凝血的组织细胞性髓性网状细胞增生症
Histiocytic medullary reticulosis with hypogammaglobulinaemia and disseminated intravascular coagulation.
作者信息
Clarke P D, Amos R S, Edwards C W, Geddes A M
出版信息
Postgrad Med J. 1977 Jan;53(615):49-50. doi: 10.1136/pgmj.53.615.49.
Abstract
A case of histiocytic medullary reticulosis in a 45-year-old man is described. The presentation with a swinging pyrexia is typical. Associated features were very low levels of all immunoglobulins and proved disseminated intravascular coagulation. Heparin therapy was given and the difficulties of controlling such treatment are demonstrated. It is concluded that an increased awareness of the condition as a cause of pyrexia might lead to an improvement in prognosis.
摘要
本文描述了一名45岁男性组织细胞性髓性网状细胞增多症的病例。以弛张热为表现很典型。相关特征为所有免疫球蛋白水平极低，并证实存在弥散性血管内凝血。给予了肝素治疗，并展示了控制这种治疗的困难。结论是，提高对该病症作为发热原因的认识可能会改善预后。
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本文引用的文献
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Histiocytic medullary reticulosis. Hemolytic anemia due to erythrophagocytosis by histiocytes.组织细胞性髓性网状细胞增生症。由组织细胞吞噬红细胞引起的溶血性贫血。
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Histiocytic medullary reticulosis. The role of phagocytosis in pancytopenia.组织细胞性髓性网状细胞增生症。吞噬作用在全血细胞减少症中的作用。
Arch Intern Med. 1968 Sep;122(3):223-9. doi: 10.1001/archinte.122.3.223.
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A review and reevaluation of the histiocytic disorders.组织细胞增多症的回顾与重新评估
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