1977
DOI: 10.1002/1097-0142(197710)40:4<1735::aid-cncr2820400450>3.0.co;2-f
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Acute myelomonocytic leukemia terminating in histiocytic medullary reticulosis.Cytochemical, cytogenetic and electron microscopic studies

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Cited by 34 publications
(3 citation statements)
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“…The simultaneous occurrence of these two aggressive d1sorders is unlikely to be coincidental and raises questi?ns about ~eir relationship. Most of the previously descnbed mahgnant conditions associated with haematophagocytic syndrome were of lymphoid [3][4][5][6][7][8][9][10][11] or haematopoietic [12][13][14] lineage but in few cases mediastinal germ cell tumour [18,19] and carcinoma of va?ous origins have also been reported [17, [19][20][21][22].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The simultaneous occurrence of these two aggressive d1sorders is unlikely to be coincidental and raises questi?ns about ~eir relationship. Most of the previously descnbed mahgnant conditions associated with haematophagocytic syndrome were of lymphoid [3][4][5][6][7][8][9][10][11] or haematopoietic [12][13][14] lineage but in few cases mediastinal germ cell tumour [18,19] and carcinoma of va?ous origins have also been reported [17, [19][20][21][22].…”
Section: Discussionmentioning
confidence: 99%
“…Eur Respir J., 1991, 4, 122-124. Histiocytic medullary reticulosis (HMR) is pathologically characterized by widespread tissue infiltration by atypical histiocytes demonstrating haematophagocytosis [1,2]. Recently an increasing number of HMR has been reported in association with various malignancies mostly of lymphoid [3-ll] or haematopoietic lineage [12][13][14]. Such a haematophagocytic syndrome may include two distinct entities: malignant histiocytosis and a benign (but potentially fatal) reactive histiocytic process mimicking the malignant form.…”
mentioning
confidence: 99%
“…Over the last 15 years there have been reports linking various lymphoreticular malignancies with a malignant histiocytosis-like syndrome (Clark & Dawson 1969, Skarim, Karb & Reynolds 1972, Warnke, Kim & Dorfman 1975, Shreiner 1975, Chen et al 1976, Castoldi et al 1977, Chesney 1977, Lampert, Catovsky & Bergier 1978, Skoog & Feagler 1978, Griffin et al 1978, Karcher, Head & Mullins 1978, Trubowitz, Sobel & David 1980, Starkie 1981. However, with better definition of the cytological features of malignant histiocytosis and description of the virus associated haemophagocytic syndrome (Risdell et al 1979, Manoharan & Catovsky 1981 it has become clear that perhaps the majority of the reported cases are examples of the latter.…”
Section: Introductionmentioning
confidence: 99%