1996
DOI: 10.1016/0165-4608(96)00037-4
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A case of acute myelofibrosis with complex karyotypic changes: A type of myelodysplastic syndrome

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Cited by 7 publications
(5 citation statements)
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“…This case highlights the importance of identifying and differentiating APMF from other entities like AML-M7 and RAEB-2 so that aggressive treatment can be instituted. This case also confirms that APMF is a type of AML unlike many who believed it to be a type of MDS 3,4,5,6…”
Section: Discussionsupporting
confidence: 76%
See 1 more Smart Citation
“…This case highlights the importance of identifying and differentiating APMF from other entities like AML-M7 and RAEB-2 so that aggressive treatment can be instituted. This case also confirms that APMF is a type of AML unlike many who believed it to be a type of MDS 3,4,5,6…”
Section: Discussionsupporting
confidence: 76%
“…Though it may be extremely difficult to differentiate APMF from its mimickers in some cases, detailed clinical history and hematological work up can be helpful in such cases. Many consider, as evidenced by many published articles, that APMF is a variant of MDS 3,4,5,6. Since the outcome of these patients is poor therefore it is important to aggressively manage these patients with timely diagnosis as it can reduce morbidity and prolong life.…”
Section: Introductionmentioning
confidence: 99%
“…Cytogenetic features of MDS-F include monosomy 7 [9,16,28]. Complex or other unique cytogenetic features have been reported [7,9,16,[28][29][30][31][32]. Fu, et al [24] studied 266 t-MDS patients and reported that monosomy 5 and monosomy 17 were more commonly detected in t-MDS patients with MF-2/3 (P = 0.031 and P = 0.043, respectively).…”
Section: Genotype Of Primary Mds With Fibrosismentioning
confidence: 99%
“…Cytogenetic features of MDS-F include monosomy 7 [ 9 , 16 , 28 ]. Complex or other unique cytogenetic features have been reported [ 7 , 9 , 16 , 28 - 32 ]. Fu, et al .…”
Section: Introductionmentioning
confidence: 99%
“…47-49 Elizabeth E et al indicated that if MDS is accompanied with fibrosis and chromosomal abnormalities, the prognosis will be poorer than the case MDS is associated with chromosomal abnormalities without fibrosis (Table 1). 50 Therefore, BM biopsy together with cytogenetic study is suggested in MDS patients presenting with a decrease in hematopoietic cell lineages and splenomegaly.…”
Section: Myelofibrosis and Complex Karyotypementioning
confidence: 99%