Source:http://linkedlifedata.com/resource/pubmed/id/19955712
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2009-12-17
|
pubmed:abstractText |
Secondary pulmonary alveolar proteinosis (PAP) is a rare lung disease that has been reported in 13 cases of myelodysplastic syndromes (MDS). A dicentric isochromosome of deleted chromosome 20q, idic(20q-), is a newly recognized rare, but recurrent, cytogenetic anomaly that has been described in 28 cases of MDS. Recently, we encountered an interesting MDS patient with idic(20q-) and secondary PAP. At presentation, she was a 40-year-old woman with pancytopenia and dysplasia involving 2 cell lineages that were compatible with refractory cytopenia with multilineage dysplasia. A chromosome analysis of bone marrow cells using the R-banding technique revealed a karyotype of 46,XX,-20 and +a small metacentric marker chromosome. Fluorescence in situ hybridization demonstrated this marker chromosome to be idic(20q-). Three years after presentation, her disease was complicated by secondary PAP that was confirmed by chest computed tomographic scans and a thoracoscopic lung biopsy, revealing the characteristic periodic acid Schiff stain-positive materials filling the alveoli. The patient subsequently died of respiratory failure 45 months after diagnosis. To our knowledge, this is the first MDS patient with idic(20q-) and secondary PAP to be reported in the literature. Moreover, this patient is also the 29th MDS case with idic(20q-).
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
1421-9662
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2009 S. Karger AG, Basel.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
123
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
55-8
|
pubmed:meshHeading |
pubmed-meshheading:19955712-Adult,
pubmed-meshheading:19955712-Chromosomes, Human, Pair 20,
pubmed-meshheading:19955712-Fatal Outcome,
pubmed-meshheading:19955712-Female,
pubmed-meshheading:19955712-Humans,
pubmed-meshheading:19955712-In Situ Hybridization, Fluorescence,
pubmed-meshheading:19955712-Isochromosomes,
pubmed-meshheading:19955712-Myelodysplastic Syndromes,
pubmed-meshheading:19955712-Pulmonary Alveolar Proteinosis
|
pubmed:year |
2010
|
pubmed:articleTitle |
Pulmonary alveolar proteinosis as a terminal complication in a case of myelodysplastic syndrome with idic(20q-).
|
pubmed:affiliation |
Key Laboratory of Thrombosis and Hemostasis, Jiangsu Institute of Hematology, First Affiliated Hospital of Soochow University, 188 Shizi Street, Suzhou, PR China. chromosome8471@yahoo.com.cn
|
pubmed:publicationType |
Journal Article,
Case Reports
|