|
|
つくばリポジトリ (Tulips-R) >
0 コンテンツタイプ別 (Content type) >
01 雑誌発表論文等 (Journal article, etc.) >
Cancer genetics and cytogenetics >
Please use this identifier to cite or link to this item:
http://hdl.handle.net/2241/97858
|
| Title: | Myelodysplastic syndrome accompanied by basophilia and eosinophilia with t(5;12)(q31;p13) |
| Authors: | Katsura, Yukitaka
Suzukawa, Kazumi
Nanmoku, Toru
Nemoto, Noriko
Machino, Takayuki
Obara, Naoshi
Okoshi, Yasushi
Mukai-Yamamoto, Harumi
Hasegawa, Yuichi
Kojima, Hiroshi
Kawakami, Yasushi
Nagasawa, Toshiro
鈴川, 和己 |
| Issue Date: | Oct-2007 |
| Publisher: | Elsevier Inc. |
| Journal Title: | Cancer Genetics and Cytogenetics |
| Volume: | 178 |
| Issue: | 1 |
| Start Page: | 85 |
| End Page: | 88 |
| DOI: | 10.1016/j.cancergencyto.2007.05.020 |
| PMID: | 17889716 |
| Abstract: | The t(5;12)(q31not, vert, similar35;p12not, vert, similar13) is rare among cytogenetically categorized myeloid diseases. Here we describe a case of myelodysplastic syndrome (MDS) with basophilia followed by leukocytosis, basophilia, and eosinophilia with t(5;12)(q31;p13).
A 44-year-old man was referred to Tsukuba University Hospital in August 2005, due to severe anemia and thrombocytopenia. Peripheral blood examination showed hemoglobin 4.5 g/dL, with mean corpuscular volume 109 fL, platelets 73 × 109/L, and white blood cells 4.9 × 109/L with 23% basophils, 3% eosinophils, and 0% blasts. Bone marrow was slightly hypocellular, with trilineage dysplasia. Cytogenetic examination of the bone marrow cells revealed a normal karyotype, 46,XY. A diagnosis of myelodysplastic syndrome–refractory anemia with excess blasts type 2 (MDS-RAEB2) was made according to the WHO classification. |
| URI: | http://hdl.handle.net/2241/97858 |
| Rights: | ©2007 Elsevier Inc. |
| Text Version: | author |
| Appears in Collections: | Cancer genetics and cytogenetics
鈴川 和己 (Suzukawa Kazumi)
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|
