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为什么骨髓增生异常综合征未被识别和诊断不足?初级保健视角。

Why are myelodysplastic syndromes unrecognized and underdiagnosed? A primary care perspective.

机构信息

Division of Hematology and Oncology, UAB Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama 35294-3300, USA.

出版信息

Am J Med. 2012 Jul;125(7 Suppl):S15-7. doi: 10.1016/j.amjmed.2012.04.017.

Abstract

Primary care physicians (PCPs) may lack a basic understanding of myelodysplastic syndromes (MDS). Two case studies, presented to 44 internal medicine residents and outpatient attending internists, highlighted a potential knowledge gap. A differential diagnosis of MDS was overlooked in a 72-year-old man with several comorbidities and a hemoglobin level of 9.2 g/dL (historical levels, 10.8 to 11.2 g/dL). Despite the acute change in hemoglobin levels, and the presence of comorbid lung and heart disease, there was no immediate recommendation from the PCPs for specialist referral. In contrast, in the second case study a 76-year-old man with a 6-month history of recurrent infections, fatigue, a hemoglobin level of 7.2 g/dL, and multilineage cytopenias typifying the clinical presentation of MDS did receive further attention and workup. With these cases as background, this article examines the potential reasons for the failure of many PCPs to identify MDS, and suggests steps to be taken to improve its diagnosis, early referral, and treatment.

摘要

初级保健医生(PCP)可能对骨髓增生异常综合征(MDS)缺乏基本了解。向 44 名内科住院医师和门诊主治内科医生介绍的两个案例研究突出了潜在的知识差距。一位 72 岁的患有多种合并症和血红蛋白水平为 9.2g/dL(历史水平为 10.8 至 11.2g/dL)的男性被忽视了 MDS 的鉴别诊断。尽管血红蛋白水平急剧变化,并且患有合并的肺部和心脏疾病,但 PCP 并未立即建议转诊给专家。相比之下,在第二个案例研究中,一位 76 岁的男性有 6 个月的反复感染、疲劳、血红蛋白水平为 7.2g/dL 和多系细胞减少症的病史,这些都符合 MDS 的临床表现,因此得到了进一步的关注和检查。本文以这些病例为背景,探讨了许多 PCP 未能识别 MDS 的潜在原因,并提出了改进 MDS 诊断、早期转介和治疗的措施。

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