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原发性脾性中性粒细胞减少症——再探讨。

Primary splenic neutropenia--revisited.

作者信息

Hess C E, Jain R K, Ferguson W W

出版信息

South Med J. 1981 Feb;74(2):162-4. doi: 10.1097/00007611-198102000-00009.

Abstract

A patient with acquired, isolated, chronic, severe neutropenia, minimal splenomegaly, and myeloid hyperplasia in the bone marrow is described. Splenectomy resulted in a rise into the normal range of the absolute neutrophil count within 18 hours after ligation of the splenic artery. No other underlying disorders were found, and efforts to demonstrate antineutrophilic autoantibodies before and after splenectomy were unsuccessful. Although this case might be referred to as "primary splenic neutropenia," it is likely that the basic abnormality was intrinsic to the neutrophil. Such cases should be designated "idiopathic neutropenia," since no primary disorder of the spleen can be demonstrated.

摘要

描述了一名患有获得性、孤立性、慢性、严重中性粒细胞减少症、轻度脾肿大且骨髓有髓细胞增生的患者。脾切除术后,在结扎脾动脉后18小时内,绝对中性粒细胞计数升至正常范围。未发现其他潜在疾病,且在脾切除术前和术后检测抗中性粒细胞自身抗体的努力均未成功。尽管该病例可能被称为“原发性脾性中性粒细胞减少症”,但基本异常可能是中性粒细胞本身固有的。由于未发现脾脏的原发性疾病,此类病例应被称为“特发性中性粒细胞减少症”。

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