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约克血小板综合征:第四例具有不同寻常病理特征的病例。

The York platelet syndrome: a fourth case with unusual pathologic features.

机构信息

Department of Laboratory Medicine, Pathology and Pediatrics, University of Minnesota School of Medicine, Minneapolis, MN, USA.

出版信息

Platelets. 2013;24(1):44-50. doi: 10.3109/09537104.2012.658527. Epub 2012 Jul 3.

Abstract

The present report describes a fourth patient with platelet pathological features identical to those found in the first three cases with the York platelet syndrome (YPS), as well as other findings that suggest he may be a variant. His platelets contain the same giant opaque and target organelles found earlier, as well as enlarged organelles with a gray appearing matrix. It is possible that the giant structures have the same source, but are at different stages of development. The fourth patient has platelet pathology suggestive of other thrombocyte disorders. He has many large platelets and normal sized thrombocytes nearly devoid of alpha granules. As a result, he was originally thought to have the gray platelet syndrome. He also has significant numbers of platelets attached to platelets and platelets in platelets as seen in patients with the X-linked GATA-1 mutation. Some of the fourth YPS patient's platelets contained massive alpha granules suggesting the possibility of the Paris Trousseau Jacobson Syndrome. Yet, none of these other platelet disorders had giant dense organelles like those found in YPS thrombocytes. As a result, it is reasonable to include this child with the other three, and diagnose him as a patient with the YPS.

摘要

本报告描述了第四例血小板病理特征与前三例约克血小板综合征(YPS)患者完全相同的患者,以及其他一些表明他可能是一种变体的发现。他的血小板含有与早期发现的相同的巨大不透明和靶细胞器,以及具有灰色基质的增大细胞器。这些巨大结构可能具有相同的来源,但处于不同的发育阶段。第四例患者的血小板病理学表现提示存在其他血小板疾病。他有许多大型血小板和正常大小的几乎没有α颗粒的血小板。因此,他最初被认为患有灰色血小板综合征。他还存在大量附着在血小板上的血小板和血小板中的血小板,如 X 连锁 GATA-1 突变患者所见。第四例 YPS 患者的一些血小板含有巨大的α颗粒,提示可能存在巴黎特鲁索·雅各布森综合征。然而,这些其他血小板疾病均没有 YPS 血小板中发现的巨大致密细胞器。因此,将这个孩子与其他三个孩子一起归入 YPS 患者并进行诊断是合理的。

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