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遗传性巨大血小板综合征患者血涂片及悬浮状态下血小板的大小和形态:两种异常类型的证据

Platelet size and shape in hereditary giant platelet syndromes on blood smear and in suspension: evidence for two types of abnormalities.

作者信息

Milton J G, Hutton R A, Tuddenham E G, Frojmovic M M

出版信息

J Lab Clin Med. 1985 Sep;106(3):326-35.

PMID:4031633
Abstract

Platelet size on blood smear is compared with platelet size and shape in suspension (i.e., whole blood and citrated platelet-rich plasma [PRP]) for normal donors and 16 patients with hereditary "giant" platelet syndromes (HGPS), including Bernard-Soulier syndrome (BSS) (seven patients), Montreal platelet syndrome (MPS) (three patients), May-Hegglin anomaly (one patient) and Rafael platelet defect (one patient). In whole blood platelet shape is normal for HGPS, but in PRP for 10 of 16 patients with HGPS there is a decrease in the proportion of smooth, discoid-shaped platelets (discocytes [D]). The platelets of all patients with HGPS had abnormally large mean volume (VT) and increased size on peripheral blood smear. Furthermore, 12 of 16 patients with HGPS, including six of seven donors with BSS, had abnormally large discocytes. The measured size of HGPS shape-changed platelets was compared with the size predicted from the size of the D by assuming that the relationship between the size of shape-changed platelets and D was the same as observed for normal donors. In this manner it was shown that for all donors with BSS and MPS, the shape-changed platelets are disproportionately larger than the D. In contrast, in the remaining patients with HGPS the size of the shape-changed platelets was consistent with the size predicted from the D. Examination of VT for MPS as a function of time after addition of 10 mumol/L adenosine diphosphate to PRP revealed an abnormal time course, thereby pointing to an abnormality in the mechanisms that regulate platelet size during shape change. With the lone exceptions of BSS and MPS, the size of platelets on blood smear was well correlated with the total platelet plasma membrane surface area as measured by the osmotic spherocyte method. Our observations point to two distinct abnormalities in platelet size in HGPS: a disproportion between the size of D and "shape-changed" platelets, which may be related to an abnormal shape change and which is observed only for MPS and BSS, and an abnormal increase in platelet size on blood smear, which appears to reflect the increased amount of platelet plasma membrane in other HGPS platelets.

摘要

将正常献血者以及16例遗传性“巨大”血小板综合征(HGPS)患者(包括7例伯纳德-索利尔综合征(BSS)患者、3例蒙特利尔血小板综合征(MPS)患者、1例梅-赫格琳异常患者和1例拉斐尔血小板缺陷患者)血涂片上的血小板大小与悬浮液(即全血和枸橼酸化富血小板血浆[PRP])中的血小板大小和形状进行比较。在全血中,HGPS患者的血小板形状正常,但在PRP中,16例HGPS患者中有10例的光滑盘状血小板(双凹圆盘形细胞[D])比例降低。所有HGPS患者的血小板平均体积(VT)均异常增大,在外周血涂片上尺寸也增大。此外,16例HGPS患者中有12例,包括7例BSS患者中的6例,有异常大的双凹圆盘形细胞。将HGPS形状改变的血小板的测量尺寸与通过假设形状改变的血小板与D的大小关系与正常献血者观察到的相同,从D的大小预测的尺寸进行比较。通过这种方式表明,对于所有BSS和MPS患者,形状改变的血小板比D不成比例地更大。相反,在其余HGPS患者中,形状改变的血小板大小与从D预测的大小一致。向PRP中加入10μmol/L二磷酸腺苷后,对MPS患者的VT随时间变化进行检查,发现其时间进程异常,从而表明在形状改变过程中调节血小板大小的机制存在异常。除了BSS和MPS这两个唯一的例外,血涂片上血小板的大小与通过渗透球形红细胞法测量的血小板总质膜表面积密切相关。我们的观察结果指出了HGPS患者血小板大小存在两种不同的异常情况:D与“形状改变”血小板大小之间的不成比例,这可能与异常的形状改变有关,且仅在MPS和BSS中观察到;血涂片上血小板大小的异常增加,这似乎反映了其他HGPS血小板中血小板质膜数量的增加。

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