灰血小板综合征与妊娠:病例报告及文献复习

Francisco Ibarguengoitia-Ochoa, C. M. Sepúlveda-Rivera, Sergio Emmanuel Santoyo-Rosas, Diego Arturo Gonzalez-Vazquez, Jessica Aidee Mora-Galvan, Samuel Vargas-Trujillo
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引用次数: 0

摘要

灰色血小板综合征是一种罕见的遗传性血小板疾病,其特征是血小板减少和血小板功能障碍,特异性缺乏α颗粒。电子显微镜是一种快速的诊断方法。我们提出围产期结果的诊断为灰色血小板综合征的病人。我们回顾了一例患者灰色血小板综合征在研究所国家围产。她今年26岁,怀孕21周。初步实验室发现血小板64000 /mm 3,怀疑为灰色血小板综合征,行外周血涂片示血小板苍白,电镜检查证实为血小板α颗粒缺失。妊娠38.4周剖宫产1例女婴,体重2588 g,出生时血小板计数为119000 /mm 3。灰色血小板综合征患者的治疗尚无普遍共识,管理必须是产科、血液学和麻醉学服务之间的多学科合作。临床妇产科杂志,2019;8(2):54-56 doi: https://doi.org/10.14740/jcgo555
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Grey Platelet Syndrome and Pregnancy: A Case Report and Literature Review
Grey platelet syndrome is an uncommon hereditary platelet disorder, and is characterized by thrombocytopenia and platelet dysfunction with a specific absence of alpha-granules. Electronic microscopy is a quick test that can confirm the diagnosis. We present perinatal results of a patient with diagnosed grey platelet syndrome. We reviewed the case of a patient with grey platelet syndrome at Instituto Nacional de Perinatologia. She is 26 years old, with 21 weeks’ gestation. It is noted in initial laboratories a platelet amount of 64,000/mm 3 , and grey platelet syndrome is suspected, so peripheral blood smear is carried out which showed pale platelets, and electronic microscopy was performed to confirm the disorder, which showed the absence of platelet alpha-granules. A female newborn was delivered at 38.4 week of gestation by abdominal cesarean section, weighing 2,588 g, with platelet count at birth of 119,000/mm 3 . There is no general consensus of treatment in patients with grey platelet syndrome, and management must be multi-disciplinary between obstetrics, hematology and anesthesiology services. J Clin Gynecol Obstet. 2019;8(2):54-56 doi: https://doi.org/10.14740/jcgo555
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