一例儿童无症状原发性血小板增多症病例。
A Case of Asymptomatic Essential Thrombocythemia in a Child.
作者信息
Aljuaid Mohammed, Alahmadi Ziad, Alasmari Badriah, Alyamani Arwa, Khan Eman
机构信息
Paediatrics, Royal Commission Hospital, Yanbu, SAU.
Internal Medicine, Umm Al-Qura University, Makkah, SAU.
出版信息
Cureus. 2022 Aug 26;14(8):e28455. doi: 10.7759/cureus.28455. eCollection 2022 Aug.
Various factors can be linked to an increase in platelet count. Yet thrombocytosis could be essential. Many genetic mutations have been associated with essential thrombocytosis, which also increases the possibility of myelofibrotic transformation. In pediatrics, essential thrombocytosis is not well-studied. In this article, we present a rare case of a 42-month-old male patient who presented with essential thrombocytosis associated with myeloproliferative leukemia (MPL) gene mutation.
多种因素可能与血小板计数增加有关。然而，血小板增多症可能至关重要。许多基因突变与原发性血小板增多症有关，这也增加了骨髓纤维化转化的可能性。在儿科，原发性血小板增多症的研究并不充分。在本文中，我们报告了一例罕见病例，一名42个月大的男性患者患有与骨髓增殖性白血病（MPL）基因突变相关的原发性血小板增多症。
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