急性淋巴细胞白血病的青春期女孩与格雷夫斯病:巧合或后果

G. F. Fadlalbari, Samar S. Hassan, A. Abdalla, Samar Omer Abusamra, Abeer Mohamed Abdalrhman, M. A. Abdullah
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引用次数: 0

摘要

背景:Graves病(GD)相关的骨髓损伤通常表现为粒细胞缺乏症或全血细胞减少症。然而,急性淋巴细胞白血病(ALL)已报道最近在一个成年患者GD。其潜在的发病机制尚不完全清楚。然而,抗甲状腺药物的有害作用或对骨髓细胞的自身免疫反应预计是致病因素。病例介绍:我们报告了一位16.5岁的GD女孩,她在发病的前14个月服用了卡咪唑,随访不规律;后来因为她得了甲状腺功能减退症而停药了。与此同时,她出现了严重的贫血,没有发烧,需要输血。8个月后,患者出现甲状腺毒症复发、发热性疾病、骨痛、全血细胞减少症,骨髓检查证实为ALL。结论:年轻GD患者出现ALL是前所未有的。虽然很难证明它们之间的因果关系,但不能否认需要进一步研究。
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Acute Lymphoblastic Leukemia in an Adolescent Girl with Graves’ Disease: A Coincidence or Consequence
Background: Graves’ disease (GD)-related bone marrow injury presents usually as agranulocytosis or less commonly as pancytopenia. However, acute lymphoblastic leukemia (ALL) has been reported recently in an adult patient with GD. The underlying pathogenesis is not fully understood. Nevertheless, the harmful effects of anti-thyroid drugs or autoimmune reaction to bone marrow cells are anticipated to be the causative factors. Case Presentation: We report a 16.5-year-old girl with GD who was on carbimazole for the first 14 months of her illness, with irregular follow-up; then it was withdrawn because she developed hypothyroidism. Meanwhile, she developed severe anemia without fever which necessitated blood transfusion. Eight months later, she presented with thyrotoxicosis relapse, febrile illness, bone pain, and pancytopenia which was proved to be ALL on bone marrow examination. Conclusion: The presence of ALL in a young GD patient is an unprecedented event. Although it is difficult to demonstrate the causality between them, need for further studies cannot be denied.
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