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Severe thrombocytosis and anemia associated with celiac disease in a young female patient: a case report

机译:在一名年轻女性患者中与乳糜泻相关的严重血小伤症和贫血症:案例报告

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Introduction Platelet counts exceeding 1.000 × 103/μl are usually considered secondary to another cause, particularly to chronic myeloproliferative disease (CMPD). Reactive thrombocytosis due to iron deficiency rarely exceeds platelet counts of 700 × 103/μl. Case presentation Here we report the case of a young woman presenting with clinical signs of severe anemia. Laboratory findings confirmed an iron-deficiency anemia associated with severe thrombocytosis of 1703 × 103/μl. Macroscopic gastrointestinal and genitourinary tract bleeding was excluded. The excessive elevation of platelets, slightly elevated lactate dehydrogenase and slightly elevated leukocytes along with the absence of other inflammation parameters raised the suspicion of an underlying hematological disease. However, bone marrow evaluation could not prove the suspected diagnosis of a CMPD, especially essential thrombocythemia (ET). In the further clinical course the platelet count returned to normal after raising the hemoglobin to a level close to normal range with erythrocyte transfusion, and normalization of serum iron and decline of erythropoietin. Finally, following small bowel biopsy, despite the absence of typical clinical signs, celiac disease was diagnosed. After discharge from hospital the patient was commenced on a gluten-free diet and her hemoglobin almost completely normalized in the further follow-up period. Conclusion This case illustrates the rare constellation of an extreme thrombocytosis most likely secondary to iron deficiency due to celiac disease. This represents, to the best of the authors' knowledge, the highest reported platelet count coincident with iron deficiency. A potential mechanism for the association of iron-deficiency anemia and thrombocytosis is discussed. Even in the presence of 'atypically' high platelets one should consider the possibility of reactive thrombocytosis. Extreme thrombocytosis could emerge in the case of iron deficiency secondary to celiac disease.
机译:引入超过1.000×103 /μl的血小板计数通常被认为是另一个原因的继发性,特别是慢性野猪植物(CMPD)。由于铁缺乏而导致的反应性血小表积症很少超过700×103 /μl的血小板计数。案例介绍在这里,我们举报了患有严重贫血的临床症状的年轻女性的案例。实验室调查结果证实了缺铁性贫血,其严重的血小伤症为1703×103 /μl。宏观胃肠道和泌尿生殖道出血被排除在外。血小板过度升高,略微升高的乳酸脱氢酶和略微升高的白细胞以及没有其他炎症参数的缺失提高了潜在的血液疾病。然而,骨髓评估不能证明对CMPD的疑似诊断,尤其是必需的血小板(ET)。在进一步的临床过程中,血小板计数在将血红蛋白升高到近常范围内的水平后恢复到正常,以及红细胞输血的正常化,血清铁和促红细胞生成素的序幕。最后,在小肠活检之后,尽管没有典型的临床症状,但乳糜泻被诊断出来。从医院出院后,患者开始在无麸质饮食和她的血红蛋白上几乎完全正常化在进一步的随访期间。结论这种情况说明了由于乳糜泻而导致的最有可能继发于缺铁的极端血小伤症的稀有星座。这代表了据作者所知,最高报告的血小板计数与铁缺乏一致。讨论了缺铁性贫血和血小板增生的潜在机制。即使在“非典型”高血小板存在中,也应考虑反应性血小板菌的可能性。在乳腺疾病中缺铁的情况下,可以出现极端血小板菌。

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