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一例母乳喂养的婴儿出现严重铜缺乏并酷似骨髓增生异常综合征的罕见病例。

A Rare Case of Severe Copper Deficiency in an Infant with Exclusive Breast Feeding Mimicking Myelodysplastic Syndrome.

作者信息

Kohla Samah, Ali Elrazi, Amer Aliaa, Yousif Tayseer, Yassin Mohamed A

机构信息

Department of Laboratory Medicine and Pathology, Hematology Section, Hamad Medical Corporation, Doha, Qatar.

Clinical Pathology Department, Hematology Section, Faculty of Medicine/ Al-Azhar University, Cairo, Egypt.

出版信息

Case Rep Oncol. 2020 Feb 4;13(1):62-68. doi: 10.1159/000505483. eCollection 2020 Jan-Apr.

Abstract

An 11-month-old full-term female infant was referred to the hematology clinic due to marked anemia and neutropenia. She was almost exclusively breastfed and rejecting all trials for supplementary food including artificial formulas. Bone marrow aspirate revealed cytoplasmic vacuolization in precursors of the myeloid and erythroid series with significant dysgranulopoiesis and dyserythropoiesis and ringed sideroblasts. Flow cytometry analysis revealed increased hematogones with aberrant loss/downregulation of CD33 on granulocytes and monocytes (sign of dysmyelopoiesis). Laboratory investigation revealed low serum copper and ceruloplasmin. Administration of a multivitamin including a high concentration of copper for only 1 week improved her hemoglobin and absolute neutrophil count up to 1.9 × 103/µL, then dropped to 0.3 103/µL after she stopped taking the copper multivitamin. Her blood counts improved till total normalization and up to the time this report is issued. The probable role of unrecognized copper deficiency in causing anemia in infants more than 6 months of age is discussed, and the importance of serum copper examination in refractory anemia and neutropenia is emphasized. This case shows that copper deficiency should be an integral part of the differential diagnosis of refractory anemia including sideroblastic anemia and dysplasia. To the best of our knowledge, no such case has previously been described in the literature.

摘要

一名11个月大的足月女婴因明显贫血和中性粒细胞减少被转诊至血液科门诊。她几乎完全母乳喂养,拒绝所有包括人工配方奶粉在内的辅食尝试。骨髓穿刺显示髓系和红系前体细胞出现胞质空泡化,伴有明显的粒细胞生成异常和红细胞生成异常以及环形铁粒幼细胞。流式细胞术分析显示造血细胞增多,粒细胞和单核细胞上CD33异常缺失/下调(骨髓生成异常的迹象)。实验室检查显示血清铜和铜蓝蛋白水平低。给予仅含高浓度铜的多种维生素仅1周后,她的血红蛋白和绝对中性粒细胞计数提高至1.9×10³/µL,但在停止服用含铜多种维生素后降至0.3×10³/µL。直至本报告发布时,她的血细胞计数持续改善直至完全正常。本文讨论了未被认识的铜缺乏在6个月以上婴儿贫血病因中的可能作用,并强调了血清铜检查在难治性贫血和中性粒细胞减少中的重要性。该病例表明,铜缺乏应成为包括铁粒幼细胞贫血和发育异常在内的难治性贫血鉴别诊断的一个组成部分。据我们所知,此前文献中尚未描述过此类病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73f1/7036529/325e6be48d66/cro-0013-0062-g01.jpg

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