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[红细胞大细胞症的血液学意义:对109例连续研究病例的前瞻性分析]

[Hematologic significance of erythrocytic macrocytosis: prospective analysis of 109 successively studied cases].

作者信息

Outeiriño Pérez J J, Sánchez Fayos J, Outeiriño Hernanz J, Calabuig T, Bosch J M, Sánchez Guilarte J, Rodríguez Centella C, Prieto Pareja E, Sánchez Martín J A

出版信息

Sangre (Barc). 1989 Feb;34(1):32-40.

PMID:2711282
Abstract

The aim of the present work was to perform a prospective analysis of the significance of macrocytic red cells through the study of all patients with MCV higher than 105 fl (those treated with cytotoxic or immunosuppressing drugs were excluded). Conventional clinical, haematologic and biochemical studies were carried out on every patient, along with B12 and folate levels, bone marrow examination and bone marrow karyotype and, whenever B12 deficiency was present, complete Schilling's test. Special attention was paid to the aetiological inquiry and post-therapeutical course. A series of 109 patients was collected. Decreased serum B12 rates with abnormal Schilling's test and response to parenteral therapy were present in 26 cases (24%). Of them, 22 fulfilled the diagnostic criteria for Biermer's anaemia, while in the remaining 4 there was impaired intestinal absorption. Serum or red-cell folate deficiency was found in 34 other cases (31%). Alcoholism was present in 20 of them, abnormal diet in 10, malabsorption syndrome in 2, and excessive demands in 2 others. Hence, vitamin deficiency underlay macrocytosis in 60/109 cases (55%). In the remaining 49 cases (45%) macrocytosis was not accompanying folate or B12 deficiency. Of these, severe liver disease was found in 16 patients (alcoholic in 15 and post-hepatitis in 1 case), with increased serum B12 in 10 cases and increased serum or erythrocytic folate in 3 others. Nineteen patients within this group had primary myelodysplastic syndromes (RA, 8; SRA, 4; RAEB, 7), and the remaining 14 cases had several haematological (AIHA, 4; CLL, 1, T-cell lymphoma 1, M-6, 1, and myelofibrosis with myeloid metaplasia, 2) or non-haematological diseases (heart insufficiency, 2; COPD,3).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是通过对所有平均红细胞体积(MCV)高于105飞升的患者进行研究,对大红细胞的意义进行前瞻性分析(排除接受细胞毒性或免疫抑制药物治疗的患者)。对每位患者进行了常规临床、血液学和生化研究,同时检测了维生素B12和叶酸水平、进行了骨髓检查及骨髓核型分析,并且只要存在维生素B12缺乏,就进行完整的希林试验。特别关注病因调查和治疗后的病程。收集了109例患者。26例(24%)患者血清维生素B12水平降低,希林试验异常且对肠外治疗有反应。其中,22例符合恶性贫血的诊断标准,其余4例存在肠道吸收障碍。另外34例(31%)患者存在血清或红细胞叶酸缺乏。其中20例有酗酒史,10例饮食异常,2例有吸收不良综合征,另外2例有需求过多情况。因此,60/109例(55%)患者的大细胞性贫血是由维生素缺乏引起的。其余49例(45%)患者的大细胞性贫血并未伴有叶酸或维生素B12缺乏。其中,16例患者有严重肝脏疾病(15例为酒精性肝病,1例为肝炎后肝病),10例患者血清维生素B12升高,3例患者血清或红细胞叶酸升高。该组中有19例患者患有原发性骨髓增生异常综合征(难治性贫血,8例;难治性贫血伴环形铁粒幼细胞增多,4例;难治性贫血伴原始细胞过多,7例),其余14例患有多种血液系统疾病(自身免疫性溶血性贫血,4例;慢性淋巴细胞白血病,1例,T细胞淋巴瘤1例,M-6型1例,骨髓纤维化伴髓外化生,2例)或非血液系统疾病(心力衰竭,2例;慢性阻塞性肺疾病,3例)。(摘要截断于250字)

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