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[大剂量皮质激素治疗伴有粒细胞缺乏症的费尔蒂综合征。3例报告]

[Treatment of Felty's syndrome accompanied by agranulocytosis using high-dose corticoids. 3 cases].

作者信息

Job-Deslandre C, Menkes C J

出版信息

Presse Med. 1987 Apr 4;16(12):569-70.

PMID:2952952
Abstract

Three cases of severe Felty's syndrome (neutrophils 80/mm3 in 2 cases and 800/mm3 in one) with enlarged spleen (1 case) and leg ulcer (2 cases) were treated with high doses of corticosteroids (methylprednisolone 1 g by intravenous infusion over 3 hours, on 3 consecutive days). In all 3 patients a dramatic result was obtained, the granulocytes returning to normal values in 24 to 48 hours. In 2 cases, an early relapse (1 month) required a second course in high dosage; after a follow-up of 36 and 8 months respectively, the number of granulocytes remains stable under prednisone 5 to 10 mg/day. The third patient was improved by one single course of infusions and remains stable after 18 months. It must be noted that one patient had previously been treated with plasma exchange and another with corticosteroids without any significant result.

摘要

3例重症费尔蒂综合征(2例中性粒细胞计数为80/mm³,1例为800/mm³)患者,其中1例有脾肿大,2例有腿部溃疡,接受了大剂量皮质类固醇治疗(甲基泼尼松龙1g,静脉输注3小时,连续3天)。所有3例患者均取得显著疗效,粒细胞在24至48小时内恢复至正常水平。2例患者在1个月时出现早期复发,需要再次进行高剂量治疗;分别随访36个月和8个月后,粒细胞数量在泼尼松5至10mg/天的剂量下保持稳定。第3例患者仅通过一个疗程的输注治疗后病情改善,18个月后保持稳定。必须指出的是,1例患者此前接受过血浆置换治疗,另1例接受过皮质类固醇治疗,但均未取得显著效果。

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