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Whipple 病中的肉芽肿性肺病和免疫重建炎症综合征。

Granulomatous lung disease and immune reconstitution inflammatory syndrome in Whipple's disease.

机构信息

Internal Medicine, Hospital Uster, Uster, Switzerland

Institute of Physiology, University of Zurich, Zurich, Switzerland.

出版信息

BMJ Case Rep. 2021 Jun 18;14(6):e243633. doi: 10.1136/bcr-2021-243633.

Abstract

We present the case of a 70-year-old woman with a history of seronegative arthritis, recurrent pleural effusion and weight loss. A prior lung biopsy had revealed non-caseating epithelioid cell granulomas without evidence for microbial organisms on special stains. Intestinal biopsy findings where suspicious for Whipple's disease, which was confirmed by PCR testing, both on the intestinal and retrospectively on the lung tissue. Treatment with ceftriaxone resulted in clinical deterioration with fever, arthritis and recurrent pleuritis consistent with immune reconstitution inflammatory syndrome. Dose increase of glucocorticoids and therapy rotation to doxycycline and hydroxychloroquine resulted in rapid clinical improvement.

摘要

我们报告一例 70 岁老年女性,病史为血清阴性关节炎、反复胸腔积液和体重减轻。既往肺活检显示无干酪样上皮样细胞肉芽肿,特殊染色未见微生物。肠活检提示疑诊为Whipple 病,PCR 检测结果在肠组织和回顾性肺组织中均得到证实。头孢曲松治疗后出现发热、关节炎和反复胸膜炎,符合免疫重建炎症综合征,病情恶化。增加糖皮质激素剂量并将治疗方案改为多西环素和羟氯喹后,临床状况迅速改善。

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