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软斑病:继发于免疫抑制的后天性疾病的证据。

Malakoplakia: evidence for an acquired disease secondary to immunosuppression.

作者信息

Biggar W D, Keating A, Bear R A

出版信息

Transplantation. 1981 Feb;31(2):109-12.

PMID:7020170
Abstract

A 44-year-old man was maintained on prednisone and azathioprine after renal transplantation. One and a half years after transplantation, he developed multiple perianal Escherichia coli abscesses. These became chronic and resisted antibiotic therapy. Histologically, the lesions were typical of malakoplakia. Peripheral blood neutrophils and monocytes had impaired killing of Staphylococcus aureus and E. coli in vitro. No abnormality of hexose monophosphate pathway activity, tetrazolium dye reduction, lysosomal degranulation, or cyclic nucleotides could be demonstrated in either neutrophils or monocytes. Cholinergic agonists in vitro and in vivo did not improve bacterial killing by these cells. The infection resolved rapidly and bacterial killing returned to normal when the dose of azathioprine was reduced. Our findings, when considered with previous reports, suggest that there are different causes of malakoplakia and malakoplakia may be more common than previously thought. The etiology of malakoplakia should be identified for each patient if appropriate treatment is to be given.

摘要

一名44岁男性在肾移植后接受泼尼松和硫唑嘌呤治疗。移植后一年半,他出现了多个肛周大肠杆菌脓肿。这些脓肿转为慢性,对抗生素治疗有抵抗性。组织学上,病变为典型的软斑病。外周血中性粒细胞和单核细胞在体外对金黄色葡萄球菌和大肠杆菌的杀伤能力受损。在中性粒细胞或单核细胞中均未发现磷酸己糖途径活性、四氮唑染料还原、溶酶体脱颗粒或环核苷酸有异常。体外和体内的胆碱能激动剂均未改善这些细胞的细菌杀伤能力。当硫唑嘌呤剂量减少时,感染迅速消退,细菌杀伤能力恢复正常。我们的发现与先前的报告相结合,提示软斑病有不同的病因,且软斑病可能比以前认为的更常见。如果要给予适当治疗,应针对每位患者确定软斑病的病因。

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