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髓过氧化物酶缺乏症合并播散性副球孢子菌病和腹膜结核的病例报告

Case report of myeloperoxidase deficiency associated with disseminated paracoccidioidomycosis and peritoneal tuberculosis.

作者信息

Domingues-Ferreira Maurício, Levy Ariel, Barros Noac Chuffi, Bertolini Dalton Luis, Vasconcelos Dewton de Moraes

机构信息

Ambulatório das Manifestações Cutâneas das Imunodeficiência Primárias, Departamento de Dermatologia, Hospital das Clinicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.

出版信息

Rev Soc Bras Med Trop. 2017 Jul-Aug;50(4):568-570. doi: 10.1590/0037-8682-0462-2016.

Abstract

Myeloperoxidase (MOP) is present in monocyte and neutrophil lysosomes, catalyzing hydrogen peroxide and chloride ion conversion to hypochlorous acid. MOP seems to destroy pathogens during phagocytosis by neutrophils and is considered an important defense against innumerous bacteria. We present a patient who had MOP deficiency, who presented with a subacute form of paracoccidioidomycosis and later with peritoneal tuberculosis. MOP deficiency leads to the diminished destruction of phagocytized pathogens. This case gives important evidence of an association between MOP deficiency and increased susceptibility to infection by Paracoccidioides brasiliensis and Mycobacterium tuberculosis.

摘要

髓过氧化物酶(MOP)存在于单核细胞和中性粒细胞的溶酶体中,催化过氧化氢和氯离子转化为次氯酸。MOP似乎在中性粒细胞吞噬作用期间破坏病原体,被认为是抵御众多细菌的重要防御机制。我们报告了一名患有MOP缺乏症的患者,该患者最初表现为亚急性副球孢子菌病,后来又出现了结核性腹膜炎。MOP缺乏导致吞噬的病原体破坏减少。该病例为MOP缺乏与巴西副球孢子菌和结核分枝杆菌感染易感性增加之间的关联提供了重要证据。

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