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抗干扰素-γ自身抗体相关的播散性脓肿分枝杆菌感染酷似伴多发转移的腮腺癌:一例报告

Anti-interferon-γ autoantibody-associated disseminated Mycobacterium abscessus infection mimicking parotid cancer with multiple metastases: A case report.

作者信息

Chang Po-Hsiung, Chuang Yu-Chung

机构信息

School of Medicine, Taipei Medical University Department of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.

出版信息

Medicine (Baltimore). 2017 Sep;96(39):e8118. doi: 10.1097/MD.0000000000008118.

DOI:10.1097/MD.0000000000008118
PMID:28953638
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5626281/
Abstract

RATIONALE

Among the nontuberculous mycobacteria, Mycobacterium abscessus is a common cause of skin, soft tissue, and bone infections. However, disseminated M. abscessus infection that mimics cancer metastasis with an underlying relatively immunocompetent condition has rarely been reported.

PATIENT CONCERNS

A nonsmoking 73-year-old man with an underlying relatively immunocompetent condition reported a 2-month history of a mass in the region of his right parotid gland that had been steadily increasing in size.

DIAGNOSES

The head and neck computed tomography showed an avidly enhancing tumor with central necrosis in the right parotid region and lymphadenopathy bilaterally at neck levels II-V (<6 cm) with a necrotic core. The radiologist and otolaryngologist both suspected a diagnosis of right parotid gland cancer with metastasis.

INTERVENTIONS

The necrotic tissue was removed surgically, and Mycobacterium culture showed M. abscessus. We collected a blood sample and detected anti-interferon-γ autoantibody.

OUTCOMES

After 6 months of anti-M. abscessus treatment, physical examination showed remission of the parotid tumor, and axillary and supraclavicular lymphadenopathy.

LESSONS

We report a case of disseminated M. abscessus infection, which involved parotid glands with multiple lymphadenopathies in a person with an underlying relatively immunocompetent condition. Possible underlying mechanisms such as anti-interferon-γ autoantibody-associated immunodeficiency should be considered in a patient with disseminated M. abscessus infection without a known immunocompromised condition.

摘要

理论依据

在非结核分枝杆菌中,脓肿分枝杆菌是皮肤、软组织和骨感染的常见病因。然而,在基础免疫功能相对正常的情况下,模仿癌症转移的播散性脓肿分枝杆菌感染鲜有报道。

患者情况

一名73岁不吸烟男性,基础免疫功能相对正常,报告右侧腮腺区域有一肿物,大小持续增大2个月。

诊断

头颈部计算机断层扫描显示右侧腮腺区域有一强化明显的肿瘤,中央坏死,双侧颈部II - V级淋巴结肿大(<6厘米),有坏死核心。放射科医生和耳鼻喉科医生均怀疑为右侧腮腺癌伴转移。

干预措施

手术切除坏死组织,脓肿分枝杆菌培养显示为脓肿分枝杆菌。采集血样检测到抗干扰素-γ自身抗体。

结果

经过6个月的抗脓肿分枝杆菌治疗,体格检查显示腮腺肿瘤及腋窝和锁骨上淋巴结肿大消退。

经验教训

我们报告了一例播散性脓肿分枝杆菌感染病例,该病例发生在一名基础免疫功能相对正常的患者身上,累及腮腺并伴有多处淋巴结肿大。对于无已知免疫功能低下情况的播散性脓肿分枝杆菌感染患者,应考虑抗干扰素-γ自身抗体相关免疫缺陷等潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b249/5626281/7094dbe23ac1/medi-96-e8118-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b249/5626281/ba65c6e89503/medi-96-e8118-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b249/5626281/7094dbe23ac1/medi-96-e8118-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b249/5626281/ba65c6e89503/medi-96-e8118-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b249/5626281/7094dbe23ac1/medi-96-e8118-g002.jpg

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