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白塞病合并侵袭性肺曲霉病及耳曲霉感染:一例报告

Behçet's disease with invasive pulmonary aspergillosis and Aspergillus auriculatus infection: A case report.

作者信息

Sun Fenfen, Cao Hui, Wang Fan, Cao Guoqiang

机构信息

Department of Respiratory Disease.

Department of Radiology, Daping Hospital, Army Medical University, Chongqing, China.

出版信息

Medicine (Baltimore). 2020 Feb;99(6):e18938. doi: 10.1097/MD.0000000000018938.

DOI:10.1097/MD.0000000000018938
PMID:32028403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7015660/
Abstract

RATIONALE

Behçet's disease (BD) is an inflammatory disease that leads to multisystemic immune dysfunction and that involves pulmonary system alterations.

PATIENT CONCERNS

A 26-year-old woman presented with dull right chest pain for 30 days and intermittent cough with expectoration for 5 days. She had a history of recurrent oral ulcer and constitutional rash 2 months prior.

DIAGNOSES

The patient was diagnosed with BD complicated by IPA and Aspergillus auriculatus infection.

INTERVENTIONS

The patient was administered itraconazole oral solution (200 mg b.i.d) to treat the fungal infection. After a diagnosis of BD was made, she received 40 mg of methylprednisolone sodium succinate daily for 1 week.Then, she also received 24 mg of methylprednisolone sodium succinate daily, which was decreased by 2 mg per half month, until the rash had resolved. The patient continued to receive 200 mg Q. D itraconazole orally for 3 months. Thereafter, itraconazole was stopped, while daily oral administration of 10 mg of methylprednisolone sodium succinate was continued.

OUTCOMES

The rash was observed to resolve, and CT revealed that the lesions in both the right and left lung were reduced. During a telephone follow-up performed after 6 months, the patient stated that no symptoms had recurred during the follow-up period.

LESSONS

This case illustrates that for patients with BD, ignoring extrapulmonary symptoms often leads to a delayed diagnosis. Physicians should perform a thorough medical history and physical examination of these patients, as the information obtained in this manner may provide important clues for disease diagnosis and treatment.

摘要

理论依据

白塞病(BD)是一种导致多系统免疫功能障碍并累及肺部系统改变的炎症性疾病。

患者情况

一名26岁女性,右胸钝痛30天,伴有间断咳嗽咳痰5天。她在2个月前有复发性口腔溃疡和全身性皮疹病史。

诊断

该患者被诊断为白塞病合并侵袭性肺曲霉病(IPA)及耳曲霉菌感染。

干预措施

给予患者口服伊曲康唑溶液(200mg,每日2次)治疗真菌感染。确诊白塞病后,给予患者每日40mg甲泼尼龙琥珀酸钠,共1周。之后,给予患者每日24mg甲泼尼龙琥珀酸钠,每半月减量2mg,直至皮疹消退。患者继续口服伊曲康唑200mg,每日1次,共3个月。此后,停用伊曲康唑,继续每日口服10mg甲泼尼龙琥珀酸钠。

结果

观察到皮疹消退,CT显示左右肺病灶均缩小。6个月后电话随访,患者表示随访期间无复发症状。

经验教训

该病例表明,对于白塞病患者,忽视肺外症状常导致诊断延迟。医生应对这些患者进行全面的病史询问和体格检查,因为以此方式获得的信息可能为疾病的诊断和治疗提供重要线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f4/7015660/28af12f492cb/medi-99-e18938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f4/7015660/28af12f492cb/medi-99-e18938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f4/7015660/28af12f492cb/medi-99-e18938-g001.jpg

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A 27-Year-Old Man With Multiple Cavitary Lung Lesions.一名 27 岁男性,多发空洞性肺部病变。
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