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免疫功能正常患者由烟曲霉引起的原发性皮肤曲霉病:一例报告。

Primary cutaneous aspergillosis caused by Aspergillus.fumigatus in an immunocompetent patient: A case report.

作者信息

Liu Xiaoyan, Yang Jun, Ma Weiyuan

机构信息

Department of Pulmonary Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China Department of Pulmonary Medicine, Ankang Central Hospital, Ankang Department of Dermatology, Qilu Hospital, Shandong University, Jinan, China.

出版信息

Medicine (Baltimore). 2017 Dec;96(48):e8916. doi: 10.1097/MD.0000000000008916.

DOI:10.1097/MD.0000000000008916
PMID:29310381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5728782/
Abstract

RATIONALE

Primary cutaneous aspergillosis in immunocompromised patients has been well described in extensive investigations. However, in immunocompetent hosts, primary cutaneous infection of aspergillus occurs rarely, and remains poorly characterized.

PATIENT CONCERNS

We present a case of primary cutaneous aspergillosis manifested by erythematous plague covered with flava eschar.

DIAGNOSES

The patient was diagnosed with primary cutaneous aspergillosis.

INTERVENTIONS

Treatments with oral itraconazole at a dose of 75 mg/d and local wound care with ciclopirox olamine ointment were administered.

OUTCOMES

After half a month, a partial resolution and a decrease in tenderness indicated gradual improvement, and a complete remission was achieved 2 months later.

LESSONS

Primary cutaneous aspergillosis could occur in immunocompetent hosts. The initial lesions may appear in different forms, including macules, papules, nodules, or plaques. Repeated biopsy of a skin lesion for both culture and histopathology is needed.

摘要

理论依据

免疫功能低下患者的原发性皮肤曲霉病已在广泛研究中得到充分描述。然而,在免疫功能正常的宿主中,曲霉原发性皮肤感染很少发生,且特征仍不明确。

患者情况

我们报告一例原发性皮肤曲霉病病例,表现为覆盖有黄色焦痂的红斑性脓疱。

诊断

该患者被诊断为原发性皮肤曲霉病。

干预措施

给予口服伊曲康唑,剂量为75毫克/天,并使用环吡酮胺软膏进行局部伤口护理。

结果

半个月后,部分消退和压痛减轻表明病情逐渐改善,2个月后实现完全缓解。

经验教训

原发性皮肤曲霉病可发生在免疫功能正常的宿主中。初始病变可能以不同形式出现,包括斑疹、丘疹、结节或斑块。需要对皮肤病变进行反复活检以进行培养和组织病理学检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/a759a7cc1550/medi-96-e8916-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/8dbe32a5584e/medi-96-e8916-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/53fc249ce6d4/medi-96-e8916-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/a759a7cc1550/medi-96-e8916-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/8dbe32a5584e/medi-96-e8916-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/53fc249ce6d4/medi-96-e8916-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a2/5728782/a759a7cc1550/medi-96-e8916-g003.jpg

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Medicine (Baltimore). 2016 Jun;95(26):e3747. doi: 10.1097/MD.0000000000003747.
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