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首页> 外文期刊>International Archives of Otorhinolaryngology >An Emergent Entity: Indolent Mucormycosis of the Paranasal Sinuses. A Multicenter Study
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An Emergent Entity: Indolent Mucormycosis of the Paranasal Sinuses. A Multicenter Study

机译:紧急实体:鼻窦的惰性毛霉菌病。多中心研究

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Introduction Indolent or chronic mucormycosis is a rare entity that affects both immunosuppressed and immunocompetent individuals. Additionally, its clinical evolution is nonspecific and there is no standardized treatment for this condition. Objective To describe the clinical characteristics and management of patients with indolent mucormycosis. Methods In the project of study with chart review in the Interinstitutional secondary care centers, patients with evidence of indolentmucormycosis, defined as pathological confirmation of nasal/paranasal sinus mucormycosis for more than 1 month, were included. All patients underwent complete laboratory workup, imaging studies, surgical treatment and adequate follow-up. No evidence of disease status was defined when patient had subsequent biopsies with no evidence of mucormycosis. Results We included seven patients, three female and four male subjects. The mean age was 53.14 years. Four patients were immunosuppressed and three immunocompetent. Among the immunosuppressed patients three had diabetes and one had dermatomyositis. The symptomswere nonspecific: facial pain/headache, mucoid discharge and cacosmiawere the ones most frequently reported. Maxillary sinus involvement was present in all patients. Two immunosuppressed subjects received amphotericin. Posaconazole was the only treatmentinoneimmunosuppressedpatient. Allimmunocompetent patientshadsingleparanasal sinus disease and received only surgical treatment. All patients are alive and free of disease. Conclusion Indolent mucormycosis is a new and emerging clinical entity in immunosuppressed and immunocompetent patients. Single paranasal sinus disease is a frequent presentation and should not be overlooked as a differential diagnosis in these patients. Immunocompetent patients should only be treated surgically.
机译:简介惰性或慢性毛霉菌病是一种罕见的实体,会同时影响免疫抑制和免疫能力强的个体。另外,它的临床发展是非特异性的,并且没有针对这种情况的标准化治疗。目的描述惰性黏液霉菌病的临床特点和治疗方法。方法在机构间二级护理中心进行图表审查的研究项目中,纳入具有吲哚齿状霉菌病证据的患者,这些证据被定义为经鼻/副鼻窦窦性霉菌病的病理证实超过1个月。所有患者均接受了完整的实验室检查,影像学检查,手术治疗和足够的随访。当患者随后进行活检而没有毛霉菌病的证据时,则没有疾病状态的证据。结果我们纳入了7名患者,其中3名是女性,4名是男性。平均年龄为53.14岁。免疫抑制4例,免疫抑制3例。在免疫抑制的患者中,三人患有糖尿病,一人患有皮肌炎。症状是非特异性的:面部疼痛/头痛,粘液样分泌物和粘膜炎是最常报告的症状。所有患者均出现上颌窦受累。两名免疫抑制的受试者接受了两性霉素。泊沙康唑是唯一被免疫抑制的患者。所有具有免疫功能的患者患有鼻旁窦疾病,仅接受手术治疗。所有患者都活着并且没有疾病。结论顽固性毛霉菌病是免疫抑制和免疫能力强的患者的新兴临床实体。单鼻旁窦疾病是一种常见症状,在这些患者中作为鉴别诊断不容忽视。具有免疫功能的患者应仅接受手术治疗。

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