Celis-Aguilar Erika, Burgos-Páez Alan, Villanueva-Ramos Nadia, Solórzano-Barrón José, De La Mora-Fernández Alma, Manjarrez-Velázquez Juan, Verdiales-Lugo Sergio, Escobar-Aispuro Lucero, Becerril Perla, Valdez-Flores Ana, Merino-Ramírez Francisco Javier, Caballero-Rodríguez Carmen Beatriz
Department of Otolaryngology, Centro de Investigación y Docencia en Ciencias de la Salud (CIDOCS) de la Universidad Autónoma de Sinaloa, Culiacán, Sinaloa, México.
Department of Otolaryngology, Culiacan General Hospital, Culiacán, Sinaloa, México.
Int Arch Otorhinolaryngol. 2019 Jan;23(1):92-100. doi: 10.1055/s-0038-1667005. Epub 2018 Oct 24.
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. To describe the clinical characteristics and management of patients with indolent mucormycosis. In the project of study with chart review in the Interinstitutional secondary care centers, patients with evidence of indolent mucormycosis, 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. 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 symptoms were nonspecific: facial pain/headache, mucoid discharge and cacosmia were the ones most frequently reported. Maxillary sinus involvement was present in all patients. Two immunosuppressed subjects received amphotericin. Posaconazole was the only treatment in one immunosuppressed patient. All immunocompetent patients had single paranasal sinus disease and received only surgical treatment. All patients are alive and free of disease. 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.
惰性或慢性毛霉菌病是一种罕见的疾病,可影响免疫功能低下和免疫功能正常的个体。此外,其临床进展不具有特异性,且针对这种疾病尚无标准化的治疗方法。
描述惰性毛霉菌病患者的临床特征及治疗方法。
在一项对机构间二级医疗中心病历进行回顾的研究项目中,纳入了有惰性毛霉菌病证据的患者,惰性毛霉菌病定义为鼻/鼻窦毛霉菌病经病理确诊超过1个月。所有患者均接受了全面的实验室检查、影像学检查、手术治疗及充分的随访。当患者后续活检未发现毛霉菌病证据时,则定义为无疾病状态。
我们纳入了7例患者,其中3例女性,4例男性。平均年龄为53.14岁。4例免疫功能低下,3例免疫功能正常。在免疫功能低下的患者中,3例患有糖尿病,1例患有皮肌炎。症状不具有特异性:面部疼痛/头痛、黏液样分泌物及嗅觉障碍是最常报告的症状。所有患者均有上颌窦受累。2例免疫功能低下的患者接受了两性霉素治疗。1例免疫功能低下的患者仅接受了泊沙康唑治疗。所有免疫功能正常的患者均为单鼻窦疾病,仅接受了手术治疗。所有患者均存活且无疾病。
惰性毛霉菌病是免疫功能低下和免疫功能正常患者中一种新出现的临床疾病。单鼻窦疾病是常见表现,在这些患者的鉴别诊断中不应被忽视。免疫功能正常的患者仅应接受手术治疗。