Entities of Chronic and Granulomatous Invasive Fungal Rhinosinusitis: Separate or Not?

Author:

Zhou Ling-Hong1,Wang Xuan1,Wang Rui-Ying1,Zhao Hua-Zhen1,Jiang Ying-Kui1,Cheng Jia-Hui1,Huang Li-Ping1,Chen Zhong-Qing2,Wang De-Hui3,Zhu Li-Ping1

Affiliation:

1. Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China

2. Pathology Department, Huashan Hospital, Fudan University, Shanghai, China

3. Department of Otolaryngology, Eye and Ear, Nose and Throat Hospital, Fudan University, Shanghai, China

Abstract

Abstract Background Chronic and granulomatous invasive fungal rhinosinusitis are important causes of blindness and craniocerebral complications. However, the classification of these 2 diseases remains controversial. Methods We retrospectively analyzed patients with chronic and granulomatous invasive fungal rhinosinusitus in a Chinese tertiary hospital from 2009 to 2017, with a focus on classification and comparisons. Results Among 55 patients enrolled in our study, 11 (11/55, 20%) had granulomatous invasive fungal rhinosinusitis (GIFRS) and 44 (44/55, 80%) had chronic invasive fungal rhinosinusitis (CIFRS). Aspergillus fumigatus and Dematiaceous hyphomycetes were identified in 2 patients with GIFRS. Compared with granulomatous type, CIFRS was more frequently encountered in immunocompromised patients (P = .022), and the time from onset to diagnosis was much shorter (P = .001). Proptosis and orbital apex syndrome showed no significant difference between granulomatous and CIFRS in our study. The treatment options and prognosis of both diseases also showed no significant difference. Conclusions Despite the consensus on histopathology, the classification of the chronic and granulomatous types may need further evaluation in clinical considerations.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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