Jung Sang-Hee, Kim Sung Won, Park Chan Soon, Song Chang Eun, Cho Jin Hee, Lee Joo Hyung, Kim Nam Sik, Kang Jun Myung
Department of Otolaryngology-Head and Neck Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Auris Nasus Larynx. 2009 Jun;36(3):274-9. doi: 10.1016/j.anl.2008.07.003. Epub 2008 Sep 10.
Rhinocerebral mucormycosis is rare, rapidly progressive, potentially life-threatening disease, and it usually occurs in immunocompromised patients. We present our clinical experience with 12 cases and we attempt to identify the prognostic features and proper treatment protocols.
All the cases of mucormycosis were proven by histology or culture. The prognosis was analyzed according to the predisposing factors, including underlying disease, extent of disease and surgical intervention.
The overall mortality rate in our series was 33.3%. 7 of the 10 operated patients recovered, while 1 of the 2 non-operated patients expired. The associated conditions included diabetes mellitus (n=9) and hematological disease (n=3). A poor prognosis was primarily related with uncontrolled underlying disease. Other associated prognostic factors were the extent of disease including orbital or intracranial extension. Surgical debridement is essential for a good prognosis, but timely intervention and complete aggressive debridement are not always needed in all patients. The patient who had slowly progressive disease also survived after conventional medical management and limited surgical debridement, including orbital preservation.
Control of the underlying predisposing illness along with prompt parenteral administration of amphotericin B and aggressive surgical debridement remain the essential treatments even today. Contrary to this, as described in this study, for the patients with slowly progressive disease, the aggressive surgical debridement is spared, and a successful result may be obtained with the conventional management, including medical treatment and timely limited surgical intervention.
鼻脑型毛霉菌病是一种罕见的、进展迅速、可能危及生命的疾病,通常发生在免疫功能低下的患者中。我们介绍了12例患者的临床经验,并试图确定预后特征和合适的治疗方案。
所有毛霉菌病病例均经组织学或培养证实。根据诱发因素分析预后,包括基础疾病、疾病范围和手术干预。
我们系列病例的总死亡率为33.3%。10例接受手术的患者中有7例康复,而2例未接受手术的患者中有1例死亡。相关疾病包括糖尿病(n = 9)和血液系统疾病(n = 3)。预后不良主要与基础疾病控制不佳有关。其他相关的预后因素是疾病范围,包括眼眶或颅内扩展。手术清创对于良好的预后至关重要,但并非所有患者都始终需要及时干预和彻底积极的清创。病情进展缓慢的患者在接受传统药物治疗和有限的手术清创(包括保留眼眶)后也存活下来。
即使在今天,控制基础诱发疾病、及时胃肠外给予两性霉素B和积极的手术清创仍然是基本的治疗方法。与此相反,如本研究所述,对于病情进展缓慢的患者,可以避免积极的手术清创,通过包括药物治疗和及时有限的手术干预在内的传统治疗方法可能会取得成功的结果。