Barrak H A
Department of Surgery, Medical College of Basra, Iraq.
J Laryngol Otol. 2007 Nov;121(11):1099-102. doi: 10.1017/S0022215107006354. Epub 2007 Feb 26.
Mucormycosis is an opportunistic, fulminating fungal infection of the sino-nasal region. It tends to affect people with immune suppression. The hard palate is a rare site of the disease and few cases have been reported in the literature. This report discusses the nature of hard palate mucormycosis, with the aim of outlining possible explanations and reviewing associated characteristics.
This was a prospective analysis of four cases of hard palate mucormycosis. The patients were referred from the medical department, with uncontrolled diabetes mellitus. An aggressive treatment protocol was used, i.e. an intensive course of antifungal drugs and frequent debridement of dead tissue.
A painful, dusky red swelling was noticed at the early stages of the hemi-palate lesion. It was eventually followed by deep ulceration and even big perforation. Orbit and intracranial extension was the preceding sign in all instances. The progression of the perforation was not controlled by a full course of treatment. There were two deaths during the treatment course.
Mucormycosis of the hard palate is an ominous sign. Although rare, the lesion is progressive in nature and barely controlled by treatment. Clinicians should maintain a high degree of clinical suspicion in the management of patients with palatal ulcer and debilitating illness.
毛霉病是一种侵袭性的鼻窦区域机会性真菌感染。它易发生于免疫抑制人群。硬腭是该疾病的罕见发病部位,文献报道的病例较少。本报告探讨硬腭毛霉病的本质,旨在阐述可能的病因并回顾相关特征。
这是一项对4例硬腭毛霉病病例的前瞻性分析。患者由内科转诊而来,患有未得到控制的糖尿病。采用了积极的治疗方案,即强化抗真菌药物疗程并频繁清创坏死组织。
硬腭病变早期可见疼痛性暗红色肿胀。最终发展为深部溃疡甚至大穿孔。所有病例均有眼眶和颅内蔓延的迹象。整个疗程的治疗未能控制穿孔的进展。治疗过程中有2例死亡。
硬腭毛霉病是一种不祥之兆。尽管罕见,但该病变具有进行性,治疗难以控制。临床医生在处理腭部溃疡和体弱多病的患者时应保持高度的临床怀疑。