罕见的慢性鼻脑粘液瘤病病例

IF 1.6 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Marie Louise Aicher , Jeanne Bisch-Karatas , Alexander Maurer , Franca Wagner , Martin Wartenberg , Stefan Zimmerli
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引用次数: 0

摘要

我们描述了一例糖尿病患者的鼻-眶-脑粘液瘤病(ROCM)病例。她出现了海绵窦综合征和视神经缺血。最初鼻腔和副鼻窦的检查结果并不明显,因此延误了早期诊断。在两周内,随访的磁共振成像显示眶内炎症进展、海绵窦血栓形成、左中鼻孔侵蚀性破坏、左鼻腔坏死的黑色组织以及在连续进行的乙状窦切除术中显示的上颌窦破坏,最终为诊断提供了依据。通过组织病理学检查和培养,确定了确诊。治疗包括两性霉素 B 脂质体、部分手术切除和改善糖尿病控制。通过本病例报告,我们希望强调迅速诊断 ROCM 的困难,并提醒读者注意其慢性形式。2012 Elsevier Ltd. 保留所有权利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare case of a chronic rhinocerebral mucormycosis

We describe a case of rhino-orbital-cerebral mucormycosis (ROCM) in a diabetic patient. She presented with cavernous sinus syndrome and ischemia of the optic nerve. Initially unremarkable findings in the nasal cavity and paranasal sinus delayed early diagnosis. Within two weeks, a follow-up MRI showing progressive orbital inflammation, thrombosis of the cavernous sinus and erosive destruction of the left middle nasal concha together with necrotic black tissue in the left nasal cavity and destruction of the maxillary sinus demonstrated in a consecutively performed ethmoidectomy, finally gave way to diagnosis. Definite diagnosis was established by histopathology and culture. Treatment consisted of a combination of liposomal Amphotericin B, partial surgical resection and improved diabetes control. Despite insufficient surgical treatment, the progression of the disease was remarkably slow – a typical hallmark of chronic ROCM.

With this case report we aim to underline the difficulties in establishing a prompt diagnosis of ROCM and to remind readers of its chronic form.

2012 Elsevier Ltd. All rights reserved.

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来源期刊
Medical Mycology Case Reports
Medical Mycology Case Reports MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
4.00
自引率
0.00%
发文量
48
审稿时长
47 days
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