免疫功能正常患者罕见的鼻-眶-皮肤粘液瘤病:病例报告。

IF 0.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pan African Medical Journal Pub Date : 2024-05-15 eCollection Date: 2024-01-01 DOI:10.11604/pamj.2024.48.13.43454
Ni Putu Ayu Reza Dhiyantari, Delfitri Lutfi, Dwi Hari Susilo, Irwan Kristyono, Alicia Widya
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引用次数: 0

摘要

粘孢子菌病是由粘孢子菌引起的一种罕见的机会性感染。皮肤粘孢子菌病通常表现为慢性惰性感染,而鼻眶粘孢子菌病则进展迅速,经常侵犯邻近的脑组织,死亡率很高。本病例代表了鼻眶-皮肤粘液瘤病的非典型临床病史。患者因右眼眶蜂窝织炎伴有广泛多发性化脓性深部皮肤感染和头痛加重而就诊。皮损源于入院前九个月右侧眶周的局部脓肿。经过数周的抗生素治疗无效后,医生怀疑是真菌感染。医生采取了积极的治疗措施,排除了右眼的感染,并进行了手术清创。对健康的眶周组织进行周期性酸性希夫染色,发现了带状菌丝,呈灰白色,90°分枝,确定为 Mucoraceaefamily。使用两性霉素 B 进行抗真菌治疗四周后,病症得到缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare presentation of rhino-orbital-cutaneous mucormycosis in an immunocompetent patient: a case report.

Mucormycosis is a rare opportunistic infection caused by Mucorales fungi. Cutaneous mucormycosis typically present as chronic indolent infection, whereas rhino-orbital mucormycosis is rapidly progressive disease often invade the adjacent cerebral tissue associated with high mortality. This case represents the atypical clinical history of rhino-orbital-cutaneous mucormycosis. The patient was presented with a right orbital cellulitis associated with an extensive multiple suppurative deep cutaneous infection and worsening headache. The skin lesion was initiated from a localized abscess at the right periorbital area nine months before admission. Suspicion of fungal infection was raised after weeks of non-responsive antibiotics treatment. Aggressive treatment with exoneration of the right eye and surgical debridement was undertaken. Periodic acid Schiff staining from healthy periorbital tissue revealed ribbon-like hyphae with pauciseptate and 90° branching identified as Mucoraceaefamily. The resolution was seen after four weeks of antifungal treatment with Amphotericin B.

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来源期刊
Pan African Medical Journal
Pan African Medical Journal PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
1.80
自引率
0.00%
发文量
691
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