侵袭上颌窦的局部晚期硬腭鳞状细胞癌伴同侧上颌成色菌病:仅仅是罕见的共存还是因果关系?

Shaivy Malik, Aneesa Ansari, Charanjeet Ahluwalia
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引用次数: 0

摘要

成色菌病是一种罕见的慢性真菌感染,通常影响下肢皮肤区域,主要发生在男性农业工人。然而,其皮外表现,特别是上颌窦,是非常罕见的,只有三个病例报道的文献。本病例报告一位59岁女性,有长期吸烟史,表现为硬腭溃疡增生性病变,后诊断为侵袭上颌窦的中分化鳞状细胞癌(SCC)。手术中,上颌窦坏死碎片在组织病理学检查中显示成色菌病,并伴有特征性硬化体。上颌成色菌病和鳞状细胞癌的同时发生是前所未有的,这对它们的病因相互作用提出了重要的问题。真菌感染可能是由创伤、皮质糜烂和侵袭性癌引起的免疫抑制引起的。这个病例强调了术中仔细评估的重要性,并强调了需要多学科的方法来有效地管理罕见的共同病理。术后治疗包括口服伊曲康唑(400mg /天)抗真菌治疗和辅助放疗。侵袭性恶性肿瘤与罕见真菌感染的独特组合强调了详细记录和探索这种非典型表现的重要性。需要进一步的研究来阐明潜在的病因联系,并为这种罕见和复杂的临床情况的诊断和管理制定循证指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Locally advanced squamous cell carcinoma of the hard palate invading the maxillary sinus with ipsilateral maxillary chromoblastomycosis: Simply a rare coexistence or a causal relationship?
Chromoblastomycosis is a rare chronic fungal infection typically affecting the cutaneous regions of the lower extremities, predominantly in male agricultural workers. However, its extracutaneous manifestations, particularly in the maxillary sinus, are exceedingly rare, with only three cases reported in the literature. This case report presents a 59-year-old female with a history of chronic tobacco use, who presented with an ulceroproliferative lesion of the hard palate, later diagnosed as moderately differentiated squamous cell carcinoma (SCC) invading the maxillary sinus. During surgery, necrotic debris in the maxillary sinus revealed chromoblastomycosis on histopathological examination, confirmed by the presence of characteristic sclerotic bodies.
The co-occurrence of maxillary chromoblastomycosis and SCC is unprecedented, raising important questions about their etiological interplay. The fungal infection may have been facilitated by trauma, cortical erosion, and immunosuppression induced by the invasive carcinoma. This case emphasizes the importance of careful intraoperative evaluation and highlights the need for a multidisciplinary approach to manage rare co-pathologies effectively. Postoperative treatment included antifungal therapy with oral itraconazole (400 mg/day) and adjuvant radiotherapy for SCC.
The unique combination of an aggressive malignancy with a rare fungal infection in this patient underscores the importance of detailed documentation and exploration of such atypical presentations. Further studies are required to elucidate potential causative links and to develop evidence-based guidelines for the diagnosis and management of such rare and complex clinical scenarios.
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