具有分支体的播散性黄球霉菌性淋巴结炎

Safia Moin, F. Mahmood, J. Farooqi, Faheem Naqvi, Romana Idress, K. Jabeen, A. Zafar
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摘要

目的:本研究描述一例年轻女性播散性黄细胞性淋巴结炎,诊断延迟,经适当治疗后临床反应良好。方法:一位32岁的女性,其腹股沟区出现红斑至紫罗兰色丘疹,并伴有双侧渗出物,持续数月。病史显示,结核性脑膜炎4年前接受了18个月的一线抗结核治疗,2年前她腋窝两侧出现色素性淋巴结排出。腋窝淋巴结活检的组织病理学表现为慢性肉芽肿性炎症,伴有多分支分隔真菌菌丝。她接受两性霉素B治疗21天,但没有好转。腹股沟病变的活检被送去进行组织病理学和培养。结果:活检材料的组织病理学显示慢性肉芽肿性炎症过程,有多核巨细胞、上皮样细胞、组织细胞和淋巴细胞,并有多分支分隔真菌菌丝。革兰氏染色显示中等间隔的菌丝和大量的脓细胞。在沙氏葡萄糖琼脂上培养第四周产生天鹅绒般的橄榄黑色菌落。培养材料的显微镜载玻片检查提示了枝藻属物种。患者开始服用伏立康唑,持续服用6个月,临床症状有所改善。结论:对感染性病变的调查不全面可能延误诊断。此外,临床表现在很大程度上受宿主免疫状态的影响。组织病理学和微生物学评估对于做出结论性诊断同样重要。抗真菌治疗可能会延迟正常生长的真菌在一周内的生长;因此,真菌涂片阳性样本可能需要更长的培养时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disseminated Phaeohyphomycotic Lymphadenitis with Cladophialophora Species
Objective: This study describes a case of disseminated phaeohyphomycotic lymphadenitis in a young female with delayed diagnosis and good clinical response after appropriate treatment. Methods: A 32-year-old female presented with erythematous to violaceous papules with oozing discharge bilaterally in her inguinal region for a few months. History revealed tuberculous meningitis 4 years earlier treated with first line anti-tuberculous therapy for 18 months, and 2 years previously she developed pigmented discharging lymph nodes bilaterally in her axillae. The histopathology of the biopsy of the axillary nodes showed chronic granulomatous inflammation with multiple branching septate fungal hyphae. She received amphotericin B for 21 days but without improvement. Biopsy from the inguinal lesions was sent for histopathology and culture. Results: Histopathology of the biopsy material showed chronic granulomatous inflammatory process with multinucleate giant cells, epithelioid cells, histiocytes, and lymphocytes with multiple branching septate fungal hyphae. Gram stain revealed moderate septate hyphae with numerous pus cells. Culture on Sabouraud dextrose agar yielded velvety olive–black colonies in the fourth week. Microscopic slide examination of culture material was suggestive of Cladophialophora species. The patient was started on voriconazole, which was continued for 6 months, and showed clinical improvement. Conclusion: Incomplete investigation of infectious lesions may delay diagnosis. Furthermore, clinical presentations are greatly influenced by the immune status of the host. Both histopathological and microbiological assessments are equally important for making a conclusive diagnosis. Anti-fungal therapy may delay the growth of fungi that normally grow within a week; thus, a longer incubation time may be warranted for fungal smear-positive samples.
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