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播散性骨骼隐球菌病:一例报告

Disseminated Skeletal Cryptococcosis: A Case Report.

作者信息

Joseph David, Paul Prannoy, Padmanabhan Vishnu, Rajesh Athul, Vignesh Raj, Baby Raphael

机构信息

Department of Orthopaedics, Government Medical College, Kozhikode, Kerala, India.

Department of Orthopaedics, M.O.S.C Medical College Hospital, Ernakulam, Kerala, India.

出版信息

J Orthop Case Rep. 2025 Aug;15(8):130-134. doi: 10.13107/jocr.2025.v15.i08.5912.

DOI:10.13107/jocr.2025.v15.i08.5912
PMID:40786765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12328977/
Abstract

INTRODUCTION

Cryptococcus is a rare cause of osteomyelitis, especially in immunocompromised individuals. This case report discusses a rare case of disseminated cryptococcosis with multiple bone lesions in a patient with isolated CD4 lymphocytopenia.

CASE REPORT

A 31-year-old apparently normal Indian male presented with pain and swelling of his right proximal femur for 8 months without any history of trauma. He also reported a similar swelling in his chest wall with allergic respiratory symptoms for 8 years. Laboratory analysis revealed mild elevation in inflammatory markers. Magnetic resonance imaging of the pelvis revealed osteolytic lesions in the right proximal femur and pubic bone with soft tissue collections, and computed tomography scan of the chest showed an osteolytic lesion in the right 9th rib with an overlying soft tissue collection and a subpleural cavitary nodule in the left lower lobe posterior basal segment. Although initially treated as a case of clinically diagnosed tuberculosis, the patient did not get any relief with antitubercular therapy. Fine needle aspiration cytology and fungal culture identified Cryptococcus neoformans from both lesions and from the blood culture. The patient responded well to antifungal treatment and is currently symptom free.

CONCLUSION

Cryptococcosis should be considered as a rare differential diagnosis in patients presenting with bone pain and multiple lytic lesions. Definitive diagnosis requires a fungal culture from the affected areas. Early treatment with antifungals is important in preventing complications and death.

摘要

引言

隐球菌是骨髓炎的罕见病因,尤其在免疫功能低下的个体中。本病例报告讨论了一例罕见的播散性隐球菌病,该患者为孤立性CD4淋巴细胞减少症,伴有多处骨病变。

病例报告

一名31岁表面上健康的印度男性,右股骨近端疼痛和肿胀8个月,无任何外伤史。他还报告胸壁有类似肿胀并伴有过敏性呼吸道症状8年。实验室分析显示炎症标志物轻度升高。骨盆磁共振成像显示右股骨近端和耻骨有溶骨性病变并伴有软组织肿物,胸部计算机断层扫描显示右第9肋骨有溶骨性病变,上方有软组织肿物,左肺下叶后基底段有一个胸膜下空洞结节。尽管最初被诊断为临床诊断的结核病,但患者接受抗结核治疗后并无缓解。细针穿刺细胞学检查和真菌培养从两个病变部位及血培养中均鉴定出新型隐球菌。患者对抗真菌治疗反应良好,目前无症状。

结论

对于出现骨痛和多处溶骨性病变的患者,应将隐球菌病视为一种罕见的鉴别诊断。明确诊断需要从受影响区域进行真菌培养。早期使用抗真菌药物治疗对于预防并发症和死亡很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/bba1d4505f16/JOCR-15-130-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/40c07abbfa92/JOCR-15-130-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/40432bc58473/JOCR-15-130-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/b06e6df7b37a/JOCR-15-130-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/082aa7369219/JOCR-15-130-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/bba1d4505f16/JOCR-15-130-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/40c07abbfa92/JOCR-15-130-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/40432bc58473/JOCR-15-130-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/b06e6df7b37a/JOCR-15-130-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/082aa7369219/JOCR-15-130-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a364/12328977/bba1d4505f16/JOCR-15-130-g006.jpg

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