Case Report: Clinical and Pathological Findings of Tuberculous Gumma: A Case Report and Literature Review

Li-Jia Deng Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China;

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Qian Ye Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China;
Department of Dermatology, Plastic Surgery Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China

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Si-Yu Luo
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Qin-Xiao Wang Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China;

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Sheng Fang Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China;

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ABSTRACT.

Tuberculous gumma (TG) is a rare type of cutaneous tuberculosis thought to occur as a result of the hematogenous spread of Mycobacterium tuberculosis, which is more common in immunosuppressed individuals. An 8-year-old boy presented with a 2-month history of multiple indolent enlarging ulcerated nodules on his left upper extremity. He had a past medical history of bacille Calmette–Guerin vaccine induced lupus vulgaris. Skin biopsy of the nodules showed granulomas and neutrophil-dominated purulent inflammation. Ziehl–Neelsen staining was negative, and the cultures were positive for M. tuberculosis. Furthermore, the M. tuberculosis complex was identified using metagenomic next-generation sequencing. Standard antitubercular therapy was started at full doses, and the skin lesions had significantly improved 3 months later. Here we review the literature since 2000 and describe the clinical and pathological features of TG.

Author Notes

Disclosure: Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article. This is a retrospective case study. The First Affiliated Hospital Ethics Committee has confirmed that no ethical approval is required. The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding authors.

Authors’ addresses: Li-Jia Deng, Si-Yu Luo, Qin-Xiao Wang, and Sheng Fang, Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China, E-mails: denglijiaderm@yeah.net; siyuluoderm@yeah.net; qinxiaowangderm@yeah.net; fangshengderm@163.com. Qian Ye, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China and Department of Dermatology, Plastic Surgery Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China, E-mail: yeqian0330@163.com.

Address correspondence to Sheng Fang, Department of Dermatology, The First Affiliated Hospital of Chongqing Medical University, No. 1 Youyi Road, Yuzhong District, Chongqing 400016, China. E-mail: fangshengderm@163.com
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