Cutaneous Mycobacterium szulgai infection in a patient with Cushing's syndrome: a case report and literature review

被引:1
|
作者
Ye, Haiyan [1 ]
Harris, Vanessa C. [2 ,3 ,4 ,5 ]
Chiu, Kelvin Hei-Yeung [6 ]
Chen, Shuang [7 ]
Xing, Fanfan [1 ]
Sun, Linlin [1 ]
Deng, Chaowen [1 ]
Yang, Jin [1 ]
Chan, Jasper Fuk-Woo [1 ,6 ,8 ]
Yuen, Kwok-Yung [1 ,6 ,8 ]
机构
[1] Univ Hong Kong, Shenzhen Hosp, Dept Infect Dis & Microbiol, Shenzhen, Guangdong, Peoples R China
[2] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Internal Med, Div Infect Dis, Amsterdam, Netherlands
[3] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Global Hlth, Amsterdam, Netherlands
[4] Univ Amsterdam, Amsterdam Univ Med Ctr, Amsterdam Inst Global Hlth & Dev, Dept Global Hlth, Amsterdam, Netherlands
[5] Amsterdam Inst Infect & Immun, Infect Dis, Amsterdam, Netherlands
[6] Queen Mary Hosp, Dept Microbiol, Pokfulam, Hong Kong, Peoples R China
[7] Univ Hong Kong, Shenzhen Hosp, Dept Pathol, Shenzhen, Guangdong, Peoples R China
[8] Univ Hong Kong, Fac Med, Carol Yu Ctr Infect Li Ka Shing, State Key Lab Emerging Infect Dis,Dept Microbiol,S, Hong Kong, Peoples R China
关键词
Mycobacterium szulgai; Cushing's syndrome; Hypercortisolism; Cutaneous infection; Case report; MULTIFOCAL OSTEOMYELITIS; PULMONARY INFECTION; SKIN;
D O I
10.1186/s12879-023-08253-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundOpportunistic infection is an under-recognized complication of Cushing's syndrome, with infection due to atypical mycobacterium rarely reported. Mycobacterium szulgai commonly presents as pulmonary infection, with cutaneous infection seldom reported in the literature.Case Presentation48-year-old man with a newly-diagnosed Cushing's syndrome secondary to adrenal adenoma presented with a subcutaneous mass on the dorsum of his right hand, was diagnosed with cutaneous Mycobacterium szulgai infection. The most likely source of the infection was through minor unnoticed trauma and inoculation from a foreign body. The patient's Cushing's syndrome, high serum cortisol levels and secondary immune suppression facilitated mycobacterial replication and infection. The patient was successfully treated with adrenalectomy, surgical debridement of cutaneous lesion, and a combination of rifampicin, levofloxacin, clarithromycin, and ethambutol for 6 months. There were no signs of relapse one year after cessation of anti-mycobacterial treatment. A literature review on cutaneous M. szulgai infection to further characterize the clinical characteristics of this condition, identified 17 cases of cutaneous M. szulgai infection in the English literature. Cutaneous M. szulgai infections with subsequent disease dissemination are commonly reported in immunocompromised hosts (10/17, 58.8%), as well as in immunocompetent patients with a history of breached skin integrity, such as invasive medical procedures or trauma. The right upper extremity is the most commonly involved site. Cutaneous M. szulgai infection is well controlled with a combination of anti-mycobacterial therapy and surgical debridement. Disseminated infections required a longer duration of therapy than localized cutaneous infections. Surgical debridement may shorten the duration of antibiotics.ConclusionsCutaneous M. szulgai infection is a rare complication of adrenal Cushing's syndrome. Further studies are needed to provide evidence-based guidelines on the best combination of anti-mycobacterial and surgical therapy for managing this rare infective complication.
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