您的位置: 百康网 > 期刊 > 皮肤病学与性病学 > 《传染病的形成》 > 2005年 > 2005年2月第2期 > 正文
Imported Cutaneous Diphtheria, Germany, 1997–2003
 本页关键词:Diphtheria
2007-6-14 16:48:37

    Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, Munich, Germany

    To the Editor: The March 2004 report by de Benoist et al. on the incidence of imported cutaneous diphtheria in the United Kingdom (1) prompted us to describe the situation of cutaneous diphtheria in Germany and to analyze the cases reported to the German Consiliary Laboratory on Diphtheria since its establishment at our institute in 1997. The laboratory provides advisory and diagnostic services mainly to microbiologic laboratories throughout Germany.

    From 1997 to 2003, 6 cases of cutaneous infections caused by toxigenic Corynebacterium diphtheriae were documented (Table). None of these was accompanied by secondary diphtheria infection. Toxigenicity was determined by both dtx polymerase chain reaction and Elek test (2). As in the United Kingdom, all cases for which clinical information was available (N = 5) were imported. Three were found in tourists who had traveled to tropical countries: a 20-year-old diver had injured her heel after stepping on coral in Thailand; a 60-year-old tourist had a chronic ulcer in the thigh after a trip to Indonesia (no history of an insect bite); and a 39-year-old traveler to Kenya returned with a purulent ear infection with no memory of trauma or insect bite. The remaining imported C. diphtheriae skin infections were reported in 2 Angolan children, 5 and 10 years of age, who were brought to Germany by a humanitarian organization for surgery on severe gun wounds to their lower extremities (foot and thigh with chronic osteomyelitis, respectively). To our knowledge, these reports are the first of cutaneous diphtheria in gunshot wounds in recent years. Moreover, in the patient with the thigh wound, C. diphtheriae was also isolated from a deep fistula, which suggests involvement of C. diphtheriae in the chronic osteomyelitis.

    As in the United Kingdom, all cases of diphtheria reported since 1997 were caused by C. diphtheriae mitis. In 4 of 5 cutaneous diphtheria patients who had an available medical history, mixed infections with Staphylococcus aureus and Streptococcus pyogenes were found; 3 of 5 patients were not sufficiently vaccinated against diphtheria as recommended. Systemic symptoms, such as malaise and general weakness, developed in the 20-year-old Thailand tourist, although she had received a booster dose just before her travel. Cutaneous diphtheria must be expected even in vaccinated patients; for instance, among serum samples of 287 healthy German adults with a complete record of basic immunization against diphtheria, only 42.2% showed full serologic protection as indicated by antitoxin levels >0.1 IU/mL (3).

    As de Benoist et al. outline, cutaneous diphtheria might be difficult to diagnose because of its unspecific clinical appearance and the presence of mixed infections in chronic nonhealing skin lesions. Because of the nearly complete disappearance of cutaneous diphtheria in many parts of the western world, microbiologists lack experience in identifying C. diphtheriae grown from specimens. From 1997 to 2003, approximately one fifth of the strains sent to our Consiliary Laboratory on Diphtheria for species identification and toxin testing were either nondiphtheria Corynebacterium spp. or noncoryneform bacteria of different genera (including lactobacilli, Dermabacter hominis, and Propionibacterium acnes).

    Clinicians (4) and microbiologists (5) should be aware of the possibility of cutaneous diphtheria in chronically infected skin lesions in patients returning from disease-endemic regions. Medical personnel should include this in civilian as well as military health services, since our cases indicate that toxigenic C. diphtheriae might affect not only travel-related skin injuries caused by leisure or tourist activities but also wounds in patients from war regions in diphtheria-endemic areas.

    References

    De Benoist AC, White JM, Efstratiou A, Kelly C, Mann G, Nazareth B, et al. Imported cutaneous diphtheria, United Kingdom. Emerg Infect Dis. 2004;10:511–3.

    Sing A, Hogardt M, Bierschenk S, Heesemann J. Detection of differences in the nucleotide and amino acid sequences of diphtheria toxin from Corynebacterium diphtheriae and Corynebacterium ulcerans causing extrapharyngeal infections. J Clin Microbiol. 2003;41:4848–51.

    Hasselhorn HM, Nubling M, Tiller FW, Hofmann F. Factors influencing immunity against diphtheria in adults. Vaccine. 1998;16:70–5.

    Bonnet JM, Begg NT. Control of diphtheria: guidance for consultants in communicable disease control. Commun Dis Public Health. 1999;2:242–9.

    Efstratiou A, George RC. Laboratory guidelines for the diagnosis of infections caused by Corynebacterium diphtheriae and C. ulcerans. Commun Dis Public Health. 1999;2:250–7.



查询更多Diphtheria相关信息在本站>>

  

《传染病的形成》2005年2月第11卷第2期 

评论】【打印】【 】【关闭
相关文章
Eagle Effect in Corynebacterium diphtheriae
The Protein Content of Diphtheria-Tetanus ToxoidsAcellular Pertussis Vaccines and an Emerging Clinical Problem
Suppression and Modulation of Cellular and Humoral Immune Responses to Haemophilus influenzae Type B (Hib) Conjugate Vaccine in HibDiphtheria-Tetanus ToxoidsAcellular Pertussis Combination Vaccines: A
The Diphtheria and Pertussis Components of Diphtheria-Tetanus ToxoidsPertussis Vaccine Should Be Genetically Inactivated Mutant Toxins
Managing Febrile Respiratory Illnesses during a Hypothetical SARS Outbreak
Carbapenemase-producing Enterobacteriaceae, U.S. Rivers
Rickettsial Infection in Animals and Brazilian Spotted Fever Endemicity
Isolation of Waddlia malaysiensis, A Novel Intracellular Bacterium, from Fruit Bat (Eonycteris spelaea)
Wild Animal Mortality Monitoring and Human Ebola Outbreaks, Gabon and Republic of Congo, 2001–2003
Quarantine for SARS, Taiwan