ActinomycosisA42.9

Author:Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 15.06.2022

Dieser Artikel auf Deutsch

Synonym(s)

Actinomycosis; Cervicofacial Primary Cutaneous Actinomycosis; Cutaneous actinomycosis; Leptotrichosis; Lumpy Jaw; primary cutaneous actinomycosis; Radiation fungal disease; Streptotrichosis

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

HistoryThis section has been translated automatically.

Israel 1878; Bollinger 1877

DefinitionThis section has been translated automatically.

Globally occurring, rare (constantly decreasing in industrialized countries), endogenous (mostly after dental surgery), bacterial (mixed) infectious disease caused by a facultative pathogen (Actinomyces israelii) occurring in the physiological oral cavity flora which causes the infection in connection with symbiotic accompanying bacteria.

PathogenThis section has been translated automatically.

Anaerobic, Gram-positive and Grocott-positive pathogens, mainly Actinomyces israelii, less frequently Actinomyces naeslundi and Actinomyces radingae; Actinomyces bovi also occurs in individual cases in humans. Always mixed infection(staphylococci, streptococci, Pseudomonas aeruginosa, fusobacteria, etc.). Actinomyces israelii is a germ of the normal flora of humans and animals and occurs mainly in the mouth and throat.

ClassificationThis section has been translated automatically.

According to the localization of the manifestations 3 forms are distinguished:

  • Cervicofacial actinomycosis: about 80-85% of all cases.
  • Thoracic actinomycosis: about 13-15% of all cases.
  • Abdominal actinomycosis: about 3% of all cases
  • Other (see casuistry)

Occurrence/EpidemiologyThis section has been translated automatically.

Worldwide appearance. It occurs more frequently among the rural population than among the urban population. More common in developing countries, but very rare in industrialized countries due to the more frequent use of antibiotics.

m:w=3:1;

ManifestationThis section has been translated automatically.

Especially 20-40. LJ.

LocalizationThis section has been translated automatically.

Mostly in the soft tissues of the face and neck region (cervico-facial form); also thorax (thoracic form), abdomen (abdominal form), arms or buttocks.

Clinical featuresThis section has been translated automatically.

incubation period: about 4 weeks

The infection often spreads from the depth of the lower jaws to the skin. Fever and local pain can be accompanying symptoms.

On the skin (more rarely on the mucous membrane: macroglossia) and the deep tissue there are hard, blue-red, infiltrated indurations and nodules with a tendency to ulceration or melting with a tendency to fistulas and pronounced scarring. Often adhesions in the surrounding tissue. In the exiting pus macroscopically recognizable, 0.2-0.5 cm large, irregularly shaped, yellowish, solid grains ( drusen) can already be seen. No spontaneous healing tendency.

HistologyThis section has been translated automatically.

Non-specific granulation tissue with eosinophil granulocytes or plasma cells. Partially leukocyte-rich fusion necroses. The granules (drusen), which are almost pathognomic for actinomycosis, can be detected in melting abscesses also in HE section. The individual actinomycetes are sintered together in the centre, where they are not recognisable as individual elements. Only in the periphery are individual, thread-like structures detectable. In addition to the HE staining, the Grocott method is recommended for the visualisation of the drusen.

DiagnosisThis section has been translated automatically.

Clinic, histology from a deep excision biopsy (punch biopsies are not sufficient with regard to their depth), detection of drusen in smears from fistula ladder in Gram staining, cultivation of the pathogen from smears or from biopsy and resistogram (increasing antibiotic resistance!), detection of the pathogen by PCR.

Differential diagnosisThis section has been translated automatically.

tuberculous abscesses

syphilitic gums

chronic pyoderma

dentogenic fistulas

osteomyelitis

oral phlegmon.

If located on the buttocks: acne conglobata or hidradenitis suppurativa

Lymphogranuloma venereum

Complication(s)This section has been translated automatically.

Oral floor phlegmon, lockjaw. Miliary seeding can occur in rare cases.

TherapyThis section has been translated automatically.

Combination of surgical and chemotherapeutic procedures.

Internal therapyThis section has been translated automatically.

Antibiotic therapy for weeks or months.

  • The drug of first choice is penicillin G: benzylpenicillin (e.g. penicillin Grünenthal) initially as a short infusion twice a day 10 million IU i.v. over at least 4-6 weeks. Then phenoxypenicillin (e.g. Baycillin Mega) 2-5 million IU/day p.o. over 4-6 months or benzathine penicillin (e.g. Tardocillin 1200), 2 ampoules i.m. every 4 weeks.
  • Alternatively ampicillin (e.g. Binotal) 4 times/day 0.5-1.0 g p.o. or 100-150 mg/kg bw/day i.v. over at least 4-6 weeks.
  • Alternative: Cephalosporin for parenteral application is especially recommended Cefoxitin (e.g. Mefoxitin) 3-4 times/day 1.0-2.0 g i.v. because of its broad spectrum and the special anaerobic component.
  • Alternatively: Tetracycline (e.g. Tetracycline-ratiopharm) 3-4 times/day 0.5 g p.o. over 4-6 weeks or Lincomycin (e.g. Albiotic) 3-4 times/day 500 mg p.o. or 3-4 times/day 600 mg/day i.v.
  • In case of mixed infections with staphylococci or other anaerobes, flucloxacillin (e.g. Staphylex Kps.) is additionally applied 3-4 times/day 0.5-1.0 g p.o., i.m. or i.v. Alternatively, clindamycin (e.g. sobelin) can be applied 3-4 times/day 300 mg p.o. or 3-4 times/day 600 mg i.v.
  • In case of resistance to therapy, it is recommended to cultivate the pathogen and to treat it with resistogram-adapted therapy.

Operative therapieThis section has been translated automatically.

Incision and drainage of abscesses, excision of chronic fibrotic tissue that is not supplied with blood.

Progression/forecastThis section has been translated automatically.

Highly chronic course; no impairment of the general condition; however, the board-like infiltrates and osteomyelitis lead to retracted and disfiguring scars. Cervical actinomycosis has a favourable prognosis if diagnosed in time and treated sufficiently (Jeong YJ et al. 2017).

Case report(s)This section has been translated automatically.

In a 44-year-old patient a largely symptom-free, 3x2cm red, exulcerated induration developed on the outside of the right upper arm after a slight dog bite for more than half a year. In the course of this time a nodular size progression occurred, with increasing ulceration and constant purulent secretion. An analogous focal point appeared on the left (!) arm. Laboratory examination revealed leukocytosis (11,500/ml), as well as increased inflammatory parameters (BSG: 35/h; CRP:5.2mg/dl). A peroral antibiotic therapy with clindamycin did not show any improvement. A deep excision biopsy revealed deep granulation tissue with neutrophil abscesses. No evidence of drusen. However, a microbiological examination of the tissue carried out at the same time led to the detection of Actinomyces naeslundi. The germ was resistant to clindamycin. The antibiotic therapy was changed to a combination treatment with moxifloxacin and ampicillin/sulbactam. Including healing of the findings after 6 weeks.

LiteratureThis section has been translated automatically.

  1. Charalabopoulos K et al (2003) Lung, pleural and colon actinomycosis in an immunocompromised patient: a rare form of presentation. Chemotherapy 49: 209-211
  2. Chaudhry SI, Greenspan JS (2000) Actinomycosis in HIV infection: a review of a rare complication. Int J STD AIDS 11: 349-355
  3. Clarridge JE 3rd, Zhang Q (2002) Genotypic diversity of clinical Actinomyces species: phenotype, source, and disease correlation among genospecies. J Clin Microbiol 40: 3442-3448.
  4. Cocuroccia B et al (2003) Primary cutaneous actinomycosis of the forehead. J Eur Acad Dermatol Venereol 17: 331-333.
  5. Israel JA (1885) Clinical contributions to the knowledge of actinomycosis of man. A. Hirschwald (Berlin), pp 152.
  6. Israel JA (1885) Clinical contributions to the knowledge of actinomycosis of man. Z Clin Med 6: 392
  7. Jeong YJ et al (2017) Cervicofacial primary cutaneous actinomycosis: Surgical Treatment for Complete Remission of the Disease. J Craniofac Surg 28:e269-e271.
  8. Khadka P et al (2019) Primary cutaneous actinomycosis: a diagnostic consideration in people living with HIV/AIDS. AIDS Res Ther 16:16.

  9. Kobayashi KI et al.(2019) Erysipelothrix rhusiopathiae bacteremia following a cat bite.
    IDCases 18:e00631.
  10. Kodali U et al. (2003) Abdominal actinomycosis presenting as lower gastrointestinal bleeding. Endoscopy 35: 451-453
  11. Olson JM et al (2013) Primary cutaneous Actinomyces neuii infection of the breast successfully treated with doxycycline. Cutis 92:E3-E4
  12. Park JK et al (2003) Cervicofacial actinomycosis: CT and MR imaging findings in seven patients. AJNR Am J Neuroradiol 24: 331-335.
  13. Tedeschi A et al (2003) A case of pelvic actinomycosis presenting as cutaneous fistula. Eur J Obstet Gynecol Reprod Biol 108: 103-105.
  14. Varga R et al (2012) Primary cutaneous actinomycosis of the femorogluteal region: two case reports. Acta Derm Venereol 92:445-446

Authors

Last updated on: 15.06.2022