Ecthyma

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Background

Ecthyma is an ulcerative pyoderma of the skin well known to be caused by group A beta-hemolytic streptococci. Concomitant Staphylococcus aureus is often isolated from lesional skin.[1] On occasion, S aureus alone has been isolated.[2] Because ecthyma extends into the dermis, it is often referred to as a deeper form of impetigo.



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Typical ecthyma lesions of the lower extremities.



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The stages of ecthyma: the lesion begins as a pustule that later erodes and ultimately forms an ulcer with adherent crust.

Pathophysiology

Ecthyma begins similarly to superficial impetigo. Group A beta-hemolytic streptococci may initiate the lesion or may secondarily infect preexisting wounds. Preexisting tissue damage (eg, excoriations, insect bites, dermatitis) and immunocompromised states (eg, diabetes, neutropenia) predispose patients to the development of ecthyma. Spread of skin streptococci is augmented by crowding and poor hygiene.

Etiology

Ecthyma can be seen in areas of previously sustained tissue injury (eg, excoriations, insect bites, dermatitis). Insect bites in the setting of recent travel have been associated with ecthyma.[2]

Ecthyma can be seen in patients who are immunocompromised (eg, diabetes, neutropenia, HIV infection).[3]

Important factors that contribute to the development of streptococcal pyodermas or ecthyma include the following:

Untreated impetigo that progresses to ecthyma most frequently occurs in patients with poor hygiene.

Some strains of Streptococcus pyogenes have a high affinity for both pharyngeal mucosa and skin. Pharyngeal colonization of S pyogenes has been documented in patients with ecthyma.[6] Ecthyma has also been reported in the setting of perianal streptococcal disease.[7]

Epidemiology

Frequency

The exact incidence of ecthyma worldwide remains unknown.

Race

No racial predisposition is recognized for ecthyma.

Sex

No sexual predisposition is recognized for ecthyma.

Age

Ecthyma has a predilection for children and elderly individuals. Outbreaks have also been reported in young military trainees.[6]

Prognosis

Ecthyma lesions are slow to heal but do respond to appropriate antibiotics and local wound care; prognosis is favorable.

Ecthyma rarely leads to systemic symptoms or bacteremia. Lesions are painful and can have associated lymphadenopathy. Secondary lymphangitis and cellulitis, as well as poststreptococcal glomerulonephritis, can occur. Ecthyma does heal with scarring.

Patient Education

For patient education resources, see the Skin Conditions and Beauty Center. Also, see the patient education article Impetigo.

History

Ecthyma usually arises on the lower extremities of children, persons with diabetes, and neglected elderly patients. During wartime in tropical climates, ecthymatous ulcers are commonly found on the ankles and dorsi of the feet.

Physical Examination

Ecthyma begins as a vesicle or pustule overlying an inflamed area of skin that deepens into a dermal ulceration with overlying crust. The crust of ecthyma lesions is gray-yellow and is thicker and harder than the crust of impetigo. A shallow, punched-out ulceration is apparent when adherent crust is removed. The deep dermal ulcer has a raised and indurated surrounding margin.

Ecthyma lesions can remain fixed in size (sometimes resolving without treatment) or can progressively enlarge to 0.5-3 cm in diameter.

Ecthyma heals slowly and commonly produces a scar.

Regional lymphadenopathy is common, even with solitary lesions.

Complications

Ecthyma rarely produces systemic symptoms.

Invasive complications of streptococcal skin infections include cellulitis, erysipelas, gangrene, lymphangitis, suppurative lymphadenitis,[8] bursitis,[6] lobar pneumonia,[6] and bacteremia.

Nonsuppurative complications of streptococcal skin infections include scarlet fever and acute glomerulonephritis. Prompt antibiotic therapy does not appear to reduce the rate of poststreptococcal glomerulonephritis. Streptococcal toxic shock syndrome has been reported.[6]

Possible sequelae of secondary untreated S aureus pyodermas include cellulitis, lymphangitis, bacteremia, osteomyelitis, and acute infective endocarditis. Some S aureus strains produce exotoxins that can lead to staphylococcal scalded skin syndrome and toxic shock syndrome.

Laboratory Studies

Gram stain and culture of ecthyma lesions reveal gram-positive cocci that represent group A streptococci, with or without Staphylococcus aureus. Prior group A streptococci infection can be detected by anti-DNase beta testing.

Histologic Findings

Ecthyma lesions show dermal necrosis and inflammation. A deep and superficial granulomatous perivascular infiltrate occurs along with endothelial edema. A heavy crust covers the surface of the ecthyma ulcer.

Medical Care

Oral antibiotics are used to treat ecthyma. Hygiene is also important. Maintain cleanliness by using bactericidal soap and frequently changing bed linens, towels, and clothing. Remove ecthyma crusts by soaking or using wet compresses. Lesions should then be covered with petroleum jelly or mupirocin ointment.[9]

Oral penicillin is the standard of care for documented streptococcal ecthyma. Typically, a 7-day course is adequate.[10] If concomitant or primary S aureus infection is suspected, oral dicloxacillin and cephalexin are recommended as isolates are typically methicillin-susceptible.[10] Of interest, a 1971 study by Kelly et al demonstrated benzathine penicillin G eradication of streptococci and clinical healing of ecthyma lesions despite the concomitant presence of staphylococci.[1] If methicillin-resistant S aureus is isolated or suspected, doxycycline, clindamycin, and sulfamethoxazole-trimethoprim are therapeutic options.[10] Consider parenteral antibiotics for widespread ecthyma and in the setting of community outbreaks of poststreptococcal glomerulonephritis.[10]

Additional FDA-approved antibiotics for the treatment of acute bacterial skin and skin structure infections include oritavancin (Orbactiv), dalbavancin (Dalvance), and tedizolid (Sivextro). These agents are active against Staphylococcus aureus (including methicillin-susceptible and methicillin-resistant S aureus [MSSA, MRSA] isolates), Streptococcus pyogenes, Streptococcus agalactiae, and Streptococcus anginosus group (includes Streptococcus anginosus, Streptococcus intermedius, and Streptococcus constellatus), among others. For complete drug information, including dosing, see the following monographs:

 

Surgical Care

Gently debride ecthyma crusts.

Prevention

Maintaining cleanliness is critical for preventing ecthyma. Using insect repellants to prevent bites also may decrease the prevalence of ecthyma.

Guidelines Summary

The Infectious Diseases Society of America recently updated their guidelines for the diagnosis and management of skin and soft tissue infections. For the full guidelines, see Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America.[10, 11]

Medication Summary

The goals of pharmacotherapy for ecthyma are to reduce morbidity and to prevent complications.

Penicillin G benzathine (Bicillin LA)

Clinical Context:  Penicillin G benzathine is the drug of choice when a pyoderma is known to be caused by group A streptococci. It interferes with the synthesis of cell wall mucopeptides during active multiplication, which results in bactericidal activity.

Penicillin VK (Veetids, Beepen-VK)

Clinical Context:  Penicillin VK inhibits biosynthesis of cell wall mucopeptide and is effective during the stage of active multiplication. Inadequate concentrations may produce only bacteriostatic effects.

Cephalexin (Keflex, Biocef)

Clinical Context:  Cephalexin is a first-generation cephalosporin that arrests bacterial growth by inhibiting bacterial cell wall synthesis. It has bactericidal activity against rapidly growing organisms. Its primary activity is against skin flora; it is used for skin infections or prophylaxis in minor procedures. It is active against Streptococcus pyogenes and S aureus.

Dicloxacillin (Dycill, Dynapen)

Clinical Context:  Dicloxacillin is used for treatment of infections caused by penicillinase-producing staphylococci. It can be used to initiate therapy when staphylococcal infection is suggested.

Clindamycin (Cleocin)

Clinical Context:  Clindamycin is a lincosamide for the treatment of serious skin and soft-tissue staphylococcal infections. It is also effective against aerobic and anaerobic streptococci (except enterococci). It inhibits bacterial growth, possibly by blocking dissociation of peptidyl t-RNA from ribosomes, causing RNA-dependent protein synthesis to arrest.

Trimethoprim/sulfamethoxazole (Bactrim, Bactrim DS, Cotrim)

Clinical Context:  This combination agent inhibits the biosynthesis of proteins and nucleic acids needed for bacterial growth. It typically is effective for methicillin-resistant S aureus.

Doxycycline (Doxycin, Acticlate, Adoxa)

Clinical Context:  Doxycycline inhibits bacterial growth by inhibiting protein synthesis. It often is effective for methicillin-resistant S aureus. It is not recommended for children younger than 8 years.

Mupirocin (Bactroban)

Clinical Context:  Mupirocin selectively binds to bacterial isoleucyl transfer-RNA synthetase, inhibiting protein synthesis.

Class Summary

Topical antibiotics should be considered adjunctive therapy in addition to systemic antibiotics for the treatment of ecthyma.

Author

Loretta S Davis, MD, Professor and Chair, Department of Dermatology, Medical College of Georgia, Augusta University

Disclosure: Nothing to disclose.

Specialty Editors

David F Butler, MD, Former Section Chief of Dermatology, Central Texas Veterans Healthcare System; Professor of Dermatology, Texas A&M University College of Medicine; Founding Chair, Department of Dermatology, Scott and White Clinic

Disclosure: Nothing to disclose.

Lester F Libow, MD, Dermatopathologist, South Texas Dermatopathology Laboratory

Disclosure: Nothing to disclose.

Chief Editor

William D James, MD, Paul R Gross Professor of Dermatology, Vice-Chairman, Residency Program Director, Department of Dermatology, University of Pennsylvania School of Medicine

Disclosure: Received income in an amount equal to or greater than $250 from: Elsevier; WebMD.

Additional Contributors

Donald Belsito, MD, Professor of Clinical Dermatology, Department of Dermatology, Columbia University Medical Center

Disclosure: Nothing to disclose.

Acknowledgements

The authors and editors of Medscape Reference gratefully acknowledge the contributions of previous author, Carmen Mays, MD, to the development and writing of this article.

References

  1. Kelly C, Taplin D, Allen AM. Streptococcal ecthyma. Treatment with benzathine pencillin G. Arch Dermatol. 1971 Mar. 103(3):306-10. [View Abstract]
  2. Hochedez P, Canestri A, Lecso M, Valin N, Bricaire F, Caumes E. Skin and soft tissue infections in returning travelers. Am J Trop Med Hyg. 2009 Mar. 80 (3):431-4. [View Abstract]
  3. Ko WT, Adal KA, Tomecki KJ. Infectious diseases. Med Clin North Am. 1998 Sep. 82(5):1001-31, v. [View Abstract]
  4. Singh G. Heat, humidity and pyodermas. Dermatologica. 1973. 147(5):342-7. [View Abstract]
  5. Allen AM, Taplin D, Twigg L. Cutaneous streptococcal infections in Vietnam. Arch Dermatol. 1971 Sep. 104(3):271-80. [View Abstract]
  6. Wasserzug O, Valinsky L, Klement E, et al. A cluster of ecthyma outbreaks caused by a single clone of invasive and highly infective Streptococcus pyogenes. Clin Infect Dis. 2009 May 1. 48(9):1213-9. [View Abstract]
  7. Gunawardane ND, Laumann A. An immunocompromised patient with recent-onset skin lesions. JAMA. 2014 Mar 5. 311 (9):957-8. [View Abstract]
  8. Duve S, Voack C, Rakoski J, Hoffmann H. Extensive inguinal lymphadenitis. Ecthyma with inguinal lymphadenitis. Arch Dermatol. 1996 Jul. 132(7):823, 826. [View Abstract]
  9. Dagan R, Bar-David Y. Double-blind study comparing erythromycin and mupirocin for treatment of impetigo in children: implications of a high prevalence of erythromycin-resistant Staphylococcus aureus strains. Antimicrob Agents Chemother. 1992 Feb. 36(2):287-90. [View Abstract]
  10. [Guideline] Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the infectious diseases society of america. Clin Infect Dis. 2014 Jul 15. 59(2):e10-52. [View Abstract]
  11. Barclay L. IDSA: skin and soft tissue infections guidelines updated. Medscape Medical News. Available at http://www.medscape.com/viewarticle/827399. Accessed: June 26, 2014.

Typical ecthyma lesions of the lower extremities.

The stages of ecthyma: the lesion begins as a pustule that later erodes and ultimately forms an ulcer with adherent crust.

Typical ecthyma lesions of the lower extremities.

The stages of ecthyma: the lesion begins as a pustule that later erodes and ultimately forms an ulcer with adherent crust.