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Published on: July 15, 2019
Atypical hand, foot and mouth disease in adults associated with coxsackievirus A6: a clinico-pathologic study
Alvaro C Laga1, Suzanne M Shroba2, John Hanna3
1Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA. alaga@partners.org.
Insights
Atypical hand, foot, and mouth disease (HFMD) in adults, caused by Coxsackievirus A6, presents challenging skin symptoms. Early recognition of this uncommon HFMD variant is crucial for correct diagnosis and prognosis.
Area of Science:
- Dermatology
- Virology
- Infectious Diseases
Background:
- Hand, foot, and mouth disease (HFMD) is typically a childhood illness caused by Coxsackievirus A16.
- Adult cases are rare and can exhibit atypical, severe skin manifestations.
Observation:
- Three adult cases of atypical HFMD were analyzed for clinical, histopathologic, and molecular features.
- Clinical presentation mimicked erythema multiforme or herpesvirus infection.
- Histopathology revealed intraepidermal vesiculation with neutrophil infiltrate, affecting specific skin layers.
Findings:
- Molecular analysis identified Coxsackievirus A6 in two cases, an uncommon HFMD serotype.
- No evidence of herpesvirus was found in any case.
- All three patients experienced spontaneous resolution of symptoms.
Implications:
- Atypical HFMD due to Coxsackievirus A6 is a rare but diagnostically challenging condition.
- Accurate identification is vital to prevent unnecessary treatments and set appropriate patient expectations.
- Understanding atypical HFMD presentations improves clinical management and diagnostic accuracy.
Background:
Hand, foot, and mouth disease (HFMD) is a contagious illness most commonly occurring in children 5 years old or younger. The most common cause of HFMD in the United States is Coxsackievirus A16. HFMD is uncommon in adults, and may show other atypical features including a broader spectrum of cutaneous involvement and a greater degree of severity.
Methods:
We evaluated the clinical, histopathologic and molecular features of three cases of atypical HFMD occurring in adults.
Results:
All three cases showed clinical features that were worrisome for erythema multiforme or a disseminated herpesvirus infection. The histopathologic findings were quite uniform, and showed intraepidermal vesiculation with a predominantly neutrophil-rich infiltrate. A characteristic feature was the specific involvement of the upper stratum spinosum and stratum granulosum, with relative sparing of the stratum corneum. In none of the cases was there evidence of herpesvirus. Molecular analysis performed on two of the cases showed involvement by Coxsackievirus A6, an uncommon serotype in HFMD. All three cases resolved spontaneously.
Conclusions:
Atypical HFMD associated with Coxsackievirus A6 represents an uncommon and potentially diagnostically challenging cutaneous eruption. Its recognition is critical to avoid unneeded therapy and to establish accurate prognostic expectations.
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