Literature DB >> 35491547

Oral and dermatologic lesions observed in mild COVID-19 patients infected after 3rd vaccine dose.

Lucas Alves da Mota Santana1, Gabriela Araújo da Costa2, Rani Iani Costa Gonçalo3, Wilton Mitsunari Takeshita1, Lucyene Miguita4.   

Abstract

Entities:  

Keywords:  COVID-19; SARS-CoV-2; immune response; oral cavity; vaccine

Year:  2022        PMID: 35491547      PMCID: PMC9348181          DOI: 10.1111/odi.14232

Source DB:  PubMed          Journal:  Oral Dis        ISSN: 1354-523X            Impact factor:   4.068


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AUTHOR CONTRIBUTIONS

Lucas Alves da Mota Santana: Conceptualization; Data curation; Formal analysis; Investigation; Methodology; Writing – original draft. Gabriela Araújo da Costa: Data curation; Investigation; Writing – original draft. Rani Iani Costa Gonçalo: Data curation; Formal analysis; Investigation; Methodology; Writing – original draft. Wilton Mitsunari Takeshita: Supervision; Validation; Visualization; Writing – review & editing. Lucyene Miguita: Supervision; Validation; Visualization; Writing – review & editing.

PEER REVIEW

The peer review history for this article is available at https://publons.com/publon/10.1111/odi.14232.

CONFLICTS OF INTEREST

None.

ETHICAL APPROVAL

None required. Dear Editor, During the COVID‐19 era, several cases of oral lesions associated with the novel coronavirus infection have been reported, beyond those caused secondarily after application of the vaccine as a result of immune response (Amorim Dos Santos et al., 2021; Troeltzsch et al., 2021). Despite satisfactory results, no immunizer is completely effective against new variants of SARS‐CoV‐2 infection. In addition, it is expected that vaccines protection could be compromised due to the fast‐spreading of the Omicron variant (B.1.1.529) and its large number of mutations in the spike protein. Here, we report the occurrence of oral and dermal lesions in COVID‐19 patients infected after a complete vaccination schedule, including the booster dose. In January 2022, three members of the same family tested positive for SARS‐CoV‐2, confirmed through the RT‐PCR test. In general, the symptoms were mild, with the predominance of persistent cough, headache, sore throat, and sneezing (Table S1). Myalgia, anosmia, ageusia, and fever was also reported by at least one of the patients. It was prescribed azithromycin 500 mg, dipyrone 500 mg, and prednisolone 20 mg for 5 days and monitored under home quarantine for 10 days. Curiously, 8 days following the onset of COVID‐19 symptoms, the patients showed alterations in the tongue dorsum, with papillary inflammation, foci of depapillation, and fissures. Herpetic eruptions in the neck and petechiae scattered on the dorsum and trunk were also observed in the female and one male, respectively (Figure 1).
FIGURE 1

Aspects of oral lesions and dermatologic alterations observed in patients with COVID‐19 after 3rd vaccine dose. (a) Presence of petechiae and urticaria scattered throughout the dorsal region; (b) Transient U‐shaped anterior lingual papillitis (head arrow); (c) Reduction of inflammation of the papillae's tongue (30 days after initial infection); (d) Vesiculobullous lesions of herpetic origin in neck, isolated (black arrows) and clustered (circle); (e) Focal papillitis in the anterior region of the tongue and areas of depapilation (black arrows); (f) Discreet reduction focal papillitis and absence of areas of depapilation (30 days after initial infection); (g) Fissures presence in tongue dorsum (black arrows); (h) Absence of fissures and reduction of the inflammation of the papillae's tongue (30 days after initial infection)

Aspects of oral lesions and dermatologic alterations observed in patients with COVID‐19 after 3rd vaccine dose. (a) Presence of petechiae and urticaria scattered throughout the dorsal region; (b) Transient U‐shaped anterior lingual papillitis (head arrow); (c) Reduction of inflammation of the papillae's tongue (30 days after initial infection); (d) Vesiculobullous lesions of herpetic origin in neck, isolated (black arrows) and clustered (circle); (e) Focal papillitis in the anterior region of the tongue and areas of depapilation (black arrows); (f) Discreet reduction focal papillitis and absence of areas of depapilation (30 days after initial infection); (g) Fissures presence in tongue dorsum (black arrows); (h) Absence of fissures and reduction of the inflammation of the papillae's tongue (30 days after initial infection) Although less frequently reported than cutaneous lesions, oral manifestations associated with COVID‐19 include dry mouth, ulcers, oral vesiculobullous lesions, and tongue alterations (Martín Carreras‐Presas et al., 2021; Nuño González et al., 2021). Regarding these alterations, some authors have postulated the likelihood of associated infections, with SARS‐CoV‐2 possibly being the trigger for the appearance of opportunistic infections (de Carvalho et al., 2021). Particularly, we do not discard the hypothesis of occurrence of the co‐infections, such as described here. The symptoms remission did not allow enough time to conduct specific tests due to treatment effectiveness. However, the presence of a skin vesiculobullous lesion in one of the patients with a previous medical history of Herpes simplex with exacerbation after COVID‐19 infection points to the likelihood of co‐infection. In this study conducted by Nuño González et al. (2021), they have found that 25.7% of the 666 COVID‐19 patients investigated had oral manifestations, and 3.9% of them presented U form depapillation areas named “COVID tongue.” This is probably caused by the SARS‐CoV‐2 linkage for ACE‐2 receptors present on the epithelial cell of the tongue dorsum (Marques et al., 2021). Nevertheless, the presence of the virus can cause cytological alterations in these cells, especially the reduction of cellular and nuclear diameters (Marques et al., 2021). Immunologically, recurrent cases of COVID‐19 or symptom variability in the individuals may be explained by the lack of effective SARS‐CoV‐2‐specific T‐cell immune response, as observed in monozygotic twins (de Castro et al., 2022). Possibly, this mechanism may occur in vaccinated patients favoring the development of symptoms, including oral lesions, as reported here. Although most vaccines do not completely prevent infection, they do prevent the risk of aggravating a patient's health, as described in our case series. Additionally, human genomics has been considered to affect disease susceptibility and severity of COVID‐19 (Asgari & Pousaz, 2021; Hou et al., 2020). Alongside, Hou et al. (2020) found unique genetic susceptibility for COVID‐19 across different populations, specifically due to the existence of ACE2 and TMPRSS2 polymorphisms. This finding is of great clinical relevance since these polymorphisms could guide the development of effective therapies. Finally, these observations might help to understand the SARS‐CoV‐2 infection underlying mechanisms and to explain why even some fully vaccinated patients may present unexpected symptoms, including cutaneous and oral manifestations. Table S1 Click here for additional data file.
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2.  Oral Manifestations in Patients with COVID-19: A 6-Month Update.

Authors:  J Amorim Dos Santos; A G C Normando; R L Carvalho da Silva; A C Acevedo; G De Luca Canto; N Sugaya; A R Santos-Silva; E N S Guerra
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3.  Human genetic variants identified that affect COVID susceptibility and severity.

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4.  New insights into genetic susceptibility of COVID-19: an ACE2 and TMPRSS2 polymorphism analysis.

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5.  Oral lesions of herpes zoster in COVID-19 patients or truly associated to the disease?

Authors:  Luis Felipe das Chagas E Silva de Carvalho; Dárcio Kitakawa; Luiz Antônio Guimarães Cabral
Journal:  Oral Dis       Date:  2020-07-07       Impact factor: 4.068

6.  Oral vesiculobullous lesions associated with SARS-CoV-2 infection.

Authors:  Carmen Martín Carreras-Presas; Juan Amaro Sánchez; Antonio Francisco López-Sánchez; Enric Jané-Salas; Maria Luisa Somacarrera Pérez
Journal:  Oral Dis       Date:  2020-05-29       Impact factor: 4.068

7.  Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pair.

Authors:  Mateus V de Castro; Keity S Santos; Juliana S Apostolico; Edgar R Fernandes; Rafael R Almeida; Gabriel Levin; Jhosiene Y Magawa; João Paulo S Nunes; Mirian Bruni; Marcio M Yamamoto; Ariane C Lima; Monize V R Silva; Larissa R B Matos; Vivian R Coria; Erick C Castelli; Marilia O Scliar; Andreia Kuramoto; Fernanda R Bruno; Lucas C Jacintho; Kelly Nunes; Jaqueline Y T Wang; Veronica P Coelho; Miguel Mitne Neto; Rui M B Maciel; Michel S Naslavsky; Maria Rita Passos-Bueno; Silvia B Boscardin; Daniela S Rosa; Jorge Kalil; Mayana Zatz; Edecio Cunha-Neto
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8.  Morphological alterations in tongue epithelial cells infected by SARS-CoV-2: A case-control study.

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1.  New onset and exacerbation of oral lichenoid mucositis following SARS-CoV-2 infection or vaccination.

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2.  Management of oral lesions following COVID-19 vaccination.

Authors:  Betsy Joseph; Pradeep Kumar Yadalam; Raghavendra Vamsi Anegundi
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3.  Persistent erythematous candidiasis as a sequela after SARS-CoV-2 infection: A case report.

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