Literature DB >> 34713472

Leukocytoclastic vasculitis after coronavirus disease 2019 vaccination.

Woo Jung Jin1, Sang Woo Ahn1, Seung Hee Jang1, Seong Min Hong1, Jung Eun Seol1, Hyojin Kim1.   

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Year:  2021        PMID: 34713472      PMCID: PMC8652425          DOI: 10.1111/1346-8138.16212

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   3.468


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CONFLICT OF INTEREST

None declared. Dear Editor, The ChAdOx1 nCoV‐19 vaccine (AstraZeneca®; UK) has been administrated against severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). Injection‐site skin reaction has been reported as a common adverse drug reaction; however, there has been only one report of vasculitis so far with the ChAdOx1 nCoV‐19 vaccine. Herein, we present a case of new‐onset leukocytoclastic vasculitis following ChAdOx1 nCoV‐19 vaccination. A 68‐year‐old Korean woman presented with asymptomatic erythematous to purpuric non‐blanching macules on both lower extremities for 2 days (Figure 1a,b). Concomitant symptoms including fever, arthralgia, abdominal pain, or hematuria were denied. She had received the first vaccination of ChAdOx1 nCoV‐19 7 days prior to the onset of lesions. She denied any medical history, including vasculitis or medication. Laboratory finding revealed decreased C3 and C4 levels (68.3 and 2.4 mg/dL, respectively), but all other tests, including complete blood count, renal function test, urinalysis, and antinuclear antibody, were unremarkable. Histopathological examination showed perivascular and interstitial inflammatory infiltration with lymphocytes, neutrophils, eosinophils, and leukocytoclasia, with extravasation of a few erythrocytes (Figure 1c,d). She was treated with oral methylprednisolone (4 mg/day for 1 week, followed by 2 mg/day for 2 weeks), colchicine 1.2 mg/day, and topical methylprednisolone for 3 weeks. The lesions resolved and did not relapse after cessation of treatment. The lesion slightly recurred on the legs with the second vaccination, but resolved spontaneously in a few days.
FIGURE 1

(a) Clinical manifestation presented as erythematous to purpuric non‐blanching macules on both lower legs. (b) Closer image of the lesion. (c) Histopathological findings of the perivascular and interstitial inflammatory cell infiltration in superficial to mid‐dermis (hematoxylin–eosin [HE], original magnification ×100). (d) Higher magnification image showing infiltration of lymphocytes with several neutrophils and eosinophils, accompanying leukocytoclasia, endothelial cell swelling, and sparse extravasation of erythrocyte (HE, ×200)

(a) Clinical manifestation presented as erythematous to purpuric non‐blanching macules on both lower legs. (b) Closer image of the lesion. (c) Histopathological findings of the perivascular and interstitial inflammatory cell infiltration in superficial to mid‐dermis (hematoxylin–eosin [HE], original magnification ×100). (d) Higher magnification image showing infiltration of lymphocytes with several neutrophils and eosinophils, accompanying leukocytoclasia, endothelial cell swelling, and sparse extravasation of erythrocyte (HE, ×200) Polymorphic dermatological manifestations have been reported in coronavirus disease 2019 (COVID‐19) patients. Giovanni et al. classified COVID‐19‐associated cutaneous manifestations into six clinical patterns, among which purpuric vasculitic patterns represented 7.1–15.4%. Histopathological findings of vasculitic lesions vary, including leukocytoclastic vasculitis, perivascular neutrophilic and lymphocytic infiltration, fibrin deposition, or endothelial swelling. Meanwhile, correlation with immunoglobulin A vasculitis has been described in case systemic manifestations were accompanied or skin lesions were distributed to extensive area of the body. The SARS‐CoV‐2 spike protein, which is a major component of the vaccine, has been suggested to activate alternative complement pathway through binding to mannose‐binding lectin. Similar to complement‐mediated endotheliopathy in COVID‐19 patients, the SARS‐CoV‐2 spike protein may have induced complement activation or autoimmunity, thereby leading to the inflammation of the cutaneous microvasculature. Unlike the case of cutaneous vasculitis after other COVID‐19 vaccinations such as BNT162b2 (Pfizer®; USA), the decreased C3 and C4 levels in our patient reveal a clearer association between vascular injury and complement activation. The different characteristics of vaccines, including gene delivery mechanism or adjuvants, might cause variable manifestations of post‐vaccination vasculitis. Lower level of viral antigen load in vaccination compared to COVID‐19 might have contributed to favorable and self‐limiting prognosis of vasculitis, indicating that the triggering factor of the skin lesion resolved in a short period of time. Vasculitis may not be considered as a contraindication of vaccination, as it appears to occur in very exceptional cases and shows favorable prognosis. Nonetheless, clinicians should monitor cutaneous adverse reactions by vaccines. Further investigations would be necessary to clarify the characteristics of vasculitis following COVID‐19 vaccination.
  5 in total

Review 1.  Skin Manifestations Associated with COVID-19: Current Knowledge and Future Perspectives.

Authors:  Giovanni Genovese; Chiara Moltrasio; Emilio Berti; Angelo Valerio Marzano
Journal:  Dermatology       Date:  2020-11-24       Impact factor: 5.366

2.  Leukocytoclastic Vasculitis After Vaccination With a SARS-CoV-2 Vaccine.

Authors:  Anne Erler; John Fiedler; Anna Koch; Frank Heldmann; Alexander Schütz
Journal:  Arthritis Rheumatol       Date:  2021-11-29       Impact factor: 15.483

3.  Small-vessel vasculitis following Oxford-AstraZeneca vaccination against SARS-CoV-2.

Authors:  L Guzmán-Pérez; M Puerta-Peña; D Falkenhain-López; J Montero-Menárguez; C Gutiérrez-Collar; J L Rodríguez-Peralto; J Sanz-Bueno
Journal:  J Eur Acad Dermatol Venereol       Date:  2021-08-04       Impact factor: 9.228

4.  Direct activation of the alternative complement pathway by SARS-CoV-2 spike proteins is blocked by factor D inhibition.

Authors:  Jia Yu; Xuan Yuan; Hang Chen; Shruti Chaturvedi; Evan M Braunstein; Robert A Brodsky
Journal:  Blood       Date:  2020-10-29       Impact factor: 25.476

5.  Possible association between IgA vasculitis and COVID-19.

Authors:  Sunmeet Sandhu; Satish Chand; Anuj Bhatnagar; Rajeshwari Dabas; Showkat Bhat; Harish Kumar; Prashant Kumar Dixit
Journal:  Dermatol Ther       Date:  2020-11-25       Impact factor: 3.858

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Review 1.  SARS-CoV-2 vaccination-induced cutaneous vasculitis: Report of two new cases and literature review.

Authors:  Ayman Abdelmaksoud; Uwe Wollina; Selami Aykut Temiz; Abdulkarim Hasan
Journal:  Dermatol Ther       Date:  2022-03-25       Impact factor: 3.858

Review 2.  SARS-CoV-2 vaccine-related cutaneous manifestations: a systematic review.

Authors:  Gianluca Avallone; Pietro Quaglino; Francesco Cavallo; Gabriele Roccuzzo; Simone Ribero; Iris Zalaudek; Claudio Conforti
Journal:  Int J Dermatol       Date:  2022-02-09       Impact factor: 3.204

Review 3.  Autoimmune and autoinflammatory conditions after COVID-19 vaccination. New case reports and updated literature review.

Authors:  Yhojan Rodríguez; Manuel Rojas; Santiago Beltrán; Fernando Polo; Laura Camacho-Domínguez; Samuel David Morales; M Eric Gershwin; Juan-Manuel Anaya
Journal:  J Autoimmun       Date:  2022-08-24       Impact factor: 14.511

Review 4.  Cutaneous vasculitis and vasculopathy in the era of COVID-19 pandemic.

Authors:  Carlo Alberto Maronese; Enrico Zelin; Gianluca Avallone; Chiara Moltrasio; Maurizio Romagnuolo; Simone Ribero; Pietro Quaglino; Angelo Valerio Marzano
Journal:  Front Med (Lausanne)       Date:  2022-08-23
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