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2.
J Am Acad Dermatol ; 86(1): 113-121, 2022 01.
Article in English | MEDLINE | ID: covidwho-1401554

ABSTRACT

BACKGROUND: Cutaneous reactions after COVID-19 vaccination have been commonly reported; however, histopathologic features and clinical correlations have not been well characterized. METHODS: We evaluated for a history of skin biopsy all reports of reactions associated with COVID-19 vaccination identified in an international registry. When histopathology reports were available, we categorized them by reaction patterns. RESULTS: Of 803 vaccine reactions reported, 58 (7%) cases had biopsy reports available for review. The most common histopathologic reaction pattern was spongiotic dermatitis, which clinically ranged from robust papules with overlying crust, to pityriasis rosea-like eruptions, to pink papules with fine scale. We propose the acronym "V-REPP" (vaccine-related eruption of papules and plaques) for this spectrum. Other clinical patterns included bullous pemphigoid-like (n = 12), dermal hypersensitivity (n = 4), herpes zoster (n = 4), lichen planus-like (n = 4), pernio (n = 3), urticarial (n = 2), neutrophilic dermatosis (n = 2), leukocytoclastic vasculitis (n = 2), morbilliform (n = 2), delayed large local reactions (n = 2), erythromelalgia (n = 1), and other (n = 5). LIMITATIONS: Cases in which histopathology was available represented a minority of registry entries. Analysis of registry data cannot measure incidence. CONCLUSION: Clinical and histopathologic correlation allowed for categorization of cutaneous reactions to the COVID-19 vaccine. We propose defining a subset of vaccine-related eruption of papules and plaques, as well as 12 other patterns, following COVID-19 vaccination.


Subject(s)
COVID-19 Vaccines/adverse effects , COVID-19 , Exanthema , Skin Diseases/chemically induced , COVID-19/prevention & control , Exanthema/chemically induced , Humans , Registries
3.
Clin Appl Thromb Hemost ; 26: 1076029620943671, 2020.
Article in English | MEDLINE | ID: covidwho-676150

ABSTRACT

Severe acute respiratory syndrome coronavirus 2 infection (COVID-19) is known to induce severe inflammation and activation of the coagulation system, resulting in a prothrombotic state. Although inflammatory conditions and organ-specific diseases have been shown to be strong determinants of morbidity and mortality in patients with COVID-19, it is unclear whether preexisting differences in coagulation impact the severity of COVID-19. African Americans have higher rates of COVID-19 infection and disease-related morbidity and mortality. Moreover, African Americans are known to be at a higher risk for thrombotic events due to both biological and socioeconomic factors. In this review, we explore whether differences in baseline coagulation status and medical management of coagulation play an important role in COVID-19 disease severity and contribute to racial disparity trends within COVID-19.


Subject(s)
Betacoronavirus , Black or African American , Coronavirus Infections/ethnology , Pandemics , Pneumonia, Viral/ethnology , Thrombophilia/ethnology , Venous Thromboembolism/ethnology , Black or African American/genetics , Anemia, Sickle Cell/blood , Anemia, Sickle Cell/ethnology , Anticoagulants/therapeutic use , Blood Proteins/analysis , Blood Proteins/genetics , COVID-19 , Clinical Trials as Topic , Comorbidity , Coronavirus Infections/blood , Coronavirus Infections/complications , Factor VIII/analysis , Female , Fibrin Fibrinogen Degradation Products/analysis , Genetic Association Studies , Genetic Predisposition to Disease , Healthcare Disparities , Humans , Lupus Erythematosus, Systemic/blood , Lupus Erythematosus, Systemic/ethnology , Male , Patient Selection , Pneumonia, Viral/blood , Pneumonia, Viral/complications , Polymorphism, Single Nucleotide , Prevalence , Renal Insufficiency, Chronic/blood , Renal Insufficiency, Chronic/ethnology , Risk Factors , SARS-CoV-2 , Social Determinants of Health , Socioeconomic Factors , Thrombophilia/blood , Thrombophilia/drug therapy , Thrombophilia/etiology , Venous Thromboembolism/blood , Venous Thromboembolism/etiology , Venous Thromboembolism/prevention & control
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