Pandemic coronavirus disease (Coronavirus disease 2019, [COVID‐19]) is caused by a new pathogen, severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), isolated for the first time in December 2019 in Wuhan, China. 1 The most common clinical presentation is respiratory, but other organs can also be affected, including the skin. It is estimated that approximately 20% of patients affected by COVID‐19 have skin lesions, 45% at onset and 55% during hospitalization or over the course of the disease, and there is no evidence to date that skin lesions occur by viral replication in situ. The dermatological manifestations do not seem to be related to the viral load, although acro‐ischemic lesions have been described more frequently in paucisymptomatic (oligosymptomatic) young patients. 2 , 3 There is also a relationship between some cutaneous manifestations and the overall prognosis of the patient, such as necrotic and ecchymotic forms associated with more severe disease. 4
As far as we know, there have been no descriptions of skin manifestations of COVID‐19 infection in Latin American patients; thus, we are lacking information in patients of skin of color (Fitzpatrick phototypes III‐V). The characterization of these patterns can help dermatologists and attending physicians in Latin American countries to identify paucisymptomatic patients. To fill this gap, we performed a cross‐sectional study using a questionnaire.
The Ibero‐Latin American School of Dermatology (Colegio Ibero‐Latinoamericano de Dermatología—CILAD) and the Mexican Society of Dermatology (Sociedad Mexicana de Dermatología) developed a questionnaire (Adapted from: COVID‐19 skin signs by Dr. Noufal Raboobee, available as supporting information in Spanish and Portuguese) to investigate dermatological lesions associated with COVID‐19 infection in Latin America. With this instrument, information on the dermatological phototype and preexisting dermatological conditions at the time of COVID‐19 diagnosis was obtained. Additionally, questions used to obtain the method of diagnosis, the symptomatology and treatment of COVID‐19, and a description of the associated dermatological lesions were included. The opportunity to attach photographs of these lesions was provided. This proposed questionnaire was circulated among a group of experts and then a panel was held to adapt it and their commentaries were added. The final version was uploaded to an online platform for distribution through an electronic link to all dermatological societies and the main dermatological hospitals and services in the region. The participating countries were Argentina, Bolivia, Brazil, Chile, Colombia, Costa Rica, Cuba, Ecuador, El Salvador, Granada, Guatemala, Honduras, Jamaica, Mexico, Nicaragua, Panama, Paraguay, Peru, Dominican Republic, Saint Lucia, Saint Vincent and the Grenadines, Suriname, Trinidad and Tobago, Uruguay, and Venezuela. The survey was active from June 9 to July 30, 2020. The data were evaluated through a noninferential descriptive statistical analysis. The project was approved by the Ethics Committee of the Universidad Autónoma de Nuevo León, Mexico, with the code DE20‐00005.
Although 730 questionnaires were received, only 347 were fully processed due to missing data. In this study, we found a predominance of females: 179/347. The mean age at presentation was 40.87 years, with a median of 41.0 years and a range of 7 to 90 years. In 99.4% (345/347), the Fitzpatrick phototype was reported; the most frequent was III, 45.8%; followed by IV, 39.1%; II, 13%; V, 1.7% and I, with 0.3% (Table 1).
Characteristic | Frequency (percentage) |
---|---|
Surveys (n = 730) | |
Language | |
Spanish | 670 (91.78%) |
Portuguese | 60 (8.22%) |
Origin | |
Mexico | 227 (31.1%) |
Argentina | 85 (11.6%) |
Brazil | 59 (8.1%) |
Colombia | 48 (6.6%) |
Peru | 38 (5.2%) |
Chile | 34 (4.7%) |
Ecuador | 33 (4.5%) |
Dominican Republic | 27 (3.7%) |
Venezuela | 27 (3.7%) |
Bolivia | 24 (3.3%) |
Honduras | 24(3.3%) |
Guatemala | 23 (3.2%) |
Nicaragua | 15 (2.1%) |
Paraguay | 14 (1.9%) |
No answer | 17 (2.3%) |
El Salvador | 11 (1.5%) |
Costa Rica | 9 (1.2%) |
Panama | 5 (0.7%) |
Uruguay | 4 (0.5%) |
Trinidad and Tobago | 3 (0.4%) |
Suriname | 2 (0.3%) |
Cuba | 1 (0.1%) |
Patients (n = 347) | |
Gender | |
Female | 179 (51.6%) |
Male | 168 (48.4%) |
Age | |
Mean (±standard deviation) | 40.87 (±20.47) |
Median (interquartile range) | 41.0 (28.0 – 58.0) |
Minimum–maximum | (7–90) |
Phototype (n = 345) | |
I | 1 (0.3%) |
II | 45 (13%) |
III | 158 (45.8%) |
IV | 135 (39.1%) |
V | 6 (1.7%) |
The attending physicians reported that 92.3% of patients presented signs and symptoms in the skin, hair, nails, or mucous membranes. Regarding the possible etiology of the dermatological manifestations, 82.7% of dermatologists considered these presentations likely to be related to COVID‐19, 4.3% considered them likely to be related to treatment, 1.2% said that they were likely related to a drug other than the one used for the treatment of COVID‐19, 1.7% considered them related to another virus, 4% considered them likely to be related to postviral eruption, and 2.3% were not sure. The most frequent dermatological manifestations were maculopapular rash (20.5%) and urticarial lesions (20.5%), followed by papulovesicular lesions (9.9%), vesicular lesions (7.8%), pseudo‐chilblains (7.8%), papular lesions (7.1%), ecchymosis (5%), petechial purpura (4.7%), pityriasis rosea‐like lesions (4%), pruritus (2.8%), palmoplantar dysesthesias (2.8%), transient livedo (2.2%), acral necrosis (2.2%), palpable purpura (1.6%), livedo racemosa (0.6%), and retiform purpura (0.6%). Only 15.3% of patients underwent a biopsy (Figs. 1, 2, 3 and Table 2).
Characteristics | Frequency (percentage) |
---|---|
Etiology of manifestations (n = 347) | |
Most likely related to COVID‐19 | 287 (82.7%) |
Most likely related to treatment | 15 (4.3%) |
Most likely related to a drug other than the ones used to treat COVID‐19 | 4 (1.15%) |
Most likely related to another virus | 6 (1.72%) |
Most likely related to postviral rash | 14 (4.03%) |
Not sure | 8 (2.3%) |
Did not answer | 6 (1.72%) |
Signs or symptoms (n = 322) | |
Maculopapular rash | 66 (20.5%) |
Urticarial lesions | 66 (20.5%) |
Papulovesicular lesions | 32 (9.9%) |
Vesicular lesions | 25 (7.8%) |
Chilblains | 25 (7.8%) |
Papular lesions | 23 (7.1%) |
Ecchymosis | 16 (5.0%) |
Petechial purpura | 15 (4.7%) |
Pityriasis rosea‐like lesions | 13 (4.0%) |
Pruritus | 9 (2.8%) |
Palmar or plantar dysesthesias | 9 (2.8%) |
Transient livedo | 7 (2.2%) |
Acral necrosis | 7 (2.2%) |
Palpable purpura | 5 (1.6%) |
Livedo racemosa | 2 (0.6%) |
Retiform purpura | 2 (0.6%) |
Biopsy (n = 347) | |
Yes | 53 (15.27%) |
No | 287 (82.71%) |
Not known | 1 (0.29%) |
Did not answer | 6 (1.72%) |
Preexisting dermatological diseases (n = 347) | |
Yes | 51 (14.69%) |
No | 263 (75.79%) |
Not known | 22 (6.34%) |
Did not answer | 11 (3.17%) |
Diagnostic test for COVID‐19 (n = 347) a | |
Clinical diagnosis | 87 (25.07%) |
PCR positive | 225 (64.84%) |
Positive antibodies | 50 (14.40%) |
PCR negative | 12 (3.46%) |
Negative antibodies | 1 (0.28%) |
Metagenomic test | 0 |
Not known whether a test was performed for COVID‐19 | 1 (0.28%) |
Other | 26 (7.49%) |
General symptoms (n = 347) a | |
Fever | 206 (59.37%) |
Cough | 166 (47.84%) |
Headache | 123 (35.45%) |
General malaise | 121 (34.45%) |
Respiratory distress | 97 (27.95%) |
Myalgia | 86 (24.78%) |
Odynophagia | 73 (21.04%) |
Arthralgia | 64 (18.44%) |
Diarrhea, vomiting, or nausea | 59 (17.00%) |
Anosmia | 59 (17.00%) |
Dysgeusia | 44 (12.68%) |
Chest pain | 37 (10.66%) |
None (asymptomatic) | 35 (10.09%) |
Rhinorrhea | 28 (8.07%) |
Abdominal pain | 18 (5.19%) |
Irritability/confusion | 12 (3.46%) |
Not known | 4 (1.15%) |
Other | 31 (8.93%) |
Treatment received (n = 347) a | |
Supportive care | 241 (69.45%) |
Antibiotics 1 | 168 (48.41%) |
Other 2 | 104 (29.97%) |
Glucocorticoids | 90 (25.94%) |
Ivermectin | 73 (21.04%) |
Antimalarial | 33 (9.51%) |
Not known | 13 (3.75%) |
IL‐6 inhibitors | 10 (2.88%) |
Lopinavir/ritonavir | 6 (1.73%) |
JAK inhibitors | 6 (1.73%) |
IVIG | 5 (1.44%) |
Convalescent plasma | 3 (0.86%) |
Remdesivir | 3 (0.86%) |
Ciclesonide | 2 (0.58%) |
Interferon | 0 |
Bevacizumab | 0 |
Antibiotics used (n = 347) | |
Azithromycin | 112 (32.28%) |
Clarithromycin | 5 (1.44%) |
Other | 58 (16.71%) |
Did not use | 172 (49.57%) |
Complications (n = 347) a | |
None | 234 (67.44%) |
Acute respiratory distress syndrome | 73 (21.04%) |
Sepsis | 22 (6.34%) |
Myocarditis or heart failure | 3 (0.86%) |
Concomitant lung infection or superinfection | 12 (3.46%) |
Acute kidney damage | 19 (5.48%) |
Thrombotic event | 9 (2.59%) |
It is unknown | 14 (4.03%) |
Another complication | 14 (4.03%) |
History of thrombophilia or state of hypercoagulability (n = 347) | |
Yes | 14 (4.03%) |
No | 234 (67.44%) |
Information not collected | 85 (24.50%) |
Did not answer | 14 (4.03%) |
Mortality (n = 347) | |
Yes | 46 (13.26%) |
No | 262 (75.50%) |
Not known | 15 (4.32%) |
Did not answer | 24 (6.92%) |
Regarding evidence of infection by COVID‐19, only clinical diagnosis was made in 25% of patients. The rest underwent any diagnostic test; 64.8% had a positive PCR test, 14.4% had positive antibodies, 3.5% had a negative PCR test, and 0.3% had negative antibodies; in 0.23%, it was unknown whether any type of diagnostic test was performed. No patient underwent a metagenomic test for the diagnosis of COVID‐19 infection. Only in four cases the type of diagnostic test performed was not specified. It is worth mentioning that the health professionals were able to select more than one option for this item.
The most frequently reported symptoms were as follows: fever, 59.4%; cough, 47.8%; headache, 35.5%; general malaise, 34.9%; respiratory distress, 27.95%; myalgia, 24.8%; odynophagia, 21%; arthralgia, 18.4%; diarrhea, vomiting, or nausea, 17%; anosmia, 17%; dysgeusia, 12.7%; chest pain, 10.7%; rhinorrhea, 8%; abdominal pain, 5.2%; and irritability or confusion, 3.5%. Ten percent of the cases were reported as asymptomatic. It is important to mention that the health professionals were able to select more than one option; therefore, the frequencies and percentages reflect the number of times the answer was chosen.
The treatments administered were as follows: only supportive care in 69.5% of cases, followed by antibiotics (48.4%), glucocorticoids (25.9%), ivermectin (21%), antimalarials (9.5%), IL‐6 inhibitors (2.9%), lopinavir/ritonavir (1.7%), JAK inhibitors (1.7%), intravenous immunoglobulin (IVIG, 1.4%), convalescent plasma (0.9%), remdesivir (0.9%), and ciclesonide (0.6%). No patient received interferon or bevacizumab, and in 13 (3.8%), the treatment used was unknown. The use of azithromycin was reported in 32.3%, clarithromycin in 1.4%, and other unspecified antibiotic in 16.7%.
Regarding complications associated with COVID‐19 infection, 67.4% did not report any complications. However, acute respiratory distress syndrome (ARDS) occurred in 21% of patients, with sepsis in 6.3%, myocarditis or heart failure in 0.9%, concomitant or secondary lung infection in 3.5%, acute kidney injury in 5.5%, and thrombotic events in 2.6%. Regarding the latter, 4% of patients had a personal history of thrombophilia or a state of hypercoagulability; 67.4% hadn’t had such history, and in 24.5%, it was unknown.
In 323 patient records, there was information about the mortality of the disease. A total of 13.3% of the patients died from COVID‐19 or associated complications (Table 2).
We collected a total of 730 questionnaires in both Spanish and Portuguese with information regarding 347 patients from 25 countries in the Latin American region. To the best of our knowledge, it is the largest registry of its kind in the region.
The majority of the patients were female, which coincides with previous reports in the literature. 2 , 4 The average age at presentation was 40.87 years, and phototypes III and IV were the most frequent, consistent with the study population (Latin American countries with a high percentage of mestizo population).
Several groups of researchers have gathered information on cutaneous manifestations, describing and categorizing them with the aim of identifying suspected cases of SARS‐CoV‐2 infection (Table 3). 2 , 3 , 4
Author, region/country | Year | Number of patients | Dermatological manifestations |
---|---|---|---|
Galván‐Casas et al ., 2 Spain | 2020 | 375 | Acral ischemia Pseudo‐chilblains Vesicular Urticarial Rash containing macules and papules |
Servicio de dermatología MQ y V del Hospital Universitario Virgen de las Nieves de Granada, 3 Spain | 2020 | Not specified | Rash (erythematous, petechial, morbilliform) Urticarial Vesicular Acral ischemia Other (livedo reticularis, follicular petechial purpura) |
Freeman et al ., 4 United States of America | 2020 | 716 | Retiform purpura Vesicular Rash containing macules and papules Urticarial Pseudo‐chilblains |
Ocampo‐Candinani et al., Latin America. | 2020 | 347 | Maculopapular rash Urticarial lesions Papulovesicular lesions Vesicular lesions Pseudo‐chilblains Papular lesions Ecchymosis Petechial purpura Pityriasis rosea‐like lesions Pruritus Palmoplantar dysesthesias Acral necrosis Other (transient livedo, palpable purpura, livedo racemosa, and retiform purpura. |
A study in Spain (a country that for some time was the epicenter of the pandemic in Europe) included 375 patients from April 3 to April 16, 2020, with recent skin eruptions without apparent explanation. 2 Five clinical patterns were identified: (1) pseudo‐chilblains (19%): erythema‐edema with some vesicles or acral pustules on the hands and feet, usually asymmetrical; (2) vesicular eruptions (9%): monomorphic vesicles with liquid or hemorrhagic content; (3) urticaria (19%), predominantly in the torso and less frequently in the palms; (4) other (47%): macules and papules with peripheral distribution accompanied by desquamation, also described as pseudovesicles, simulating erythema multiforme; (5) livedo or necrosis (6%), which suggests vascular occlusive disease in the torso or acral ischemia. In addition, the surveyed dermatologists reported an increase in herpes zoster in cases of COVID‐19.
The Spanish dermatological group of the Hospital Universitario Virgen de las Nieves (Virgen de las Nieves University Hospital), 3 described the following patterns: (1) erythematous exanthem/rash, nonspecific, similar to other viral rashes, predominantly in the torso, asymptomatic or with mild pruritus. It appeared at the onset of respiratory symptoms or days later and resolved spontaneously; (2) urticarial rash with erythema and wheals, a nonspecific presentation clinically indistinguishable from acute urticaria, present in 1.4% of patients with COVID‐19; (3) vesicular varioliform eruption (only pattern with vesicles); (4) erythematous lesions similar to acroischemic perniosis (pseudo‐chilblains), initially asymptomatic and can subsequently cause pain and affect acral areas. This pattern was observed more frequently in young oligosymptomatic patients on the dorsolateral aspects and tips of fingers, soles, and heels. After 2 weeks, the lesions became purpuric; (5) other: lesions similar to livedo reticularis on the thighs; follicular petechial purpura on the limbs, torso and, less frequently, the face. The report also described rashes similar to pityriasis rosea, dengue (with low platelet count), infectious erythema, and eruptive pseudoangiomatosis. Some hospitalized patients presented with miliaria crystallina/rubra and folliculitis.
In the United States, a similar study was carried out with patients from 31 countries (the majority from the United States, 89%) and found that among patients with laboratory‐confirmed COVID‐19, the most common morphologies were morbilliform rash (22%), pseudo‐chilblains (18%), urticaria (16%), macular erythema (13%), papulosquamous lesions (9.9%), and retiform purpura (6.4%). 4 Pseudo‐chilblains presentation was more common in patients with moderate disease, while retiform purpura presented exclusively in severely hospitalized patients.
The vast majority of respondents concluded that the dermatological manifestations of their patients were probably related to COVID‐19 infection, and PCR was the most frequently used confirmatory method. In our study, the main dermatological patterns were maculopapular rash, urticarial lesions, papulovesicular rash, vesicular rash, and pseudo‐chilblain lesions, which coincides with previous reports in the literature 2 , 4 and represents a spectrum of manifestations as broad as that reported by Freeman et al. 4 We also report previously undescribed symptoms: pruritus and palmoplantar dysesthesias. Some hypotheses that could explain the pruritus are the exacerbation of preexisting itchy disorders, secondary reactions to personal protective equipment (PPE), psychological stress‐induced itch, and directly related to the dermatoses associated with the COVID‐19 infection. 5 Palmoplantar dysesthesias, without redness or swelling, could be secondary to the already widely recognized occlusive vasculopathy due to COVID‐19 infection or to symptomatic therapy. SARS‐CoV‐2 is not the only virus that can cause burning sensations on hands and feet as several outbreaks of poxvirus‐related burning sensation have been reported in China but accompanied with redness and swelling (erythrodysesthesia). 6 A histopathological study was performed in a minority of patients, probably due to the transient nature of the clinical manifestation, the overall condition and isolation of the hospitalized patients, and because the vast majority of the patients only required outpatient management. Similar to Suchonwanit, 7 we consider that the manifestations of COVID‐19 could be a response to viral antigens or secondary to phenomena such as vasculitis or thrombotic vasculopathy, which are widely recognized systemic consequences of COVID‐19 infection. Regarding this, we found that the majority of our patients (67.4%) did not present any complications; however, ARDS, sepsis, heart failure, concomitant lung infection, acute kidney injury, and thrombotic events were reported as important complications.
The majority of our patients had mild signs and symptoms of the disease, which correlates with the greater frequency of clinical manifestations related to COVID‐19, probably associated with hypersensitivity to virus particles. 7 Most maculopapular rashes occurred during the active phase of the disease, which may correlate to the viremia phase; regarding the prevalence of cutaneous manifestations associated with symptomatic cases of COVID‐19 infection, it is suggested that SARS‐CoV‐2 infection lead to hypercytokinemia and expression of interferon‐inducible genes which have multiple immunopathogenic potentials including overexpression of genes involved in inflammation, which can explain most of the cutaneous signs and symptoms. 8 It is worth noting that no patient received interferon or bevacizumab, the former of which is associated in some case reports with pseudo‐chilblain manifestations. 9 , 10 , 11 The majority of the patients recovered and required mostly supportive treatment. However, age and the presence (or absence) of comorbidities are determinants of the implementation of different therapeutic strategies.
The knowledge and identification of dermatological manifestations in patients infected with the SARS‐CoV‐2 virus can benefit dermatologists and first‐contact physicians, who should become familiar with these symptoms. This registry emphasizes skin manifestations as an important criterion for establishing the diagnosis of COVID‐19 infection in Hispanic patients. This information will be useful for the early identification of suspected cases by health professionals (nondermatologists), which will allow to make recommendations regarding isolation measures for asymptomatic or paucisymptomatic patients, also allowing contact tracing to mitigate the impact of the disease on the health systems at different levels.
We thank all the dermatologist societies of the participating countries, the more than 700 dermatologists involved, all health professionals, and all patients who have become ill from this disease. We also thank Galderma who supported the construction of the digital platform for the questionnaires.
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