Literature DB >> 34309940

Cutaneous manifestations of patients hospitalized with coronavirus disease 2019 (COVID-19).

P Ramezani Darmian1, Z Memarzadeh1, R Aryan1, Y Nahidi1, Z Mehri1, A Taghipour2, N Samimi3, M Amini4, P Layegh1.   

Abstract

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Year:  2021        PMID: 34309940      PMCID: PMC8447134          DOI: 10.1111/jdv.17557

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   9.228


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Conflicts of interest

The authors declare no conflict of interest.

Funding sources

This research was supported by the Vice Chancellor for Research of Mashhad University of Medical Sciences under grant number 990169.

Ethical approval

All procedures involving human participants were in accordance with the ethical standards of the national research committee and the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

All patients or their legal guardians signed informed consent regarding publishing their data and photographs. Dear Editor In December 2019, a new member of the coronavirus family emerged in Wuhan city in Hubei Province of China, and rapidly spread all over the world causing a pandemic. , A recent Cochrane review categorized different presentations of coronavirus disease 2019 (COVID‐19) into four groups: respiratory, systemic, cardiovascular and gastrointestinal. However, some bizarre manifestations like olfactory problems, thrombotic events and even mental problems may exist with this infection. One of these rare presentations is skin involvement that can even be the first presentation of the disease. Dermatologic signs and symptoms of COVID‐19 are diverse and still need investigation to be completed. We conducted a study between September and October 2020 on 387 COVID‐19 hospitalized patients in Imam Reza Hospital of Mashhad, Iran. All COVID‐19 cases were confirmed according to the diagnosis of pulmonologists and infectious disease specialists based on polymerase chain reaction test or high‐resolution computed tomography of the chest. All patients were visited by an academic dermatologist and a volunteer resident of dermatology at the patients' hospital beds. Initially, the preliminary data including age, gender, demographic information, past medical history, drug history, clinical and laboratory findings of each patient were extracted from their medical files. Then, cooperative patients were asked about the history of any dermatologic lesion from a few weeks before clinical signs and symptoms of COVID‐19 appear up to this point. Those with a positive history of these lesions were examined to define the distribution of the lesion. Furthermore, a full history regarding their dermatologic symptoms, any past medical history or family history of a skin problem was taken. For ill patients, physical examination of the skin was performed by a dermatologist. Photographs were also taken of all the patients' lesions. Additionally, we followed up each patient by telephone calls 2 weeks after each visit in order to detect further skin involvements. All the lesions' photographs were reviewed by three academic dermatologists and the final diagnosis was made based on their consensus. Skin biopsies were conducted in some cases that seemed necessary. The study protocol was approved by the Institutional Ethics Board of Mashhad University of Medical Sciences (IR.MUMS.REC.1399.175). Written informed consent was signed by all patients or their legal guardians for those with very severe or unconscious conditions. P‐value < 0.05 was considered statistically significant. All analyses were performed using SPSS software version 11.5 (SPSS Inc., Chicago, IL, USA). A total of 387 patients including 205 males and 182 females were enrolled in this study. The details of demographic and baseline data of the patients are presented in Table 1.
Table 1

Demographic and baseline data of the patients

FeatureFrequencyPercent
GenderMale20553.0
Female18247.0
Admitted wardICU5714.8
General32985.2
COVID‐19 Diagnosis methodPolymerase chain reaction12331.8
Clinical signs and high‐resolution computed tomography26468.2
Hospitalization duration≤1 week14036.6
>1 week24263.4
OutcomeRecovery31882.0
Death6918.0
Past medical historyHypertension19049.1
Cardiac disease13534.9
Cerebrovascular accident82.1
Diabetes8421.7
Renal disease4411.4
Dyslipidaemia21455.3
Clinical signsRespiratory29476
Constitutional16743.2
Gastrointestinal307.7
Neurologic359.0
Other20.5
TreatmentsImmunosuppressive10326.6
Anti‐epileptic338.5
Antiviral (Kaletra)11529.9
Hydroxychloroquine33687.5
Azithromycin35391.9
Ceftriaxone36695.3
Heparin36494.8
Dexamethasone5414.1
Anti‐inflammatory6015.6
AddictionYes9023.3
No29776.7
Demographic and baseline data of the patients The most prevalent accompanying disease was dyslipidaemia (214 cases; 55.3%) followed by hypertension (190 cases; 49.1%). Respiratory symptoms were present in 294 patients (76%); 167 patients (43%) experienced constitutional signs and symptoms; 29 (7.5%) had cutaneous involvement in the presence of COVID‐19 infection; 15 cases (3.9%) had dermatological symptoms before and 14 patients (3.6%) during hospitalization. Moreover, four patients (1.0%) developed skin symptoms before, 12 (3.1%) during and 13 (3.4%) after presentation of other clinical symptoms of COVID‐19 infection. The most common type of skin lesions was papule/plaque (nine cases; 2.3%) and the diagnoses of our cases included livedo reticularis/racemosa, pityrasis rosea like, herpes labialis, herpes zoster, maculopapular viral exanthema, urticarial viral rash, acral peeling, contact dermatitis and drug reaction in which the most common were livedo reticularis/racemosa (four cases; 1.0%) and acral peeling (four cases; 1.0%). There was no significant difference regarding age, gender, underlying diseases, CRP and lymphocyte levels, ICU admission and outcome of the disease in patients with different cutaneous diagnoses. (Table 2). Further studies are needed to complete these results.
Table 2

Final diagnosis of skin lesions in different genders, age groups, hospitalization statuses and disease outcomes

FeatureGenderHospitalization statusAgeDisease outcome
MaleFemale P ICUNon‐ICU P <3030–60>60 P RecoveryDeath P
Final diagnosis: frequency (%)Pityrasis rosea like1 (6.3)0 (0)0.40 (0)1 (4.8)0.40 (0)1 (6.3)0 (0)0.51 (5)0 (0)0.14
Herpes labialis1 (6.3)1 (7.7)0 (0)2 (9.5)0 (0)1 (6.3)1 (8.3)2 (10)0 (0)
Herpes zoster0 (0)2 (15.4)1 (14.3)1 (4.8)0 (0)2 (12.5)0 (0)1 (5)0 (0)
Maculopapular viral exanthema2 (12.5)1 (7.7)1 (14.3)1 (4.8)0 (0)2 (12.5)0 (0)2 (10)0 (0)
Drug reaction1 (6.3)2 (15.4)0 (0)3 (14.3)0 (0)0 (0)3 (25.0)2 (10)0 (0)
Livedo reticularis/ rasemoca1 (6.3)3 (23.1)2 (28.6)2 (9.5)1 (100)2 (12.5)2 (16.7)1 (5)3 (50)
Acral peeling4 (25.0)0 (0)0 (0)4 (19.0)0 (0)3 (18.8)1 (8.3)3 (15)1 (16.7)
Contact dermatits1 (6.3)2 (15.4)2 (28.6)1 (4.8)0 (0)1 (6.3)2 (16.7)1 (5)1 (16.7)
Urticarial viral rash2 (12.5)0 (0)0 (0)2 (9.5)0 (0)1 (6.3)1 (8.3)2 (10)2 (33.3)
Other3 (18.8)2 (15.4)1 (14.3)5 (19.0)0 (0)3 (18.8)2 (16.7)5 (25)5 (83.3)
Final diagnosis of skin lesions in different genders, age groups, hospitalization statuses and disease outcomes
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