key: cord-0961798-xxamhzgd authors: Lotfi, Zahra; Haghighi, Anousheh; Akbarzadehpasha, Amirhossein; Mozafarpoor, Samaneh; Goodarzi, Azadeh title: Pansclerotic Morphea Following COVID-19: A Case Report and Review of Literature on Rheumatologic and Non-rheumatologic Dermatologic Immune-Mediated Disorders Induced by SARS-CoV-2 date: 2021-10-20 journal: Front Med (Lausanne) DOI: 10.3389/fmed.2021.728411 sha: d11c879da4066fe7025489e50bd27d0b9bde9ef9 doc_id: 961798 cord_uid: xxamhzgd While mucocutaneous manifestations of COVID-19 have been frequently reported and added to our knowledge every day during the pandemic, another issue is the COVID-related diseases that can present as intensified lesions of underlying diseases, a new disease, or changes in the behavior of an old lesion. Given that immune system overreaction and cytokine storm are among the most prominent events in COVID-19, the incidence of autoimmune diseases is expected to increase after COVID-19, as confirmed in several reports. To increase the body of knowledge about short- and long-term outcomes of COVID-19 for specialists, it is essential that similar cases be reported and collected for years to come. The present study investigated a case of pansclerotic morphea that rapidly progressed a few weeks after infection with COVID-19 in a 57-year-old woman with no history of any autoimmune skin or rheumatic diseases. She was prescribed outpatient COVID-19 treatment of azithromycin, vitamins D and C, and then quarantined for 2 weeks. The manifestations of the disease were exacerbated at each follow-up and sampling visit at short intervals. This kind of pansclerotic morphea is reported for the first time. The outbreak of the new SARS-CoV-2 has rapidly spread and infected many people throughout the world since early 2020 (1) . Meanwhile, the complications brought by the virus have concerned many people. Given that viruses trigger immune responses, it is predictable that viral diseases cause autoimmune diseases through the viral attack itself or the immune dysregulation due to inflammatory responses. The skin is one of the most important organs that manifest the symptoms and complications of COVID-19 through various types of lesions including exanthematous rashes, urticarial rashes, and mucosal lesions. Since many chronic skin diseases are mediated by immune responses, specialists are in dire need of knowledge about COVIDinduced skin diseases. To date, a number of such lesions have been investigated and reported in published articles (2, 3) . The effect of COVID-19 on autoimmune skin diseases can appear as exacerbation of a pre-existing disease (4) , changes in manifestations of the disease (5), or causing the disease for the first time. It is worth noting that some of these diseases are exacerbated because patients discontinue immunomodulatory medications, which have been discussed in detail in published guidelines (6) . This is the first case report of pansclerotic morphea (PSM) following COVID-19. In this study, a new case of pansclerotic morphea following COVID-19 infection in a 57year-old previously healthy woman was studied. After her first symptoms of malaise and stiffness of skin and myalgia, an internal medicine referred her to the rheumatologist. Then a dermatology consult was demanded after some lab tests showing high amounts of ANA and Anti-ds DNA and CRPa. Manifestations of generalized skin stiffness were noted, especially on shins, arms, and abdomen, wherein some areas had the peau d'orange feature. Afterward, a deep biopsy of the skin for further investigations was performed which resulted in sclerodermoid changes. According to clinical examination, the final diagnosis was post-COVID PSM. A 57-year-old woman with no underlying diseases attended our internal disease clinic on October 15, 2020, presenting with respiratory symptoms, general weakness, and myalgia. Once her PCR test for SARS-CoV-2 was reported positive, she was prescribed outpatient COVID-19 treatment of azithromycin, vitamins D and C, and quarantined for 2 weeks. A retest of that patient on October 28, 2020, was negative, so she resumed her daily functions. During recovery, symptoms of weakness and myalgia persisted, to which arthralgia and arthritis of the ankles and knees were added. Furthermore, difficulty in performing knee flexion impaired the daily functions of the patient. The examinations carried out by the internist ruled out deep vein thrombosis (DVT), hemostasis problems, and heart failure. The lab tests showed high platelet count and ESR, so the physician ordered a complete rheumatology panel. The test results revealed higher than normal ranges for Antinuclear Antibody (ANA), anti-double stranded (anti-ds) DNA, Angiotensin-Converting Enzyme (ACE), and C-reactive protein (CRP). At this stage, the patient was referred to a rheumatologist for further investigations regarding suspected collagen-vascular diseases. The rheumatologist ordered the tests again, which revealed ACE to be higher than the normal range while ANA and antids DNA were negative. Physical examination revealed taut skin and subcutaneous tissue of the left upper limb, in addition to arthritis and arthralgia, so the patient was referred to the dermatology department for a scleroderma work-up. Changes in favor of scleroderma morphea were observed in the first visit of the patient to the dermatology clinic. Physical examination revealed the skin had turned shiny and tight (Figure 1 ). When touched, the skin felt rather sclerotic and lost the ability to fold compared with normal skin. Severe sclerosis was observed in both pretibial regions. In addition to changes in the arm and lower abdomen in favor of morphea, clinically deep morphea could not be differentiated from eosinophilic fasciitis. Therefore, a deep biopsy was performed on the left pre-tibial and left arm regions which showed changes in favor of sclerodermoid changes and no sign of eosinophilic fasciitis (Figure 2 ). Reexamination 2 weeks later revealed the exacerbation of previous lesions, newly formed lesions that rapidly spread to the proximal lower limbs and distal upper limbs, and difficult and painful movement of the limb. The pathology report corresponded to scleroderma/morphea in both regions. Treatment initiated with corticosteroids and the patient underwent further examinations while the case report was being written. The timeline of events can be seen in Figure 3 . Given the high levels of CRP and ACE in the lab tests, a CT scan on the lungs was carried out. The CT scan showed a mass in the upper lobe of the right lung, so the patient underwent a needle biopsy, which led to the diagnosis of lung adenocarcinoma. Next, a PET-scan of the lung was performed to assess staging of the adenocarcinoma, and the patient underwent lobectomy of the right lung. Given the patient's underlying conditions, the systemic treatment for morphea was postponed and the patient received only topical medications until the results of the lung cancer assessment were ready. At this stage, the lesions of the patients had stabilized and tissue pain and tenderness reduced. Afterward, lung lobectomy surgery was performed, and the tumor was excised completely. During the follow ups, there were no signs of tumor recurrence. Considering her condition, we preferred to treat her skin condition with topical therapy with corticosteroids and emollients. Then, the patient declared an improvement in pain and stiffness of the skin. Given the onset of these lesions and their rapid spread immediately after infection with COVID-19, the imbalance of immunomodulatory factors and the activation of the autoimmune response to the virus were considered to have triggered this rapid spread. Lung cancer was accidentally found during the follow-up. Although morphea has been reported as a paraneoplastic syndrome in various types of cancer such as lung small cell carcinoma or breast carcinoma (7-9), it has not been reported as a paraneoplastic phenomenon after adenocarcinoma of the lung. Therefore, its occurrence in this patient can be more attributed to COVID-19 complications. This is the first report of this type of PSM after COVID-19 infection. Morphea, also known as localized scleroderma, is a chronic autoimmune disease identified by skin inflammation and Frontiers in Medicine | www.frontiersin.org sclerosis. Scleroderma and morphea are diagnosed with skin sclerosis and have common pathological manifestations. Both diseases present with dermal and subcutaneous sclerosis and no fibroblast proliferation. However, morphea is different from scleroderma in demographic and clinical terms. Unlike scleroderma, involvement of the internal organs is uncommon and the mortality rate is lower in morphea. Different types of morphea are shown in Table 1 (10) . The generalized morphea is identified by more than four plaques of at least 3 cm that involve two or more anatomical regions. This type of morphea is differentiated from scleroderma by the absence of Raynaud's, sclerodactyly, no facial involvement, no nail fold involvement in capillaroscopy, no visceral involvement, and no specific autoantibodies. Although systemic sclerosis has been reported as a paraneoplastic phenomenon, the association of morphea with cancer has not been demonstrated (11) . Pansclerotic morphea is a type of severe and progressive generalized morphea that deeply spreads into the subcutaneous tissue and invades the muscles, tendons, and bones. The lesions normally appear on the extensor side of the four limbs and trunk, and gradually affect the entire body surface, including the head and neck, causing joint stiffness, deformity, ulceration, and calcification. Squamous cell carcinoma has been reported on the skin lesions of this kind of morphea (12) . Disabling PSM of childhood (DPMC) is a rare subtype of juvenile localized scleroderma (JLS) characterized by pansclerosis mainly affecting children under the age of 14. This aggressive disease has a poor prognosis due to the rapid progression of deep musculoskeletal atrophy resulting in cutaneous ulceration and severe joint contractures (13) . Given the stiffness and swelling of the knee in the patient, the above-discussed case was considered to be of PSM type. There has been much concern about the effect of COVID-19 on the incidence or exacerbation of autoimmune diseases since the outbreak of SARS-CoV-2. Numerous papers have been published about the effects of COVID-19 on the exacerbation of autoimmune diseases. The experience of COVID-19 in people with underlying skin diseases, such as psoriasis, lupus, and rheumatoid arthritis, was documented over time and led to recommendations for modifying the administration of immunomodulatory medications during the pandemic. However, the new cases of these diseases following infection with SARS-CoV-2 when the initial symptoms of COVID-19 abate. Given the high burden of collagenvascular and chronic skin diseases on the life of the patient, we decided to gather and review articles investigating the incidence of new skin diseases reported after COVID-19 to draw the attention of specialists to this important issue (Tables 2, 3) . COVID-induced collagen-vascular diseases are presented in Table 2 , and other COVID-induced skin diseases in Table 3 . It should be noted that COVID-19 vaccination might have some similar effects on immune system responses and cause autoimmune diseases, as there have been some reports to date (14, 15) . Therefore, similar reviews of literature and more investigations on that topic are recommended. It is recommended that reports of new cases of skin diseases be gathered in review articles to help specialists in this field properly diagnose, treat, and manage such diseases. During the pandemic, the authors especially focused on various skin manifestations of COVID-19 in their research on the subject (16) (17) (18) (19) (20) (21) (22) (23) (24) (25) (26) (27) (28) (29) . Our study had a limitation. We did not long-term follow-up. Because of the pandemic, the authors decided to release the information to be available to researchers as soon as possible. Thus, the diagnosis of lung cancer in between may have affected the results. However, the importance of our study is that it reported a unique and new manifestation, which is the first case of a particular type of autoimmune disease following COVID-19. The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s. Written informed consent was obtained from the patient for participation in the study and the rights of the subject were protected. To observe ethical principles, the names of the patients were not mentioned in the paper. Written informed consent was obtained from the patient for publication of this case report and any accompanying images. All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication. 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