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      Rapidly Progressing Generalized Morphea with High Lyme Disease Titer

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          Abstract

          Sir, A 51-year-old male presented with erythematous to brownish ill-defined indurated enlarging plaques on the right leg, left flank, and left anterior chest over 10 days with hardness. All of the lesions were exceeding 5 cm in diameter [Figures 1 and 2]. He did not give tick bite history and never had traveled to the endemic areas of Lyme borreliosis. Biopsy from the right leg showed lymphoplasmacytic infiltrate and fibrosis in the dermis and subcutis [Figures 3 and 4]. Complete blood count, chemistry, HIV testing were normal, and antinuclear antibody, anti-Ro/La, anti-RNP, anti Scl70, anti-centromere antibody were all negative. Lyme disease immunoglobulin G titer was 1:512 and IgM titer was <1:16 in immunofluorescence assay (IFA), but negative in Western blot test. Warthin Starry stain was negative. DNA was not detected in polymerase chain reaction. Figure 1 Erythematous to brown colored, irregularly circumscribed indurated plaques are found from upper thigh to calf Figure 2 Slightly whitish to erythematous irregular shaped indurated patch on chest, around nipple Figure 3 Histopathology of specimen from right calf shows perivascular and interstitial infiltrates of lymphocytes and plasma cells in dermis (H and E, ×40) Figure 4 Patchy fibrosis in the subcutaneous layer, and lymphoplasmacytic infiltrates are found. Trabeculae are thickened in subcutaneous layer (H and E, ×100) Transthoracic echocardiography, electrocardiography, esophagogastroduodenoscopy, colonofibroscopy, chest and abdominopelvic computed tomography, and pulmonary function test were done and all were normal. Oral doxycycline (200 mg/day) for 3 weeks was started due to the possibility of Lyme borreliosis but without response. After systemic corticosteroid administration, the progression was slowed. After discontinuing the medication for 3 months, new skin lesions were found on the left buttock and thigh. Corticosteroid was started again, and the progression was stopped. There was no progression after cessation of medication until reporting. Follow-up IFA and western blot determinations were performed 6 months after the onset of symptom, but the titer did not decrease, and western blot was still negative. Lyme disease, also known as Lyme borreliosis, is a multi-organ infection caused by spirochetes of the Borrelia burgdorferi sensu lato group which are transmitted by ticks of the species Ixodes.[1] Common skin manifestations include erythema migrans, lymphocytoma, and acrodermatitis chronica atrophicans.[1] Recently, there have been some reports linking morphea or lichen sclerosus to B. burgdorferi infection.[1] The presence of antibodies to B. burgdorferi in 50% of patients with morphea was found with enzyme-linked immunosorbent assay (ELISA),[1] but contradictory data have been proposed.[2] Most reports of the association between positive antibody test to B. burgdorferi and morphea come from Europe, and have been rarely found in the USA.[3] Differences between Borrelia strains and prevalence in the USA and in Europe have been raised to explain these conflicting results.[3] B. garinii, B. afzelii, and B. burgdorferi sensu stricto are present in Europe, only B. burgdorferi sensu stricto is identified in the USA. It has been suggested that only certain types of infection of B. burgdorferi may lead to morphea. B. burgdorferi sensu stricto, has never been found in late dermatologic manifestations of Lyme borreliosis, this may explain the reason of conflicting data from different regions.[3] The overall false-positive rate of Lyme borreliosis testing is approximately 5%.[4] When patients have other viral or spirochetal infections or autoimmune diseases, false-positive findings with ELISA or IFA may occur.[4] There has been only one case of morphea with false positivity to Lyme titer since 1993.[5] We experienced this interesting case of rapidly progressing generalized morphea with high antibody titer to B. burgdorferi. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.

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          Most cited references5

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          Cross-reactivity of nonspecific treponemal antibody in serologic tests for Lyme disease.

          Serum samples obtained from 59 persons who had acute necrotizing ulcerative gingivitis, periodontitis, syphilis, or Lyme disease were tested against Treponema phagedenis biotype Reiter, Treponema denticola, Treponema vincentii, and Treponema scoliodontum by indirect fluorescent-antibody staining methods. Although there were positive reactions for sera representing each of these study groups and for 20 (13%) of 156 samples collected from the general population (premarital screening for syphilis), titration endpoints were relatively low (less than or equal to 1:256). Serum samples from 18 persons who had gingivitis or periodontitis but no history of Lyme borreliosis were tested by enzyme-linked immunosorbent assay for antibodies to Borrelia burgdorferi. Of these, five (28%) had immunoglobulin M antibody and four (22%) contained immunoglobulin G antibodies to this spirochete. Adsorption with either sorbent commercially prepared from T. phagedenis biotype Reiter or with washed, whole cells of T. phagedenis biotype Reiter reduced cross-reactivity in the enzyme-linked immunosorbent assay for Lyme borreliosis.
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            Is morphoea caused by Borrelia burgdorferi? A review.

            The aetiology of morphoea and lichen sclerosus et atrophicus is still unknown. Since the detection of Borrelia burgdorferi (B. burgdorferi) as the causative agent of Lyme disease, there has been debate about a possible association between B. burgdorferi and morphoea. Initial serological and cultural studies showed controversial results. The introduction of polymerase chain reaction (PCR) initially suggested an association between B. burgdorferi and morphoea. We reviewed the literature on B. burgdorferi (specific serology, immunohistology, culture, lymphocyte stimulation and DNA detection by PCR) since 1983, using Medline and Current Contents. Histological and immunohistological detection of B. burgdorferi was reported in 0-40% (20 of 82) of the cases with morphoea and in 46-50% (17 of 36) of the cases with lichen sclerosus et atrophicus. Cultivation of spirochetes from lesional skin succeeded in five patients (five of 68) with morphoea, but failed in patients with lichen sclerosus et atrophicus. In Europe and Asia, serological detection of antibodies against B. burgdorferi was described in 0-60% (138 of 609) of patients with morphoea and in 19% (six of 32) in the U.S.A. For lichen sclerosus et atrophicus 0-25% of the published cases (three of 23) in Europe and Asia were seropositive. DNA from B. burgdorferi was detected by PCR in 0-100% (17 of 82) of the tissues of patients with morphoea in Europe and Asia, but not a single case among 98 patients was reported to be positive from the U. S.A. In Europe and Asia, borrelial DNA was detected in 0-100% (nine of 28) of the cases with lichen sclerosus et atrophicus, whereas in the U.S.A. none of 48 patients was positive. There are two possible explanations for these contradictory findings: the most likely is that B. burgdorferi is not a causative agent for morphoea. Another possible explanation could be that a subset of morphoea is caused by a special subspecies of B. burgdorferi that is present in Europe and Asia but does not occur in the U.S.A.
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              Detection of Borrelia burgdorferi DNA (B garinii or B afzelii) in morphea and lichen sclerosus et atrophicus tissues of German and Japanese but not of US patients.

              To elucidate the geographic and genospecific association of Borrelia with morphea and lichen sclerosus et atrophicus (LSA).
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                Author and article information

                Journal
                Indian J Dermatol
                Indian J Dermatol
                IJD
                Indian Journal of Dermatology
                Wolters Kluwer - Medknow (India )
                0019-5154
                1998-3611
                Sep-Oct 2020
                : 65
                : 5
                : 432-434
                Affiliations
                [1] From the Human Dermatologic Clinic, Dankook University, Cheonan, Korea
                [1 ] Department of Dermatology, College of Medicine, Dankook University, Cheonan, Korea. E-mail: ivymyung@ 123456hanmail.net
                Article
                IJD-65-432
                10.4103/ijd.IJD_279_18
                7640786
                219a1b82-d370-4510-be01-9182112194c5
                Copyright: © 2020 Indian Journal of Dermatology

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : June 2018
                : November 2018
                Categories
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                Dermatology
                Dermatology

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