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      Psoriasis Over Healed Herpes Zoster: Wolf's Isotopic Response

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          Abstract

          Sir, The term “Wolf's isotopic response” refers to the occurrence of a new unrelated dermatosis at the same location as a previously healed dermatosis.[1] The most common preceding dermatosis is herpes zoster. Many dermatological entities can develop at the site of healed herpes zoster such as granulomatous processes, papulosquamous diseases, lymphomas, pseudolymphomas, primary skin tumors, and metastatic deposits.[2] We hereby describe a patient who developed psoriatic lesions on the site of previous herpes zoster. A 35-year-old female who had suffered from herpes zoster 6 months back consulted for a rash that had been present for the preceding 2 weeks, over the healed lesions of herpes zoster, corresponding to the left thoracic dermatomes T8–T10. To start with, there a few scaly, red, and elevated lesions over the healed areas of herpes zoster, which increased in number and dimensions to attain the present status. Cutaneous examination showed multiple erythematous scaly papules coalescing to form plaques distributed over the left T8–T10 dermatomes [Figure 1]. Besides, there were a few hypopigmented patches in the vicinity of the psoriatic lesions, which represented postinflammatory hypopigmentation marks following herpes zoster. Skin biopsy was done from an erythematous papule, and the histopathology showed hyperkeratosis, parakeratosis, acanthosis, neutrophilic microabscesses, edematous papillary dermis, and dilated blood vessels [Figure 2]. Dermoscopy showed regular arrangement of dotted vessels and white scales [Figure 3]. Based on clinicopathological correlation and dermoscopy, the diagnosis was confirmed as psoriasis. Taking into consideration the preceding history of herpes zoster, our case was a classical example of Wolf's isotopic response wherein psoriasis developed at the sites of healed herpes zoster. Figure 1 Clinical photograph showing erythematous scaly plaques present over the site of healed herpes zoster Figure 2 Histopathology shows hyperkeratosis, parakeratosis, acanthosis, neutrophilic microabscess, suprapapillary thinning, and dilatation of dermal vessels (H and E, ×10) Figure 3 Dermoscopy shows white scales (black arrow) and regular arrangement of dotted vessels (blue circle) (Heine Delta 20 Polarized) It was the first time in 1955 when Wyburn-Mason described the occurrence of a new unrelated disease at the site of a previously healed disease.[3] This was coined as “isoloci response” by Wolf in 1985.[4] Later on, it was renamed as “isotopic response” followed by “Wolf's isotopic response.”[1 5] The dermatoses which are known to present in the site of previously healed disease include granulomatous reactions, malignant tumors, leukemic infiltrates, dermatoses secondary to immunologic dysfunction, infections, comedogenic reactions, and other miscellaneous conditions.[6] The etiopathogenesis behind this response remains inconclusive. Various hypotheses have been put forward. However, the neural hypothesis is the most accepted one. During herpes zoster, varicella zoster virus causes destruction of the A-delta and C nerve fibers. Besides, neurohumoral factors stimulate the development of the second dermatosis by releasing substance P, bradykinin, serotonin, vasoactive intestinal peptide, calcitonin gene-related peptide, and α-melanocyte-stimulating hormone. These neuropeptides initiate the immunological cascade of the pathogenesis of the second disease. In addition to this, neurohumoral factors lead to unregulated activation of the immune system which contributes to the isotopic response. Allegue et al. proposed the role of tumor necrosis factor alpha (TNF-alpha) in the pathogenesis of this isotopic response. TNF-alpha is known to possess antiviral activity, and the levels are elevated in herpes zoster. Besides, TNF-alpha is also elevated in psoriatic skin lesions. Therefore, it can be hypothesized that increased levels of TNF-alpha during the course of herpes zoster could serve as a triggering factor for the development of psoriasis over the healed sites.[6] Numerous dermatoses have been reported to occur as a part of Wolf's isotopic response. However, psoriasis is a rarely reported condition. Allegue et al. documented a case of psoriasis developing over T6 and T7 dermatomes in a known case of healed herpes zoster.[7] Our case adds to the list of documented examples of Wolf's isotopic response over the sites of healed herpes zoster. The second dermatosis being psoriasis adds to the uniqueness of the present report. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.

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          Isotopic response.

          The occurrence of a new skin disorder exactly at the site of another one, already healed and unrelated, was first described in 1955. In 1985, Wolf et al. recognized that we are dealing with a dermatologic phenomenon and established a precise definition for this phenomenon. Fifty-eight cases corresponding to the definition of this phenomenon have been reported until now. The new phenomenon, for which the term "isotopic response" has been suggested, has been defined. Cases corresponding to the definition have been analyzed with special emphasis on the diseases involved, the time intervals, and the locations of the diseases. Eight new cases are described. A total of 58 cases of isotopic response have been described. The first disease in most of the patients was herpes zoster; in three cases it was herpes simplex, in two varicella, and in one, thrombophlebitis. The second disease, which appeared exactly at the site of the first, already healed disease, was in most reported cases a carcinoma (26 cases, in particular 15 cases of breast carcinoma, 5 basal cell carcinomas (BCC), 4 squamous cell carcinomas (SCC), 2 basosquamous carcinomas), or granuloma annulare (16 cases). Additional diseases were Kaposi's sarcoma (2 cases), pseudolymphoma (2 cases), sarcoid (2 cases), tinea (2 cases), tuberculoid and vasculitis granuloma (1 case), angiosarcoma, metastasis, Bowen's disease, lymphoma, leukemia cutis, and acne (1 case each). The diseases did not show any predilection for a particular location. The interval between the first and second disease was extremely variable (ranging from days to years) and showed no particular features. In the eight additional cases described in the present report, the first disease was herpes simplex (6 cases) or herpes zoster (2 cases). The second disease was viral warts (3 cases) or squamous cell carcinoma (2 cases). Additional diseases were furunculosis, contact dermatitis, and molluscum contagiosum (1 case each). The new term, "isotopic response," describes the occurrence of a new skin disorder at the site of another, unrelated, and already healed skin disease. It is suggested that the term "isotopic response" be included in the lexicon (glossary) of dermatology. Introducing the new term and classifying all the cases under a single key word, will make it possible to locate and collect them easily and to search for the mechanism underlying this phenomenon.
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            Isotopic response after herpesvirus infection: an update.

            The term postherpetic isotopic response describes the occurrence of a new, unrelated disease that appears at the same location as a previously healed herpetic infection. When dealing with the pathogenetic mechanism involved in the isotopic response, several possibilities should be considered: a viral origin, an immunologic origin, a vascular origin, and a neural origin. The aim of this article is to review and discuss the different pathogenetic mechanisms with particular attention to new information related to the possible neural origin of this abnormal response of the skin.
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              Wolf's Isotopic Response: Report of a Case and Review of Literature

              “Wolf's isotopic response” refers to the occurrence of a new dermatosis at the site of previously healed dermatosis. A number of factors including viral, neural, vascular, and immunologic factors have been implicated in the causation of this peculiar response but none has been proven conclusively. Here, we report a case where lichen planus developed at the site of dermatofibrosarcoma protruberans that had been previously treated with surgery and radiotherapy. We also put forth a hypothesis on the genesis of isotopic response considering the above mentioned factors.
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                Author and article information

                Journal
                Indian J Dermatol
                Indian J Dermatol
                IJD
                Indian Journal of Dermatology
                Medknow Publications & Media Pvt Ltd (India )
                0019-5154
                1998-3611
                Sep-Oct 2017
                : 62
                : 5
                : 542-544
                Affiliations
                [1] From the Department of Dermatology, Command Hospital, Kolkata, West Bengal, India. E-mail: shekharadvait@ 123456gmail.com
                [1 ] Department of Dermatology, KPC Medical College and Hospital, Kolkata, West Bengal, India
                [2 ] Department of Pathology, Command Hospital, Kolkata, West Bengal, India
                Article
                IJD-62-542
                10.4103/ijd.IJD_661_16
                5618852
                fab132dd-221c-4c46-87e8-bafe8b2c79d3
                Copyright: © 2017 Indian Journal of Dermatology

                This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

                History
                : November 2016
                : August 2017
                Categories
                Correspondences

                Dermatology
                Dermatology

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