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      Finger pad tophi in gout: a rare presentation*

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          Abstract

          To editor, Gout is a common rheumatological disease caused by a disturbance in uric acid metabolism. Tophi develop during most advanced clinical stage of gout, and usually present as firm pink nodules or fusiform swelling, mainly at periarticular sites. However, unusual skin manifestations caused by intradermal and subcutaneous deposition of tophaceous material at locations other than periarticular regions have been reported. 1-3 We presented a case of a 65-year-old with 2-years history of multiple, whitish, milia-like, firm papules over the finger pads (Figure 1). The patient had intense alcohol use and up to 3 kg/day meat consumption for 20 years. Laboratory tests showed raised levels of uric acid (10.8 mg/dl; normal range 3.4-7 mg/dl), creatinine and cholesterol. Punch biopsy was performed from a typical papule. On histopathological examination, numerous, parallel-lined, needle-like, brown monosodium urate (MSU) crystals and a deposit of pink amorphous material consisting with MSU were seen in the dermis. These crystals showed negatively birefringent under polarized light (Figure 2). Based on the clinical, histopathological and laboratory findings a diagnosis of intradermal tophaceous gout was made. He was referred to rheumatology for management of gout. Figure 1 (A-B) Multiple, whitish, milia-like, firm papules over the finger pads Figure 2 Multiple, needle-like monosodi - um urate crystals were visible under polarized light The natural history of gout involves four clinical stages; asymptomatic hyperuricemia, acute gouty arthritis, intercritical gout and chronic tophaceous gout. Some atypical forms of tophaceous gout have been described, including bullous, fungating, ulcerative gout, gouty panniculitis and miliarial gout. 1-5 Intradermal tophi are rare skin manifestations of chronic gout that are characterized by multiple, tiny, superficial, pustule or milia-like, whitish lesions. 3-5 Rarely they appear at extra-articular sites such as forearms, arms, finger pad, legs, buttock, thigh, penis, vocal cords, epiglottis, tongue and abdominal wall. 1-3 In our patient, the intradermal gout lesions were restricted to the finger pads. Risk factors predisposing to the development of intradermal gout include renal insufficiency, hypertension, long-term use of furocemid and corticosteroids, long-term duration of disease, obesity, and lack of consistent use of urate-lowering therapy. 1,4 The present case had some of this risk factors. The differential diagnosis of intradermal tophi includes xanthoma and calcinosis cutis, which can be easily diagnosed by examining fluid in polarized light or performing biopsy. 1,2,5 Allopurinol and colchicine have been reported to improve intradermal gout, and our patient was referred to a rheumatologist for management but was lost to follow-up. In conclusion, the incidence of gout is increasing, possibly due to an aging population and eating habits. This case illustrates the importance of considering a rare cutaneous manifestation of gout.

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          Most cited references10

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          Intradermal urate tophi.

          A Fam, D Assaad (1997)
          To analyze the clinical features and identify risk factors associated with the development of intradermal urate tophi.
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            Intradermal tophi in gout: a case-control study.

            To describe the characteristics of intradermal tophi in patients with gout and search for factors associated with their development.
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              Unilateral milia-type intradermal tophi associated with underlying urate subcutaneous deposition: an uncommon cutaneous presentation of gout.

              Tophi develop during the most advanced clinical stage of gout, and are usually located on or around the joints. However, unusual skin features caused by intradermal and/or subcutaneous deposition of tophaceous material at locations other than articular regions have been reported. We present the case of a patient with a condition that has been recently termed 'miliarial gout'. which is only the second such case, to our knowledge. A 51-year-old woman, who had a chronic joint disease that had been diagnosed and treated as psoriatic arthritis, presented with multiple asymptomatic, yellowish-white, firm papules (1-3 mm in size) on erythematous areas on the outside of her left leg. On histological examination of a skin biopsy, uric acid crystals were seen in the dermis and subcutis. The patient also had a raised level of serum urate, consistent with a diagnosis of gout. Treatment with allopurinol led to rapid improvement. Intake of corticosteroids and diuretics was a possible triggering factor for the development of cutaneous tophi in this patient.
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                Author and article information

                Journal
                An Bras Dermatol
                An Bras Dermatol
                abd
                Anais Brasileiros de Dermatologia
                Sociedade Brasileira de Dermatologia
                0365-0596
                1806-4841
                Nov-Dec 2016
                Nov-Dec 2016
                : 91
                : 6
                : 855-856
                Affiliations
                [1 ] Şişli Hamidiye Etfal Training and Research Hospital, Dermatology Department - Istanbul, Turkey
                [2 ] Şişli Hamidiye Etfal Training and Research Hospital, Pathology Department – Istanbul, Turkey
                Author notes
                Mailing address: Aslı Aksu Çerman, Şişli Hamidiye Etfal Training and Research Hospital, Dermatology Department, Halaskargazi Cad, Etfal S, 34360 Şişli/Istanbul/Turkey. Email: aksuasli@ 123456hotmail.com
                Article
                10.1590/abd1806-4841.20164466
                5193211
                b65c717a-65e3-43da-8767-c6c2fe367de9

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 16 February 2015
                : 07 April 2015
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