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      Acute arthritis, skin rash and Lofgren’s syndrome

      case-report

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          Abstract

          Sarcoidosis is an autoimmune multisystem granulomatous disorder of unknown aetiology, which mainly affects the adults in the age group of 20–39 years. The disease can affect any organ in the body but mainly presents as bilateral hilar lymphadenopathy, pulmonary infiltrates, cutaneous lesions, ocular manifestations and arthropathy. Lofgren’s syndrome is an uncommon initial presentation of sarcoidosis which is recognised by the classical triad of acute arthritis, erythema nodosum and bilateral hilar lymphadenopathy. We describe a newly diagnosed case of sarcoidosis who presented as Lofgren’s syndrome. Acute sarcoid arthritis should be kept as one of the differential diagnoses for patients presenting with acute arthritis and skin lesions; and chest X-ray should be considered to rule out bilateral hilar lymphadenopathy in these patients. Early suspicion and identification of classical clinical features are essential to establish early diagnosis.

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          Sarcoidosis.

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            Sarcoidosis: Causes, Diagnosis, Clinical Features, and Treatments

            Sarcoidosis is a multisystem granulomatous disease with nonspecific clinical manifestations that commonly affects the pulmonary system and other organs including the eyes, skin, liver, spleen, and lymph nodes. Sarcoidosis usually presents with persistent dry cough, eye and skin manifestations, weight loss, fatigue, night sweats, and erythema nodosum. Sarcoidosis is not influenced by sex or age, although it is more common in adults (< 50 years) of African-American or Scandinavians decent. Diagnosis can be difficult because of nonspecific symptoms and can only be verified following histopathological examination. Various factors, including infection, genetic predisposition, and environmental factors, are involved in the pathology of sarcoidosis. Exposures to insecticides, herbicides, bioaerosols, and agricultural employment are also associated with an increased risk for sarcoidosis. Due to its unknown etiology, early diagnosis and detection are difficult; however, the advent of advanced technologies, such as endobronchial ultrasound-guided biopsy, high-resolution computed tomography, magnetic resonance imaging, and 18F-fluorodeoxyglucose positron emission tomography has improved our ability to reliably diagnose this condition and accurately forecast its prognosis. This review discusses the causes and clinical features of sarcoidosis, and the improvements made in its prognosis, therapeutic management, and the recent discovery of potential biomarkers associated with the diagnostic assay used for sarcoidosis confirmation.
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              Sarcoidosis: a review for the internist

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                Author and article information

                Journal
                BMJ Case Rep
                BMJ Case Rep
                bmjcr
                bmjcasereports
                BMJ Case Reports
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                1757-790X
                2021
                7 June 2021
                7 June 2021
                : 14
                : 6
                : e239239
                Affiliations
                [1 ]departmentInternal Medicine , Dr Rajinder Prasad Government Medical College , Kangra, Himachal Pradesh, India
                [2 ]departmentInternal Medicine , Post Graduate Institute of Medical Education and Research , Chandigarh, India
                [3 ]departmentInternal Medicine , Army Hospital Research and Referral , New Delhi, Delhi, India
                [4 ]departmentDepartment of Radiotherapy and Oncology , IGMC , Shimla, Himachal Pradesh, India
                Author notes
                [Correspondence to ] Dr Kundan Mishra; mishrak20@ 123456gmail.com
                Author information
                http://orcid.org/0000-0002-6426-0309
                http://orcid.org/0000-0001-5754-0946
                Article
                bcr-2020-239239
                10.1136/bcr-2020-239239
                8186550
                34099443
                ca373595-814b-4303-a3e4-97167306565e
                © BMJ Publishing Group Limited 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 13 May 2021
                Categories
                Case Report
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                medical education,musculoskeletal syndromes
                medical education, musculoskeletal syndromes

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