Video: Every Case Tells a Story| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • QA/QI
    • Technology
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

Fellow’s Forum Case Report: New Sarcoidosis Cases in Patients Treated with Tumor Necrosis Factor–Alpha Inhibitors

Jonida Cote, DO, Thomas Harrington, MD, Alicia Meadows, DO, Fan Lin, MD, and Androniki Bili, MD, MPH  |  Issue: November 2013  |  November 1, 2013

Although the patient remained asymptomatic, approximately one year later, a new chest CT study showed enlargement of existing mediastinal and hilar lymph nodes and new additional mediastinal nodes. Etanercept was discontinued due to a suspicion that it may be related to the relapse of sarcoidosis, and sulfasalazine was started in conjunction with a prednisone taper. Two months after discontinuation of etanercept, another chest CT showed decrease in size of the subcarinal lymph node and the right paratracheal nodes. PFTs showed a stable vital capacity of 77%, DLCO 59%, and forced expiratory volume (FEV1) was normal at 86% of predicted.

While on sulfasalazine, the patient was able to cope with his skin and joint disease. Intermittent joint flares were treated with intraarticular corticosteroid injections while psoriasis flares were treated with topical corticosteroids.

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

Two years later, the patient developed dyspnea on exertion and a nonproductive cough. PFTs showed a decrease in the vital capacity to 71% and DLCO to 55% of predicted. FEV1 decreased to 77% of predicted. This time, chest CT imaging showed improvement in mediastinal and hilar adenopathy, but there was an increase in parenchymal manifestations of sarcoid disease with perilymphatic distribution of nodules in upper lobes of lungs bilaterally. A bronchoscopy with biopsy was performed and excised tissue was consistent with noncaseating granulomas (see Figure 2). Repeat AFB and fungal cultures were negative. Serum calcium was 9.1(8.3–10.5 mg/dl) and angiotensin-converting enzyme (ACE) 49 (9–67 U/L). Because of his poorly controlled sarcoidosis, the patient was started on infliximab 300 mg intravenously every eight weeks. Four months later, the patient was free of respiratory, skin, and joint symptoms. He continues to do well and denies any dyspnea on exertion or other systemic manifestations of sarcoid disease while on infliximab. The pulmonary function tests are stable. The chest radiograph appearance has improved and his exercise tolerance improved.

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE
Fine needle aspiration of right hilar lymph node at bronchoscopy
Figure 3: Fine needle aspiration of right hilar lymph node at bronchoscopy. A mixed population of lymphocytes and granulomatous inflammation and multiple nucleated giant cells are present (Papanicolaou-stained direct smear x400).

Case #2

A 32-year-old white male with a history of psoriasis diagnosed in 1998 presented to rheumatology clinic in 2007 with a two-week history of pain and swelling in his hands, ankles, shoulders, and low back. Physical exam revealed erythematous plaques covered by silvery white scaly lesions over his lower extremities and there was onycholysis in several fingernails. There was an asymmetric synovitis involving his wrists, metacarpophalangeal and proximal interphalangeal joints, and both ankles. He was diagnosed with psoriatic arthritis and started on prednisone and methotrexate. A baseline CXR was unremarkable. After one month of treatment with methotrexate, the dose was reduced because of elevated serum transaminases, and the prednisone dose was increased due to persistent arthritis. This regimen offered only moderate disease control and it resulted in significant weight gain. Adalimumab 40 mg subcutaneously every other week was initiated.

Page: 1 2 3 4 5 | Single Page
Share: 

Filed under:ConditionsOther Rheumatic ConditionsPsoriatic Arthritis Tagged with:Psoriatic ArthritisSarcoidosisTherapiesTreatmentTumor Necrosis Factor–Alpha Inhibitor

Related Articles

    Case Report: Pulmonary Sarcoid-Like Reaction in Patient Treated with Etanercept

    April 15, 2022

    Sarcoidosis is a multisystem disease characterized by noncaseating granulomas in affected tissues, mostly involving the lungs and lymph nodes.1,2 The etiology of sarcoidosis remains unknown but is thought to be due to an inflammatory response to an antigen exposure in genetically predisposed individuals.1 Tumor necrosis factor-α (TNF‑α), a pro-inflammatory cytokine, plays an essential role in…

    Case Report: Sarcoidosis in Patient with History of IgG4-Related Disease

    September 14, 2021

    Sarcoidosis and IgG4-related disease (IgG4-RD) are both immune-mediated, often multi-organ, diseases of uncertain etiology capable of presenting with diverse clinical manifestations. Many clinical features are common to both conditions, including hypergammaglobulinemia, the ability to form inflammatory masses and involvement of the lymph nodes, lacrimal glands, salivary glands, meninges and lungs. Although imaging modalities, such as…

    Sarcoidosis in the Spotlight: Screening, Treatment & More Insights into Sarcoidosis

    June 1, 2021

    An expert discussed the screening and treatment of sarcoidosis and drug-induced sarcoidosis-like reactions during the 2021 ACR State-of-the-Art Clinical Symposium.

    Update on Extrapulmonary Sarcoidosis

    December 6, 2021

    Neurosarcoidosis & sarcoid dermatopathology are discussed.

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences