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

10 Clinical Insights & Rheumatology Pearls Presented at ACR Convergence 2021

Mithu Maheswaranathan, MD  |  December 2, 2021

ACR Convergence 2021—On Nov. 7, attendees of the Rheumatology Secrets & Pearls session gained new insights into the diagnosis, management and treatment of an array of rheumatic diseases, from bread-and-butter conditions to rare clinical entities.

Jason Kolfenbach, MD, associate professor of medicine and ophthalmology and director of the Rheumatology Fellowship Program at the University of Colorado, Denver, led the popular session, along with John H. Stone, MD, MPH, professor of medicine at Harvard Medical School, and director of clinical rheumatology at Massachusetts General Hospital, Boston.

Dr. Kolfenbach

Dr. Kolfenbach explained that clinical pearls can be useful when randomized controlled trial data are not available for a particular question or when the data are available but don’t address a particular patient’s clinical scenario. Here are 10 pearls from their presentation. 

Vasculitis Pearls

1. Dr. Stone discussed a unique manifestation of anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis: strawberry gingivitis.1 “Strawberry-like gingivitis is a clue to the diagnosis of granulomatosis with polyangiitis [GPA],” he explained. These lesions are not always florid throughout the mouth, and they may be subtle. However, if present, they are “strongly suggestive” of GPA.

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

2. When evaluating a patient for a potential diagnosis of vasculitis, it is important to recognize that ANCA-associated vasculitis does not typically cause hard palate lesions, Dr. Kolfenbachexplained. ”Hard palate lesions should bring to mind malignancy or cocaine-induced destructive lesions,” he said.

A human neutrophil elastase (HNE) antibody test can be useful in this setting. This antibody is sometimes present in cocaine-induced midline lesions but not in ANCA-associated vasculitis. However, the assay is not available commercially.

Dr. Stone

3. Next, Dr. Stone discussed some pearls and myths related to Takayasu’s arteritis. He noted that immunosuppression is often not urgently needed in the treatment of Takayasu’s arteritis. This is, in part, due to the collateral circulation that often develops; patients with such collaterals are not at risk for limb-threatening ischemia.

“Stenting should be undertaken after careful thought and reconsideration because of exuberant collateral circulation that develops, making stenting irrelevant in most cases,” he explained.

One final pearl: Dr. Stone said to remember to listen for bruits on the patient’s back on both sides of the spine. “If you detect a bruit, it may have one of two origins: the pulmonary artery or the descending aorta,” he said.

Sarcoid Loves the Nasal Ala

4. Dr. Kolfenbach presented the case of a patient with atrophic skin changes over the cheeks that could be mistaken for discoid lupus. However, this patient had granulomatous changes due to lupus pernio (also called Besnier-Tenneson syndrome), a form of cutaneous sarcoidosis. Lupus pernio tends to present with violet-colored papules or plaques on the nose and cheeks, whereas discoid lupus tends to present with indurated plaques on the head and neck.

Page: 1 2 3 | Single Page
Share: 

Filed under:ACR ConvergenceConditionsGout and Crystalline ArthritisMeeting ReportsProfessional TopicsVasculitis Tagged with:ACR Convergence 2021C-reactive protein (CRP)Clinical PracticeGoutPractice PearlsVasculitis

Related Articles
    IgG4-Related Kidney Disease: Diagnostics, Manifestations, & More

    IgG4-Related Kidney Disease: Diagnostics, Manifestations & More

    May 17, 2018

    Immunoglobin G4-related disease (IgG4-RD) is a rare fibro-inflammatory disease of unknown etiology that has been recently recognized. It can cause fibro-inflammatory masses in almost every organ of the body and is associated with dense lymphoplasmacytic infiltration of IgG4-postitive plasma cells, storiform fibrosis and elevated levels of serum IgG4.1 IgG4-RD is a systemic disease that may…

    A Spotlight on IgG4-Related Disease

    January 1, 2013

    What rheumatologists need to know about identifying and diagnosing immunoglobulin G4-related disease (IgG4-RD)

    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…

    JNT Visual / shutterstock.com

    ACR/EULAR Release New Classification Criteria for IgG4-Related Disease

    January 16, 2020

    Immunoglobulin G4-related disease (IgG4-RD) can cause fibroinflammatory lesions in nearly any organ, and diagnosis is challenging. ACR/EULAR classification criteria for IgG4-RD have been developed and validated in a large cohort of patients. These criteria have performed well in tests and should contribute substantially to future clinical, epidemiologic and basic science investigations.

  • 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