What are the typical clinical presentations of palpable lesions (nodules, plaques, and lymphadenopathy) in sarcoidosis?

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Clinical Presentation of Palpable Lesions in Sarcoidosis

Lumps from sarcoidosis present in distinct patterns: highly specific skin lesions like lupus pernio (chronic violaceous plaques on the nose, cheeks, and ears), subcutaneous nodules (firm, asymptomatic nodules under normal-appearing skin), maculopapular lesions (erythematous or violaceous raised bumps), and lymphadenopathy (most characteristically bilateral hilar nodes, but also palpable peripheral nodes). 1, 2

Specific Cutaneous Lesions (Granulomatous)

Lupus Pernio

  • Highly specific for sarcoidosis and represents chronic, disfiguring disease 1, 2
  • Presents as chronic violaceous skin lesions, typically on the nose, cheeks, and ears 2
  • Associated with more severe systemic involvement and chronic course 3
  • Hallmark of chronic disease that does not respond well to conventional treatments 4, 5

Subcutaneous Nodules

  • Present as firm, asymptomatic nodules covered by normal-appearing skin, most commonly on forearms and legs 1, 6
  • Diagnosis requires high index of suspicion since overlying skin appears normal 6
  • In the vast majority of patients (>70%), subcutaneous nodules are the manifestation that allows diagnosis of systemic sarcoidosis 6
  • Strong association with bilateral hilar lymphadenopathy (72.7% of cases) 6
  • More often associated with remission of systemic disease at two years compared to plaques or lupus pernio 4

Maculopapular Lesions

  • Appear as maculopapular, erythematous, or violaceous skin lesions 1, 2
  • Most frequent type of specific (granulomatous) skin lesions 4
  • Usually transient or tend to follow the course of systemic disease 5
  • Associated with better prognosis and more likely remission at two years 4

Plaques

  • Present as raised, flat-topped lesions 4, 5
  • Associated with chronic sarcoidosis and more severe systemic involvement 5, 3
  • Hallmark of chronic disease course 4

Lymphadenopathy

Thoracic Lymph Nodes

  • Bilateral hilar adenopathy is the most characteristic finding, present in approximately 90% of cases 2
  • Highly probable diagnostic feature on chest X-ray, CT, and PET imaging 1

Peripheral Lymphadenopathy

  • Two or more enlarged extrathoracic nodes visible on CT, MRI, or PET imaging 1
  • Palpable peripheral lymph nodes may be present 7

Other Palpable Organ Involvement

  • Symmetrical parotid gland enlargement presents as bilateral facial swelling 1, 2
  • Lacrimal gland swelling may be visible or palpable 1, 2
  • Hepatomegaly and/or splenomegaly may be detected on physical examination 1, 2

Non-Specific Lesions

Erythema Nodosum

  • Presents as tender, raised nodules on the shins 2
  • Highly probable indicator when part of Löfgren's syndrome (bilateral hilar adenopathy with erythema nodosum and/or periarticular arthritis) 1, 2
  • Associated with excellent prognosis and spontaneous resolution 4, 3
  • Does not show granulomas on biopsy, distinguishing it from specific lesions 4, 5

Critical Clinical Pearls

Prognostic significance varies dramatically by lesion type: Löfgren's syndrome and erythema nodosum indicate acute, benign disease with good prognosis, while lupus pernio and plaques signal chronic, severe disease requiring aggressive management 4, 5, 3

Skin biopsy of specific lesions reveals non-caseating granulomas, allowing early diagnosis through a minimally invasive procedure 4, 5

Cutaneous lesions occur in 9-37% of sarcoidosis patients, making skin the second most commonly involved organ after the lungs 5

Common Diagnostic Pitfalls

  • Failure to biopsy subcutaneous nodules because overlying skin appears normal, leading to missed diagnosis 6
  • Inadequate exclusion of infections (tuberculosis, fungal) that can mimic sarcoidosis exactly with granulomatous lymphadenopathy 2, 8
  • Insufficient workup for systemic disease when cutaneous sarcoid granulomas are identified—every patient requires systemic evaluation 3
  • Underestimating psychological impact of chronic disfiguring lesions like lupus pernio, which require treatment despite being minimally symptomatic physically 4, 5

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Clinical Signs of Sarcoidosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Skin manifestations of sarcoidosis.

Presse medicale (Paris, France : 1983), 2012

Research

Granulomatous cutaneous sarcoidosis: diagnosis, relationship to systemic disease, prognosis and treatment.

Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2013

Research

Sarcoidosis as a systemic disease.

Clinics in dermatology, 2014

Guideline

Sarcoidosis and Calcified Lymph Nodes

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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