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Phys Topicsdermatological

Phys · dermatological

Erythema Nodosum AND Panniculitis

Also known as Erythema Nodosum AND Panniculitis · erythema nodosum and panniculitis · septal panniculitis · lobular panniculitis · erythema induratum · nodular vasculitis · Weber-Christian disease · pancreatic panniculitis · lipodermatosclerosis

Consultant-physician depth guide to erythema nodosum and the panniculitides for FRACP DWE/DCE — septal vs lobular classification, Löfgren syndrome, erythema induratum and tuberculosis, alpha-1 antitrypsin deficiency panniculitis, pancreatic panniculitis, Weber-Christian disease, lipodermatosclerosis, biopsy interpretation, drug and infection triggers, corticosteroid and dapsone dosing, and the multisystem workup the examiner expects. Structured for FRACP DWE/DCE, MRCP and ABIM preparation.

medium12 referencesUpdated 26 July 202615 min readVerification in progress

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FRACP DWEFRACP DCEMRCP Part 2ABIM Internal Medicine

Red flags

  • Panniculitis with systemic upset, ulceration, necrosis or rapid expansion is not benign erythema nodosum — biopsy before labelling, and exclude pancreatic panniculitis, alpha-1 antitrypsin deficiency panniculitis and infectious nodular vasculitis
  • Erythema nodosum with bilateral hilar lymphadenopathy, fever and arthropathy is Löfgren syndrome — a clinical diagnosis of sarcoidosis that does not require biopsy but does require exclusion of tuberculosis before steroids
  • Erythema induratum (nodular vasculitis) is a paucibacillary tuberculous reaction in many populations — investigate and treat active or latent tuberculosis
  • Pancreatic panniculitis may precede the diagnosis of pancreatitis or pancreatic carcinoma — send lipase, amylase and image the pancreas in any neutrophilic, ulcerating panniculitis
  • Chronic recurrent panniculitis with fever and cytopaenia is the historical Weber-Christian pattern — re-classify with modern histology and molecular testing rather than accepting the label
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FRACP DWEFRACP DCEMRCP Part 2ABIM Internal Medicine

Red flags

  • Panniculitis with systemic upset, ulceration, necrosis or rapid expansion is not benign erythema nodosum — biopsy before labelling, and exclude pancreatic panniculitis, alpha-1 antitrypsin deficiency panniculitis and infectious nodular vasculitis
  • Erythema nodosum with bilateral hilar lymphadenopathy, fever and arthropathy is Löfgren syndrome — a clinical diagnosis of sarcoidosis that does not require biopsy but does require exclusion of tuberculosis before steroids
  • Erythema induratum (nodular vasculitis) is a paucibacillary tuberculous reaction in many populations — investigate and treat active or latent tuberculosis
  • Pancreatic panniculitis may precede the diagnosis of pancreatitis or pancreatic carcinoma — send lipase, amylase and image the pancreas in any neutrophilic, ulcerating panniculitis
  • Chronic recurrent panniculitis with fever and cytopaenia is the historical Weber-Christian pattern — re-classify with modern histology and molecular testing rather than accepting the label

Erythema Nodosum AND Panniculitis — Nodules of the Lower Limb

The answer first

Erythema nodosum and panniculitis are inflammatory reactions of the subcutaneous fat that present as tender nodules, most often on the shins. The single most important physician action is to separate the common, self-limiting septal pattern (classic erythema nodosum) from the lobular, ulcerating, systemic patterns that demand biopsy and a multisystem workup. [1]

A consultant-grade answer rests on four pillars: [1]

  1. Classify the nodules by where the inflammation sits. Erythema nodosum is the prototype septal panniculitis with spared lobules and no vasculitis; everything that ulcerates, scars, suppurates or recurs sits in the lobular group and behaves differently. The clinical pattern predicts histology, but histology — a 5 to 6 mm punch or incisional biopsy reaching subcutaneous fat — changes management. [4]
  2. Treat erythema nodosum as a reactive pattern, not a disease. In adults the dominant triggers are streptococcal pharyngitis, sarcoidosis (especially Löfgren syndrome), inflammatory bowel disease, pregnancy and drugs (oral contraceptives, sulfonamides, bromides, BRAF inhibitors); a focused history and a short panel resolve most cases without skin biopsy. [1]
  3. Recognise the dangerous mimics. Erythema induratum (nodular vasculitis) signals tuberculosis; pancreatic panniculitis may be the first clue to pancreatitis or pancreatic carcinoma; alpha-1 antitrypsin deficiency panniculitis ulcerates after minor trauma and demands specific replacement or avoidance of dapsone. [4]
  4. Stage treatment by severity and cause. Most erythema nodosum resolves in three to six weeks with rest, compression and non-steroidal anti-inflammatory drugs; refractory or relapsing disease warrants a short course of potassium iodide 300 to 900 mg three times daily, or oral corticosteroid (prednisone 0.5 to 1 mg/kg per day) once infection is excluded. [1] [2]

DWE high-yield: "Ulcerating panniculitis is not erythema nodosum." The triad that should send the patient to biopsy rather than reassurance is ulceration, recurrence and systemic symptoms — these three pivot the diagnosis from benign septal erythema nodosum to the lobular mimics (erythema induratum, pancreatic, alpha-1 antitrypsin deficiency, Weber-Christian) that need a defined systemic workup. [4]

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References12ShowHide
  1. [1]Ioannou P, Andrianaki AM, Dimopoulou D, et al. Clinical Characteristics of Patients with Erythema Nodosum and Risk of Relapse - a 17-Year Study. Maedica (Bucur), 2022.PMID 36032615
  2. [2]Leung AKC, Leong KF, Lam JM Erythema nodosum. World J Pediatr, 2018.PMID 30269303
  3. [3]Laborada J, Cohen PR Tuberculosis-Associated Erythema Nodosum. Cureus, 2021.PMID 35004007
  4. [4]Gilchrist H, Patterson JW Erythema nodosum and erythema induratum (nodular vasculitis): diagnosis and management. Dermatol Ther, 2010.PMID 20666819
  5. [5]Mascaró JM Jr, Baselga E Erythema induratum of bazin. Dermatol Clin, 2008.PMID 18793975
  6. [6]Franciosi AN, Ralph J, O'Farrell NJ, et al. Alpha-1 antitrypsin deficiency-associated panniculitis. J Am Acad Dermatol, 2022.PMID 33516773
  7. [7]Guo ZZ, Huang L, Huang YA, et al. Pancreatic panniculitis in acute pancreatitis. J Dig Dis, 2014.PMID 24620854
  8. [8]Dahl PR, Su WP, Cullimore KC, Dicken CH Pancreatic panniculitis. J Am Acad Dermatol, 1995.PMID 7657863
  9. [9]Kirresh O, Schofield J, George G Acute sarcoidosis: Löfgren's syndrome. Br J Hosp Med (Lond), 2015.PMID 25761805
  10. [10]Wanat KA, Rosenbach M Cutaneous Sarcoidosis. Clin Chest Med, 2015.PMID 26593142
  11. [11]Miteva M, Romanelli P, Kirsner RS Lipodermatosclerosis. Dermatol Ther, 2010.PMID 20666825
  12. [12]White JW Jr, Winkelmann RK Weber-Christian panniculitis: a review of 30 cases with this diagnosis. J Am Acad Dermatol, 1998.PMID 9674398

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