Elsevier

Dermatologic Clinics

Volume 26, Issue 4, October 2008, Pages 439-445
Dermatologic Clinics

Erythema Induratum of Bazin

https://doi.org/10.1016/j.det.2008.05.007Get rights and content

Erythema induratum of Bazin is a chronic, nodular eruption that usually occurs on the lower legs of young women. It has been regarded as a manifestation of tuberculin hypersensitivity, a type of tuberculid occurring on the legs, whereas nodular vasculitis represents the nontuberculous counterpart. The number of reports of erythema induratum of Bazin is decreasing in most developed countries in accordance with the decreased incidence of tuberculosis. The etiopathogenesis of erythema induratum of Bazin and its relation to tuberculosis are still controversial, because mycobacteria cannot be cultured from the skin lesions. Most authors currently consider erythema induratum of Bazin (nodular vasculitis) a multifactorial disorder with many different causes, tuberculosis being one of them.

Section snippets

The concept of tuberculids

The concept of tuberculids was introduced by Jean Darier2 in 1896 to designate a group of dermatoses in individuals with a previous history of active TB who had a tuberculoid histopathology and presented with an intense reaction to tuberculin. All the bacteriologic methods that were available at that time for demonstrating a tuberculous origin (ie, cultures from cutaneous lesions demonstrating MTB) were negative. The tuberculids included initially lichen scrofulosum, papulonecrotic tuberculids,

Clinical features of erythema induratum of Bazin

Typical patients who present with EIB are usually young to middle-aged women. They present with recurrent flares of violaceous nodules or deep-seated plaques on the legs (Fig. 1).1, 6, 7, 8 The lesions are cold, are surprisingly not painful, and have a tendency to central ulceration. The superficial skin tends to show desquamation that forms a scaly collarette around the lesions or crusts overlying the ulcers. Most lesions resolve spontaneously within a few months, leaving postinflammatory

Pathology of erythema induratum of Bazin

EIB is a lobular panniculitis that shows a granulomatous inflammation with focal necrosis, vasculitis, and septal fibrosis in varying combinations.1, 6, 7, 8, 10 The histologic pattern greatly depends on the time that the biopsy was conducted during the disease evolution. The primary finding is a lobular panniculitis, sometimes showing a mixed pattern with septal and lobular inflammation (Fig. 2). The lobular inflammatory pattern can be initially focal, limited to the areas around a vessel, or

Historic evolution of the concept of erythema induratum of Bazin and its relationship with nodular vasculitis

Bazin11 first described EIB in 1855, a time when the tubercle bacillus had not yet been identified, as a condition occurring more frequently “on the legs of female laundresses and in young and plump, well-nourished women with the typical phenotype of those with scrofula.” Bazin11 classified EIB in the group of benign erythematous scrofulids, in which he included cuperosis, perniosis, and EIB. When MTB was discovered in 1882 and mycobacteria were found within cervical lymph nodes, the term

The relation of erythema induratum of Bazin with Mycobacterium tuberculosis infection

The causal relationship between EIB and TB has been based on a few circumstantial pieces of evidence in some patients, such as (1) a high degree of hypersensitivity to tuberculin skin testing in most patients,24, 25 (2) a frequent personal or family history of TB (the percentage of EIB patients with chest radiographic findings that suggest TB varies from 2% to 65%)24, 25, (3) presence of an active TB foci, (4) occasional coexistence with other tuberculids, such as papulonecrotic tuberculids or

Differential diagnosis

EIB can be easily mistaken for any of the diseases that produce chronic, nodular eruptions on the legs, including—but not limited to—erythema nodosum, cutaneous polyarteritis nodosa, sclerosing panniculitis, perniosis (chilblains), pancreatic paniculitis, lupus erythematosus profundus, and subcutaneous panniculitis-like T-cell lymphoma. A complete clinical history and physical examination are necessary in all cases. In many patients, performing an incisional biopsy with an adequate amount of

Diagnosis

The diagnosis of EIB is usually made on the basis of the characteristic clinical morphology, a positive tuberculin test, and circumstantial evidence of TB elsewhere in the body, supplemented by histopathologic findings. Detection of MTB DNA by PCR on the biopsy specimen further supports the diagnosis; however, failure to detect MTB by PCR does not exclude the diagnosis of EIB. For many dermatologists, the diagnosis can be confirmed by a good response to antituberculous treatment. In cases with

Treatment

In most patients who have EIB or NV, simple measures such as resting, using nonsteroidal anti-inflammatory drugs, and using compression stockings or supportive bandages can lead to complete remission of the lesions. In more severe cases, use of potassium iodide,40, 41 dapsone,22 colchicine,42 antimalarials, tetracyclines, gold salts,43 and prednisone can be successful in alleviating symptoms and inducing lesion remission, although they do not avoid late recurrences.

Many authors also favor

References (43)

  • B.E. Beyt et al.

    Cutaneous mycobacteriosis: analysis of 34 cases with a new classification of the disease

    Medicine

    (1981)
  • Y. Bureau et al.

    Les hypodermites nodulaires subaiguës des membres inférieurs

    Bull Soc Fr Dermatol Syphiligr

    (1958)
  • K.H. Cho et al.

    Erythema induratum of Bazin

    Int J Dermatol

    (1996)
  • J.W. Schneider et al.

    The histopathologic spectrum of erythema induratum of Bazin

    Am J Dermatopathol

    (1997)
  • E. Bazin

    Leçons théoriques et cliniques sur la scrofule

    (1861)
  • C.H. Audry

    Étude de la lésion de l'érythème induré (de Bazin): sur la notion ddu lymphatisme

    Ann Dermatol Syphiligr (Paris)

    (1898)
  • A. Whitfield

    On the nature of the disease known as erythema induratum scrofulosorum

    Am J Med Sci

    (1901)
  • A. Whitfield

    A further contribution to our knowledge of erythema induratum

    Br J Dermatol

    (1905)
  • J. Galloway

    Case of erythema induratum giving no evidence of tuberculosis

    Br J Dermatol

    (1913)
  • E.D. Telford

    Lesions of the skin and subcutaneous tissue in diseases of the peripheral circulation

    Arch Dermatol Syph

    (1937)
  • H. Montgomery et al.

    Nodular vascular diseases of the legs: erythema induratum and allied condition

    JAMA

    (1945)
  • Cited by (76)

    • Ulcerated, tender nodules of the lower extremities

      2022, JAAD Case Reports
      Citation Excerpt :

      Nodular vasculitis – Incorrect. Although this pathology also demonstrates erythematous, tender, ulcerated nodules of the lower extremities, its histopathology would reveal a mixed inflammatory infiltrate and would not demonstrate “ghost cells.”5 Factitial dermatitis – Incorrect.

    • Mass migration and climate change: Dermatologic manifestations

      2021, International Journal of Women's Dermatology
      Citation Excerpt :

      Various manifestations of CTB are summarized in Table 2. ( Barbagallo et al., 2002; Bellet and Prose, 2005; Choi et al., 2009; Dias et al., 2014; Fariña et al., 1995; Frankel et al., 2009; Handog et al., 2008; Jordaan et al., 1996; Machan et al., 2018; MacGregor, 1995; Marcoval et al., 1992; Mascaró and Baselga, 2008; Molpariya and Ramesh, 2017; Santos et al., 2014; Sehgal, 1994; Sharma et al., 2005; WHO, 2012; Wilson-Jones and Winkelmann, 1986; Yates and Ormerod, 1997). Dermatologic manifestations of climate change are myriad; however, the proliferation of infectious and communicable diseases is particularly troubling because they typically affect poor, vulnerable, and marginalized patients most severely.

    • Update on vasculitis: overview and relevant dermatological aspects for the clinical and histopathological diagnosis – Part II

      2020, Anais Brasileiros de Dermatologia
      Citation Excerpt :

      The assessment of patients with suspected NV should include the search for fragments of M. tuberculosis DNA in tissue samples using PCR, chest radiography, tuberculin skin test, and serology for HBV and HCV. Evidence of active systemic tuberculosis is rare.55,56 In most cases, cutaneous vasculitis has a self-limiting course.

    View all citing articles on Scopus
    View full text