Erythema Nodosum


Article Author:
Wissem Hafsi


Article Editor:
Talel Badri


Editors In Chief:
Laurie Graham
Andrew Wilt
Mary Cataletto


Managing Editors:
Avais Raja
Orawan Chaigasame
Carrie Smith
Abdul Waheed
Khalid Alsayouri
Trevor Nezwek
Radia Jamil
Patrick Le
Anoosh Zafar Gondal
Saad Nazir
William Gossman
Hassam Zulfiqar
Steve Bhimji
John Shell
Matthew Varacallo
Heba Mahdy
Ahmad Malik
Sarosh Vaqar
Mark Pellegrini
James Hughes
Beata Beatty
Nazia Sadiq
Hajira Basit
Phillip Hynes
Tehmina Warsi


Updated:
5/2/2019 9:43:29 PM

Introduction

Erythema nodosum (EN) is a common acute nodular septal panniculitis, characterized by the sudden onset of erythematous, firm, solid, deep nodules or plaques that are painful on palpation and mainly localized on extensor surfaces of the legs. These nodules are characterized by a typical histological appearance regardless of the etiology, marked by acute inflammation of the dermo-hypodermic junction and interlobular septa of the hypodermic fat, evolving without necrosis or sequelae.[1][2][3]

Erythema nodosum is an acute, or recurrent hypersensitivity reaction to a variety of antigens with a clear female predominance that may be associated with several different stimuli or pathological conditions.

Etiology

Erythema nodosum can occur due to a vast number of underlying causes including but not limited to idiopathic, infectious, and a variety of noninfectious causes as outlined below.[4][5][6][7]

Idiopathic: No obvious etiology have been found in about 30% to 50% of published cases

Infections:

Bacterial:

  • Streptococcal infections-most common infectious etiology commonly streptococcal pharyngitis(28-48%)
  • Tuberculosis
  • Leprosy
  • Yersinia species (in Europe), salmonella, campylobacter gastroenteritis
  • Mycoplasma pneumonia
  • Tularemia
  • Cat scratch disease (Bartonella species)
  • Leptospirosis
  • Brucellosis
  • Psittacosis
  • Chlamydia trachomatous
  • Lymphogranuloma venereum

Viral:

  • Infectious mononucleosis
  • Hepatitis B, Hepatitis C
  • Human immunodeficiency virus(HIV)
  • Herpes simplex virus(HSV)
  • Epstein-Barr virus(EBV)
  • Para vaccinia

Fungal:

  • Coccidioidomycosis
  • Histoplasmosis
  • Blastomycosis

Parasitic:

  • Amebiasis
  • Giardiasis

Non infectious causes

Drugs

  • Antibiotics- penicillins, sulfonamides
  • Miscellaneous drugs- Oral contraceptives, bromides, iodides, TNF-alpha inhibitor

Malignancy

  • Leukemia
  • Lymphoma
  • Occult malignancies

Inflammatory Bowel Disease

  • Crohn's disease
  • Ulcerative colitis

Miscellaneous:

  • Sarcoidosis-Lofgren's syndrome(triad of erythema nodosum, acute arthritis, and hilar lymphadenopathy)
  • Pregnancy
  • Whipple disease
  • Behcet disease

Epidemiology

EN is the most common clinical form of the acute nodular hypodermis.  It occurs more often in women between 25 and 40 years, but it can be observed at any age. Compared to men, women are affected three to six times more. It is rare without sex predominance in the pediatric population. Of worldwide ubiquitous distribution, there is, however, an ethnic and geographical difference in the incidences explained by the variation of triggering etiological factors. Familial cases have been reported and are usually caused by an infectious etiology.

Pathophysiology

EN is the result of a nonspecific cutaneous reaction to various antigens. The mechanism involved would be immunologically mediated. Numerous direct and indirect evidence supports the notion of type IV delayed hypersensitivity response to many antigens. It is postulated that the pathogenesis may be due to deposition of immune complex in the venules of subcutaneous fat, production of oxygen free radicals, TNF-alpha and granuloma formation. However, this hypothesis is not accepted by all authors.

Histopathology

Skin biopsy is not usually needed in the typical forms as a diagnosis can be reached from a detailed history and physical examination. Usual features suggestive EN include acute onset tender nodules on typical locations(most commonly on shins).

Skin biopsy is useless in typical forms. It is indicated in cases of unusual topography, the persistence of nodules several weeks, fistulization or atrophic scarring, and/or livedoid disposition of nodules. It highlights the involvement of interlobular septa by a lymphohistiocytic inflammatory infiltrate, sparing fat lobules and vessels. This aspect is invariable, whatever the etiology.

History and Physical

EN is characterized in a rather stereotyped way, whatever its cause, by the following evolutionary aspects:

Prodromal Phase

  • Nonspecific from 3 to 6 days
  • Marked by fever, joint, and sometimes abdominal pain.
  • Often a picture of infection nasopharyngeal, with a slight alteration of the general condition.

Stade Phase

  • Settles quickly in 1 to 2 days.
  • The general syndrome occurs with fever, and arthralgia of the prodromal phase persists or increases.
  • Nodules appear on the extended faces of the legs and knees, and sometimes thighs and forearms. 
  • Nodules are small, 3 to 6, sometimes more, bilateral, roughly symmetrical, and spontaneously painful;
  • Clinical examination allows specifying the characters of the knots: 10 to 40 mm diameter; warm and firm on palpation, which accentuates their painful character; mobile in relation to the deep planes.
  • The pain of the lesions is exacerbated by orthostatism, which leads the patient to spontaneously seek the lying position with raised legs.
  • An edema of the ankles is often present.

Regressive Phase

  • Evolution is spontaneous but may be accelerated by rest or treatment symptomatic.
  • Each nodule evolves in ten days, taking blue and yellowish contusiform aspects, towards complete disappearance without sequelae.

EN never involves necrosis, ulceration, or scarring. It often evolves in several outbreaks, favored by orthostatism, and spreading out, at worst, over 4 to 8 weeks. The succession of outbreaks confers on the eruption a polymorphic appearance with knots of different ages, featuring the various shades of local biligenia.

Evaluation

The positive diagnosis of EN is primarily clinical. However, a thorough anamnesis (looking for tuberculous contagion, fever, bloody diarrhea, abdominal pain, respiratory problems, dysphagia, etc.) should be conducted as well as a complete clinical examination, always looking for associated signs.

In typical cases, a complementary investigation for positive diagnostic is not necessary. Nevertheless, it finds its place in the etiological diagnosis. Taking into account the above, the etiological assessment of an EN should include examinations according to the clinical orientation:

  • Blood count, vital signs, and C-reactive protein (in case of infectious context),
  • Mantoux + chest x-ray + interferon-gamma blood test (in case of tuberculous contagion or suspicion of Löfgren syndrome),
  • Throat smear + culture + rapid test - serology: anti-streptolysin O and streptodornase (in case of streptococcal suspicion),
  • Viral serology, two samples at four-week intervals (in case of suspicion of virosis),
  • Stool and stool examination (in case of diarrhea or digestive symptoms)
  • Cutaneous biopsy in atypical cases or in case of doubt.

Treatment / Management

Extended rest is desirable and may require a work stoppage. Analgesics are prescribed on request. Venous compression reduces the pain felt in orthostatism. Steroidal anti-inflammatory drugs, colchicine (1 to 2 mg/day), may be prescribed until symptoms improve. Etiologic treatment is essential in some cases, and antibiotic therapy is needed in case of streptococcal infection or anti-tuberculosis treatment. In the case of Löfgren syndrome, pulmonary radiographic monitoring is recommended, because if mediastinal adenopathies disappear in a few months in most patients, sarcoidosis may persist in 10% of cases.[8][9]

Differential Diagnosis

  • Non-suppurative infectious dermphypodermitis diagnosis is easy
  • Nodular hypodermitis with vascular involvement (periarteritis nodosa, and superficial thrombophlebitis) and damage to deep vessels of medium to sometimes large diameter is associated with hypodermic septal or lobular involvement. Nodules can become necrotic. The diagnosis is primarily histological.
  • Lobular hypodermitis or panniculitis involves lesions that are primarily greasy. The diagnosis is primarily histological, hence the absolute need for biopsy control. Several entities have been distinguished. The nodules can liquefy, fistulate, and leave a scar.

Pearls and Other Issues

EN is a noisy but benign syndrome, with a spontaneously favorable course, which is related to an underlying condition that needs to be diagnosed by clinical examination and some complementary oriented tests. In addition to symptomatic treatment, that of the underlying condition may be necessary.

Enhancing Healthcare Team Outcomes

EN is often encountered by primary care providers and nurse practitioners. While the diagnosis is clinical in most cases, sometimes a biopsy may be required to rule out another disorder. Healthcare workers should seek a consult with a dermatologist if there is any doubt about the diagnosis. The type of laboratory work up depends on the suspected cause. While EN may be painful, it is a benign disorder that usually remits spontaneously. If the primary disorder is not managed, EN may persist for months or even years. (Level V)

 

 


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Erythema Nodosum - Questions

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Which of the following skin diseases is seen with sarcoidosis?



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A 10-year-old female presents with painful, erythematous nodules located on the anterior lower legs. What is the most likely cause?



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Which of the following is an acute inflammatory reaction of the subcutaneous fat?



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Erythema Nodosum - References

References

Roth N,Biedermann L,Fournier N,Butter M,Vavricka SR,Navarini AA,Rogler G,Scharl M, Occurrence of skin manifestations in patients of the Swiss Inflammatory Bowel Disease Cohort Study. PloS one. 2019;     [PubMed]
Morgado F,Batista M,Coutinho I,Cardoso JC,Tellechea Ó, Erythema nodosum and sarcoid granulomas - letting the cat out of the bag. Dermatology online journal. 2018 Dec 15;     [PubMed]
Choi ME,Lee KH,Won CH,Chang SE,Lee MW,Choi JH,Lee WJ, A case of erythema nodosum-like panniculitis induced by nivolumab in a patient with oesophageal cancer. The Australasian journal of dermatology. 2019 Jan 17;     [PubMed]
Fujikawa T,Senoo A, Recurrent Erythema Nodosum as a Warning of Tuberculous Lymphadenitis. Mayo Clinic proceedings. 2019 Jan;     [PubMed]
Algahtani H,Shirah B,Marghalani S,Algarni A, Erythema nodosum in a patient with multiple sclerosis on dimethyl fumarate. Multiple sclerosis and related disorders. 2018 Dec 25;     [PubMed]
Porges T,Shafat T,Sagy I,Zeller L,Bartal C,Khutarniuk T,Jotkowitz A,Barski L, Clinical, Epidemiological, and Etiological Changes in Erythema Nodosum. The Israel Medical Association journal : IMAJ. 2018 Dec;     [PubMed]
Hanami Y,Mori T,Kikuchi N,Yamamoto T, Association of pyoderma gangrenosum, erythema nodosum and aseptic liver abscess without significant underlying disease. Clinical and experimental dermatology. 2018 Nov 20;     [PubMed]
Leung AKC,Leong KF,Lam JM, Erythema nodosum. World journal of pediatrics : WJP. 2018 Dec;     [PubMed]
Laroche A,Alarcon Chinchilla E,Bourgeault E,Doré MA, Erythema Nodosum as the Initial Presentation of Nivolumab-Induced Sarcoidosis-Like Reaction. Journal of cutaneous medicine and surgery. 2018 Nov/Dec;     [PubMed]

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