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Two Patients with Leprosy and the Sudden Appearance of Inflammation in the Skin and New Sensory Loss

  • Carlos Franco-Paredes ,

    Affiliations: Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America, Hospital Infantil de Mexico, Federico Gomez, Mexico City, Mexico

  • Jesse T. Jacob,

    Affiliation: Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America

  • Barbara Stryjewska,

    Affiliation: National Hansen's Disease Program, Baton Rouge, Louisiana, United States of America

  • Leo Yoder

    Affiliation: National Hansen's Disease Program, Baton Rouge, Louisiana, United States of America

Two Patients with Leprosy and the Sudden Appearance of Inflammation in the Skin and New Sensory Loss

  • Carlos Franco-Paredes, 
  • Jesse T. Jacob, 
  • Barbara Stryjewska, 
  • Leo Yoder

Leprosy is a chronic infection caused by Mycobacterium leprae that affects the peripheral nerves, skin, and potentially other organs [1][5]. Although the worldwide prevalence of leprosy has decreased in the era of multi-drug therapy (MDT), the global detection of new cases of leprosy remains a concern, with more than 250,000 new cases of leprosy reported in 2007 [3]. The precise mechanism of transmission of leprosy has not been conclusively defined; however, it is likely that this occurs through respiratory secretions by untreated borderline lepromatous and polar lepromatous cases [1],[5]. Target cells of infection are macrophages, histiocytes in the skin, and the nonmyelinating and myelinating Schwann cells in the peripheral nerve, leading to axonal dysfunction and demyelination [6]. Nerve injury plays a central role in the pathogenesis of leprosy, leading to functional impairment and deformity of hands and feet and the eyes [1],[6]. Leprosy is diagnosed by definite loss of sensation in a hypopigmented or reddish skin patch, a thickened peripheral nerve with loss of sensation and muscle weakness in the affected nerve, and presence of acid-fast bacilli on skin smear or biopsy [1],[4].

The immunological response to M. leprae mounted by the host will determine the different potential clinical states. The Ridley-Joplin system uses clinical and histopathological features and the bacteriologic index and includes the polar categories (lepromatous [LL] and tuberculoid [TT]) and the borderline states (borderline tuberculoid [BT], borderline borderline [BB], and borderline lepromatous [BL]) [1] (Table 1). In the polar tuberculoid category, a Th1 type cell–mediated immune response with a low bacterial load is seen. Lepromatous states are characterized by low cell-mediated immunity and a higher bacterial load [5] (Table 1). Clinically, patients with tuberculoid leprosy have a single or very few hypopigmented macules or plaques with a raised edge; they are dry, scaly, hairless, and have reduced sensation; and only a few peripheral nerves are commonly enlarged [1]. Lepromatous leprosy is characterized by widely and symmetrically distributed skin macules, nodules, erythematous papules, and diffuse skin infiltration; thickened peripheral nerves are more frequently identified. Borderline states represent a mixture of signs and symptoms of the polar categories [1].

Table 1. World Health Organization System and Ridley-Joplin Classification and Type of Reaction.

Description of Case A

A 31-year-old Brazilian male living in the United States for the previous four years presented with progressive crops of new nontender nodules on all four extremities over a 16-month period (Figures 1 and 2). He had more than ten nodules in each limb, with some reaching 0.5–1.0 cm in diameter. A 3×5-cm area of diffuse skin infiltration was present in his left thigh. He had referred numbness in the lower extremities. He had thickened bilateral ulnar nerves with mild sensory loss by monofilament testing in the ulnar nerve and peroneal nerve territories without any nerve tenderness identified. His posterior tibial nerves were also palpable. There was no muscle weakness identified by voluntary muscle testing using the 0–5 modified Medical Research Council scale. Nasal mucosa was normal. Eyelid closure was tested and there was no evidence of lagopthalmos; eyelashes were normal. His conjunctivae were pink. A skin biopsy demonstrated a diffuse lymphocytic infiltrate with multiple foamy macrophages. Fite-Faraco staining showed multiple acid-fast bacilli (Figure 3). A skin smear demonstrated a bacterial index (BI) of 5. The patient was diagnosed with lepromatous leprosy, using the Ridley-Joplin staging system [1], or multibacillary leprosy per the World Health Organization (WHO) staging [2][5] (Table 1). He was started on MDT consisting of dapsone 100 mg PO daily, rifampin 600 mg PO daily, and clofazimine 50 mg PO daily. (In the United States, the National Hansen's Disease Program recommends using daily rifampin, while the rest of the world uses rifampin once monthly with less than 1% relapses [4].)

Figure 3. Fite-Faraco staining of skin biopsy demonstrating abundant acid-fast bacilli inside foamy macrophages (arrow).

We recommended that he continue his MDT until his BI (the BI is a logarithmic scale used to assess response to MDT in skin smears) decreased below 2 (dead bacteria may be present in the skin up to 10 years). Despite the WHO recommendation of 12 months of MDT for multibacillary cases such as our patient, many experts still advocate 24 months of MDT for patients with a BI >4 at diagnosis [1].

Six months after the initiation of MDT, patient A experienced the abrupt onset of multiple new erythematous and ulcerated skin nodules (1–2 cm) distributed in the upper limbs, trunk, and right leg (Figure 4). The original leprosy nodules remained as they were. He also had a fever up to 39.5°C, swelling of his hands and feet, and cervical lymphadenopathy. He had thickened bilateral ulnar and peroneal nerves with moderate sensory loss by monofilament testing compared to his initial baseline evaluation in the ulnar nerve and peroneal nerve territories. There was no nerve tenderness identified. There was no muscle weakness identified by voluntary muscle testing. Histopathological examination of one new lesion showed evidence of neutrophilic infiltration. He had no clinical evidence of uveitis, arthritis, or orchitis.

Figure 4. Newly appeared and rapidly ulcerating lesion in the right arm, accompanied with fever, cervical lymphadenopathy, and malaise.

Based on the clinical history and signs, our patient was diagnosed with a type 2 leprosy reaction [5] (Table 2). He was treated with 60 mg of oral prednisone daily tapered over a 12-week period [4]. A 6-week course of thalidomide 200 mg PO daily was also used due to the severity of the reaction, with rapid clinical improvement (Table 3). His rifampin dose was reduced to 600 mg monthly due to the concomitant use of prednisone since rifampin may lower prednisone serum levels. Our patient presented a protracted course with two more episodes of severe type 2 reactions that were treated with a similar corticosteroid regimen. A repeat skin biopsy performed 12 months after commencing MDT showed decreasing numbers of acid-fast bacilli, and skin smears showed a decreasing BI.

What Are Leprosy Reactions and How Are They Diagnosed?

Reactional states represent a change in the immunological state of a patient with leprosy. These reactions are characterized by inflammatory episodes of the skin, nerves, and other organs that can occur anytime within the course of leprosy, but are often observed after starting treatment, and can result in irreversible nerve damage [2],[4]. There are two main types of reactions: type 1, or reversal reactions (RR), and type 2 reactions, or erythema nodosum leprosum (ENL) [5] (Table 2).

Type 1 reactions are considered to be an upgrading in the cell-mediated immune response to M. leprae [5]. These patients have relatively few bacteria and low antibody levels to M. leprae as compared to lepromatous states [1]. Schwann cells have been shown to express Toll-like receptor 2 (TLR-2) and major histocompatiblity complex (MHC II) with antigen presentation ability, resulting in CD4+ T cell activation [1],[7]. The incidence of type 1 reactions occurring as immune-reconstitution syndromes among patients with borderline leprosy co-infected with HIV/AIDS receiving antiretroviral therapy supports an upgrading of cell-mediated immunity as a key pathogenic event in type 1 reactions [8].

Type 2 reactions are characterized by an inflammatory infiltrate of neutrophils with associated vasculitis and/or panniculitis [9]. Although it is accepted that a cell-mediated component is required, the ultimate pathogenesis results from deposition of antigen–antibody complexes in tissues, leading to an acute inflammatory response, particularly in nerves, skin, and other organs with increased levels of circulating TNF-α and IL-6 [9]. The major T cell subtype identified during type 2 reactions is the CD4+ lymphocyte subset [9].

Type 1 reactions affect patients within the borderline spectrum (BT, BB, and BL), while type 2 reactions occur among patients with BL and LL states [5] (Tables 1 and 2). The higher the bacterial load and the greater the infiltration of the skin, the higher the risk of developing type 2 reactions [1],[8]. For type 1 reactions, starting MDT is considered the strongest risk factor [1].

In the MDT era, reactions occur in approximately 15%–39% of patients with leprosy [10][12].

How Do Type 2 Reactions Present Clinically?

The diagnosis of leprosy reactions is based primarily on clinical history and examination [1],[5]. Type 2 reactions present with crops of new tender subcutaneous nodules sometimes associated with fever, malaise, arthralgias, neuritis, and adenopathy, and occasionally uveitis, orchitis, or dactylitis [1],[2],[5] (Table 2). Type 2 reactions usually occur after a patient with leprosy has been on MDT for months or years. Histologically, skin biopsy specimens may demonstrate a mixed dermal infiltrate of neutrophils and lymphocytes and fragmented bacilli in macrophages [2],[5],[13].

Type 2 reactions often follow a protracted clinical course [13]. In fact, three subtypes of type 2 reactions have been identified depending on its clinical course: acute single episode, multiple acute episodes, and chronic. Most cases tend to become chronic [13].

What Is the Optimal Management of Type 2 Reactions?

MDT should be continued concomitantly to anti-reaction drugs in type 1 and type 2 reactions. In those who have completed MDT, management of reactions does not require restarting MDT [2]. For mild reactions, non-steroidal anti-inflammatory agents may be used (Table 3) [5]. Corticosteroids (prednisone or prednisolone) remain the standard of care for the acute symptoms of severe type 2 reactions with daily regimens tapered over a 12-week course [1],[2],[4],[5]. However, many patients require repeated treatment for multiple acute episodes or long-term corticosteroid use [2],[13].

Thalidomide is sometimes used in combination with corticosteroids for controlling severe type 2 reactions [10]. Its therapeutic effect has been associated with transient immune stimulation of IL-2 and interferon-γ produced by activated CD4+ and CD8+ lymphocytes [14]. Nonetheless, thalidomide has significant limitations for widespread use: it is costly, unavailable in many settings, and has significant side effects (teratogenicity, sedation, neuropathy, and thrombosis) [4].

Clofazimine is considered an anti-reaction agent in addition to its role in MDT against M. leprae (Table 3). Management of type 2 reactions with clofazimine is indicated in patients who are not responding satisfactorily to treatment with corticosteroids or when the risk of toxicity with corticosteroids is high [2]; or as monotherapy when corticosteroids are contraindicated [4]. The total duration of treatment with high dose clofazimine should not exceed 12 months. Side effects of clofazimine include gastrointestinal symptoms and skin hyperpigmentation [2],[4].

The use of tumor necrosis factor inhibitors (TNF-α inhibitors) has been considered in patients with type 2 reactions. However, the TNF-α inhibitor infliximab has been associated with the clinical development of leprosy and, upon its discontinuation, the occurrence of type 1 reactions [15]. The effects of other TNF inhibitors are not known. Azathioprine has been successfully used in preventing recurrences [16]. Mycophenolate mofetil is not effective when used as a corticosteroid sparing agent [17].

Description of Case B

A 28-year-old Indian male, living in the United States for 2 years, presented with an 8-month history of multiple skin plaques that were well defined with their edges slightly raised, and scaly, and localized mostly in the face, upper and lower limbs, and trunk (Figure 5A). Some of these plaques were anesthetic and dry. The lesions range from 2 cm to 6 cm in diameter, with the ones on the right thigh being the largest. No thickened peripheral nerves or nerve tenderness were identified. Monofilament testing demonstrated mild sensory loss, more in the right hand than the left, and mainly in the distribution of the ulnar nerve. There was no other sensory loss detected at other sites and there was no muscle weakness identified by voluntary muscle testing using the 0–5 modified Medical Research Council scale. Nasal mucosa was normal. There was no evidence of madarosis with normal eyelashes, corneal reflexes, and eyelid closure; his conjunctivae were pink. Fite-Faraco stains of skin biopsy taken from one of the lesions in the right elbow demonstrated acid-fast organisms within histiocytes and within nerve fibers. A diagnosis of borderline tuberculoid was made (Tables 1 and 2) and he began receiving MDT consisting of rifampin 600 mg once a month, dapsone 100 mg daily, and clofazimine 50 mg daily.

Figure 5. Patient with a type 1 leprosy reaction.

(A) Patient with borderline tuberculoid leprosy with inflammation of previously existent skin plaques distributed in his four limbs and in the thorax. (B) Improvement of inflammation of the skin findings after corticosteroid treatment.

Almost 2 months after he began receiving MDT, he developed a sudden onset of bilateral lower limb edema, with inflammation of previously existent skin plaques distributed in his four limbs and in the trunk. No new skin lesions were identified (Figure 5A). He also developed neuropathic pain in his lower limbs. No thickened peripheral nerves or nerve tenderness were identified. Monofilament testing demonstrated worsening sensory loss in the distribution of the ulnar nerves, and new mild sensory loss in the peroneal nerve distribution bilaterally. His voluntary muscle testing remained normal. At this point, our patient was diagnosed with a type 1 reaction. Along with continuing his MDT, he received a corticosteroid regimen tapered over a 20-week period, resulting in significant improvement (Figure 5B). He completed a 6-month course of MDT and has finished his prednisone tapered over a 9-month period.

How Do Type 1 Reactions Present Clinically?

Type 1 reactions are characterized by increasing swelling, erythema, and tenderness of previously existing skin lesions accompanied by increased neuritis manifested as pain or tenderness in one or more nerves associated with pain and nerve function impairment [2],[5] (Table 2). Involvement of the face may result in facial paralysis and lagopthalmos; when affecting the eyes it may cause iritis and scleritis [5]. In type 1 reactions, some key features identified on skin biopsies include dermal edema, granuloma edema, and presence of giant cells and plasma cells [18].

What Is the Optimal Management of a Type 1 Reaction?

The foremost priority in the management of type 1 reactions is the treatment of neuritis followed by decreasing acute inflammation, easing pain, and reversing nerve and eye damage [1],[5]. Corticosteroids (prednisone or prednisolone) are the standard of care [1], [2][5]. WHO recommends a regimen of corticosteroids tapered over a 12-week period (Table 3) [4]. However, regimens of corticosteroids tapered over a longer period (20 weeks) have been shown to be more effective in controlling type 1 reactions [1]. The most commonly affected nerves are the facial, ulnar, median, common peroneal, facial, and posterior tibial.

If the reversal reaction becomes chronic, requiring high doses of corticosteroids for extended periods, adjunctive clofazimine, started at 100 mg three times daily and subsequently tapered over many months, may be used (Table 3) [5]. Cyclosporine-A and methrotexate may be effective in patients intolerant to corticosteroids [19],[20].

Discussion of Cases A and B

The clinical management of leprosy reactions is challenging. Leprosy reactions occur among patients with borderline and lepromatous leprosy and may occur prior to the initiation of MDT, during MDT, or even years after its completion. Corticosteroids are considered the standard of care for managing type 1 and type 2 reactions, sometimes in combination with clofazimine or thalidomide. Long-term follow-up of patients diagnosed with leprosy and who have suffered leprosy reactions is needed, even after completion of MDT. Further research regarding their pathogenesis and optimal medical management is warranted.

Key Learning Points

  • Leprosy reactions contribute significantly to neurological sequelae and functional and anatomical impairment.
  • Leprosy reactions occur among patients with borderline and lepromatous leprosy and may occur prior to the initiation of MDT, during MDT, or even years after its completion.
  • Early detection and effective treatment of reactions is critical to prevent nerve damage.
  • The treatment of choice for both types of reactions (and neuritis) is corticosteroids.

Supporting Information

Alternative Language Abstract S1.

Translation of the abstract into Spanish by Carlos Franco-Paredes


(0.03 MB DOC)


Both patients (cases A and B) signed written consents for publication. The study was approved by the Institutional Review Board of Emory University - IRB00006966 (Leprosy Reactions).


  1. 1. Walker SL, Lockwood DNJ (2006) The clinical and immunological features of leprosy. Brit Med Bull 77 and 78: 103–121.
  2. 2. World Health Organization (2006) Global Strategy for Further Reducing the Leprosy Burden and Sustaining Leprosy Control Activities 2006–2010. Operational guidelines. Geneva: World Health Organization.
  3. 3. World Health Organization (2006) Global leprosy situation, beginning of 2008. Wkly Epidemiol Rec 2008 33: 293–300.
  4. 4. World Health Organization (2003) The final push strategy to eliminate leprosy as a public health problem. Questions and answers. Second Edition. Geneva: World Health Organization.
  5. 5. Yoder LJ (1996) Management of reactions in Hansen's disease. The Star. Carville (Louisiana): Gillis W. Long Hansen's Disease Program.
  6. 6. Scollard DM (2008) The biology of nerve injury in leprosy. Lepr Rev 79: 242–253.
  7. 7. Misch EA, Macdonald M, Ranjit C, Sapkota BR, Wells RD, et al. (2008) Human TLR1 deficiency is associated with impaired mycobacterial signaling and protection from leprosy reversal reaction. PLoS Negl Trop Dis 2: e231. doi:10.1371/journal.pntd.0000231.
  8. 8. Deps PD, Lockwood DNJ (2008) Leprosy occurring as immune reconstitution syndrome. Trans R Soc Trop Med Hyg102: 966–968.
  9. 9. Kahawita IP, Lockwood DNJ (2008) Towards understanding the pathology of erythema nodosum leprosum. Trans R Soc Trop Med Hyg 102: 329–337.
  10. 10. Walker SL, Waters MF, Lockwood DN (2007) The role of thalidomide in the management of erythema nodosum leprosum. Lepr Rev 78: 197–215.
  11. 11. van Brakel WH, Nicholls PG, Das L, Barkataki P, Suneetha S, et al. (2005) The INFIR cohort study: investigating prediction, detection, and pathogenesis of neuropathy and reactions in leprosy. Methods and baseline results of a cohort of multibacillary leprosy patients in North India. Lepr Rev 76: 14–34.
  12. 12. van Brakel WH, Nicholls PG, Wilder-Smith EP, Das L, Barkataki P (2008) Early Diagnosis of neuropathy in leprosy—comparing diagnostic tests in a large prospective study (the INFIR cohort study). PLoS Negl Trop Dis 2: e212. doi:10.1371/journal.pntd.0000212.
  13. 13. Pocaterra L, Jain S, Reddy R, Muzaffarullah S, Torres O, et al. (2006) Clinical course of erythema nodosum leprosum: An 11-year cohort study in Hyderabad, India. Am J Trop Med Hyg 74: 868–879.
  14. 14. Haslett PA, Roche P, Butlin R, Macdonald M, Shrestha N, et al. (2005) Effective treatment of erythema nodosum leprosum with thalidomide is associated with immune stimulation. J Infect Dis 192: 2045–2053.
  15. 15. Scollard DM, Joyce MP, Gillis TP (2006) Development of leprosy and type 1 leprosy reactions after treatment with infliximab: A report of 2 cases. Clin Infect Dis 43: e19–e22.
  16. 16. Verma KK, Srivastava P, Minz A, Verma K (2006) Role of azathioprine in preventing recurrences in a patient of recurrent erythema nodosum leprosum. Lepr Rev 77: 225–229.
  17. 17. Burdick AE, Ramirez CC (2005) The role of mycophenolate mofetil in the treatment of leprosy reactions. Int J Lepr Other Mycobact Dis 73: 127–128.
  18. 18. Lockwood DNJ, Lucas SB, Desikan KV, Ebenezer G, Suneetha S, Nicholls P (2008) The histological diagnosis of leprosy type 1 reactions: identification of key variables and an analysis of the process of histological diagnosis. J Clin Pathol 61: 595–600.
  19. 19. Castro de Sena CB, Guedes Salgado C, Penabler Tavares CM, Vieira da Cruz CA, Xavier MB, et al. (2006) Cyclosporine A treatment of leprosy patients with chronic neuritis is associated with pain control and reduction in antibodies against nerve growth factor. Lepr Rev 77: 121–129.
  20. 20. Biosca G, Casallo s, Lopez-Velez R (2007) Methotrexate treatment for type 1 (reversal) leprosy reactions. Clin Infect Dis 45: e7–e9.