Sarcoidosis



Sarcoidosis


Preston W. Chadwick and Warren R. Heymann


Evidence Levels:  A Double-blind study  B Clinical trial ≥ 20 subjects  C Clinical trial < 20 subjects  D Series ≥ 5 subjects  E Anecdotal case reports


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Sarcoidosis is a multisystem disease of unknown etiology characterized histologically by non-caseating granulomas. It is considered to be immune mediated, with a Th1-predominant cytokine profile. Skin manifestations are observed in approximately 25% of cases. Sarcoidosis has been reported to develop following exposure to inorganic particles in the environment. The use of polymerase chain reaction (PCR) techniques has also led to the identification of mycobacterial and propionibacterial DNA and RNA in sarcoidal tissue. Sarcoidosis may be the end result of immune responses to those or other specific triggers. Therapy for erythema nodosum associated with sarcoidosis is addressed in the chapter on erythema nodosum.



Management strategy


The treatment of cutaneous sarcoidosis depends on the type and extent of lesions present and is directed at suppressing the formation of granulomas. Guidelines for treating extracutaneous involvement can be found elsewhere, but it should be recognized that therapy for internal involvement may take precedence over skin disease and that response to treatment may be variable, depending on the type of tissue involved.


In small papular or extremely localized sarcoidosis, treatment with potent topical corticosteroids or intralesional triamcinolone acetonide (3.3–10 mg/mL) is reasonable. If this is ineffective or involvement is more diffuse, oral chloroquine (up to 3.5 mg/kg/day) or hydroxychloroquine (up to 6.5 mg/kg/day) may be effective in addition to methotrexate or tetracyclines. If no response is seen, or disfiguring lesions are present, oral prednisone can be used at a dose of 1 mg/kg daily (maximum 60 mg) for up to 3 months, and then tapered if improvement or a stable level is reached, to a maintenance dose of 5–10 mg on alternate days for several months. Periodic escalations in dose are necessary with flares of the disease.


Methotrexate may be used as a corticosteroid-sparing agent or as monotherapy in those patients with lupus pernio, ulcerative sarcoidosis, or severe disease that has not responded to prednisone. Initial doses of 15–20 mg weekly are favored. Mycophenolate mofetil has also shown promise as a steroid-sparing agent. Thalidomide, azathioprine, chlorambucil, isotretinoin, or allopurinol could be considered if methotrexate or mycophenolate mofetil fail in this subset of patients. Azathioprine and chlorambucil are better studied in patients with pulmonary sarcoidosis. Thalidomide seems to be more effective than isotretinoin and allopurinol in cutaneous disease. Reported failures are described with etretinate and allopurinol.


Biologic agents that inhibit tumor necrosis factor (TNF)-α are therapeutic modalities that should be considered in patients with lupus pernio, cutaneous sarcoidosis recalcitrant to systemic steroids or steroid sparing agents. Infliximab may be more effective than adalimumab, but may be associated with a higher rate of infection and autoimmune disease. Etanercept does not appear to be useful for the treatment of sarcoidosis; indeed some studies have reported on its potential role in patients developing sarcoidosis, or in relapse of pre-existing sarcoidosis.


Leflunomide and apremilast have shown promise in the treatment of cutaneous sarcoidosis unresponsive to other therapies, but further studies are needed to establish long-term usefulness.


Localized disease that does not respond to topical or intralesional corticosteroids, or in those cases in which the use of systemic antimalarial drugs or corticosteroids is undesirable, may represent a niche for other modalities, such as excision, laser, photodynamic therapy, PUVA, surgery (lupus pernio) or intralesional chloroquine.



Specific investigations








First-line therapies
























image Topical corticosteroids C
image Intralesional corticosteroids C
image Oral corticosteroids C
image Chloroquine B
image Hydroxychloroquine C
image Methotrexate B








Evidence-based therapy for cutaneous sarcoidosis.

Baughman RP, Lower EE. Clin Dermatol 2007; 25: 334–40.


Whereas the recommended starting dose of prednisone for pulmonary sarcoidosis is suggested to be 20–40 mg daily, the dose and duration of treatment for cutaneous sarcoidosis has not been established. The authors suggest using this as a benchmark and tapering the steroid dose after 1 or 2 months to one that controls the disease while avoiding toxicity. The authors report that the need for long-term systemic corticosteroids for treatment of chronic sarcoidosis occurs in about a quarter of patients.


Another suggested regimen for prednisone in cutaneous sarcoidosis is 30 mg orally on alternate days until the granulomas fade. The dose is then tapered over several months to 15 mg orally on alternate days. Other protocols report a good response with prednisone 30–40 mg orally daily, with a gradual taper to 10–20 mg orally on alternate days for 1 year, or prednisone 1 mg/kg orally daily (maximum 60 mg) for 8 to 12 weeks, with a taper to 0.25 mg/kg daily continued for 6 months.


With long-term treatment, prevention of corticosteroid-induced osteoporosis with bisphosphonates and Pneumocystis pneumonia prophylaxis with trimethoprim–sulfamethoxazole should be considered.



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Aug 7, 2016 | Posted by in Dermatology | Comments Off on Sarcoidosis

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