eMedicine Specialties > Dermatology > Reactive & Inflammatory Dermatoses
Sarcoidosis: Follow-up
Updated: Sep 8, 2009
Follow-up
Further Inpatient Care
- Inpatient care is rarely needed for patients with cutaneous disease. However, in patients with respiratory insufficiency, hospitalization may be needed. Also, some patients may develop infections while on corticosteroids and/or immunosuppressive therapy that may result in hospitalization.
Further Outpatient Care
- Follow-up care should be frequent for the first 2 years after diagnosis.
- Patients with stage I disease can receive follow-up care twice yearly, whereas patients with more advanced lung disease should be seen more frequently. All patients should be monitored for at least 3 years after discontinuation of therapy.
- During follow-up care, patients should have a history with review of systems, physical examination, chest radiography, and pulmonary function tests to evaluate for active or insidiously progressive disease.
- Ophthalmologic assessment is needed initially—generally annually in all patients, and more frequently in those with ocular involvement. Therapeutic use of hydroxychloroquine (Plaquenil) may also warrant more frequent, detailed ophthalmologic examinations.
- A large review by Ji et al of the Swedish Hospital Registry noted an elevated risk of skin cancer (especially squamous cell carcinoma), non-Hodgkin lymphoma, and leukemia in hospitalized patients with sarcoidosis, extending beyond the first year after hospitalization. Therefore, close follow up for malignancies is recommended.35
Prognosis
- The course of the disease is variable, but spontaneous remission occurs in 50% of patients, while another one third of patients have eventual improvement. About 10-30% of patients have chronic or progressive disease.
- The mortality rate is 1-6%. In the United States, mortality is most commonly due to respiratory failure from pulmonary involvement, cardiac involvement, or neurosarcoidosis. Complications of therapy are additional causes of morbidity and mortality.
- Adverse prognostic factors include African American race, chronic cutaneous lesions, chronic uveitis, age at onset older than 40 years, cystic bone lesions, neurosarcoidosis, myocardial involvement, and stage III or IV pulmonary disease.
Miscellaneous
Medicolegal Pitfalls
- Misdiagnosis
- Toxicity from therapy, especially in an uninformed or unreliable patient
- Failure to recognize systemic or ocular involvement
More on Sarcoidosis |
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| Differential Diagnoses & Workup: Sarcoidosis |
| Treatment & Medication: Sarcoidosis |
Follow-up: Sarcoidosis |
| Multimedia: Sarcoidosis |
| References |
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Further Reading
Keywords
sarcoidosis, angiolupoid sarcoid, Besnier-Boeck-Schaumann disease, Boeck's sarcoid, Darier-Roussy disease, lupus pernio, multiple benign sarcoid of Boeck, Schaumann benign lymphogranulomatosis, subcutaneous sarcoid, uveoparotid fever
Follow-up: Sarcoidosis