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Lofgren Syndrome in a 35-Year-Old Female: A Case Report
Abel Tenaw Tasamma1, Sebhatleab Teju Mulate1, Etsegenet Yayut Munie1
1School of Medicine College of Health Sciences, Addis Ababa University Addis Ababa Ethiopia.
Clinical Case Reports
|October 17, 2025
Summary
Lofgren syndrome, an acute sarcoidosis form, presents with fever, arthritis, and erythema nodosum. This case highlights a patient
Area of Science:
- Rheumatology
- Pulmonology
- Dermatology
Background:
- Lofgren syndrome is an acute presentation of sarcoidosis.
- It is characterized by fever, bilateral hilar lymphadenopathy, and erythema nodosum.
- Early diagnosis and treatment are crucial for patient outcomes.
Purpose of the Study:
- To present a case of Lofgren syndrome in a 35-year-old female patient from Ethiopia.
- To illustrate the diagnostic process and successful management of this condition.
- To emphasize the importance of recognizing Lofgren syndrome in clinical practice.
Main Methods:
- Case report of a patient presenting with arthritis, fever, and erythema nodosum.
- Diagnostic workup included chest imaging (X-ray and CT scan) to assess for lymphadenopathy and lung nodules.
- Exclusion of alternative diagnoses such as tuberculosis.
- Treatment initiated with low-dose prednisolone.
Main Results:
- The patient presented with acute arthritis, fever, and skin lesions consistent with erythema nodosum.
- Chest imaging confirmed bilateral hilar and mediastinal lymphadenopathy and perilymphatic nodules.
- Exclusionary workup ruled out tuberculosis.
- Low-dose prednisolone led to prompt symptom improvement.
Conclusions:
- Lofgren syndrome is a distinct clinical entity within sarcoidosis.
- Prompt diagnosis and corticosteroid treatment lead to favorable outcomes.
- This case underscores the importance of considering Lofgren syndrome in patients with compatible symptoms.
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