Challenging Mimickers in the Diagnosis of Sarcoidosis: A Case Study
Thomas El Jammal,
Yvan Jamilloux,
Mathieu Gerfaud-Valentin,
Gaëlle Richard-Colmant,
Emmanuelle Weber,
Arthur Bert,
Géraldine Androdias,
Pascal Sève
Affiliations
Thomas El Jammal
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Yvan Jamilloux
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Mathieu Gerfaud-Valentin
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Gaëlle Richard-Colmant
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Emmanuelle Weber
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Arthur Bert
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Géraldine Androdias
Department of Neurology, Service Sclérose en Plaques, Pathologies de la Myéline et Neuro-Inflammation, Hôpital Neurologique Pierre Wertheimer, Lyon University Hospital, F-69677 Bron, France
Pascal Sève
Department of Internal Medicine, Lyon University Hospital, 69004 Lyon, France
Sarcoidosis is a systemic granulomatous disease of unknown cause characterized by a wide variety of presentations. Its diagnosis is based on three major criteria: a clinical presentation compatible with sarcoidosis, the presence of non-necrotizing granulomatous inflammation in one or more tissue samples, and the exclusion of alternative causes of granulomatous disease. Many conditions may mimic a sarcoid-like granulomatous reaction. These conditions include infections, neoplasms, immunodeficiencies, and drug-induced diseases. Moreover, patients with sarcoidosis are at risk of developing opportunistic infections or lymphoma. Reliably confirming the diagnosis of sarcoidosis and better identifying new events are major clinical problems in daily practice. To address such issues, we present seven emblematic cases, seen in our department, over a ten-year period along with a literature review about case reports of conditions misdiagnosed as sarcoidosis.