02125nas a2200229 4500000000100000008004100001260005300042653002200095653003400117653002600151653001700177653003100194653002400225100001600249700000800265245011700273856008800390300001000478490000700488520138600495022001401881 2026 d c06/2026bSpringer Science and Business Media LLC10a ace serum levels10aChronic granulomatous disease10aCutaneous Sarcoidosis10askin nodules10atuberculosis masquerading 10alepromatous leprosy1 aPrashanth G1 aT D00aLepromatous Leprosy Mimicking Sarcoidosis With Elevated Serum ACE Levels: A Deceptive Granulomatous Presentation uhttps://assets.cureus.com/uploads/case_report/pdf/489738/20260506-118706-shmtrj.pdf a1 - 70 v183 a
diagnostic challenge, particularly in regions endemic for tuberculosis. We report the case of a 68-year-old diabetic male with a significant smoking history who presented with progressive shortness of breath and cough for almost three weeks' duration and multiple cutaneous nodules, present for six years, that increased in size and number over two months before presentation. Initial evaluation revealed normal chest imaging, negative microbiological tests for tuberculosis, a non-reactive Mantoux test, and elevated serum angiotensin-converting enzyme (ACE) levels, raising suspicion for the presence of granulomatous disease, like cutaneous tuberculosis, sarcoidosis, and other non-tuberculosis mycobacteria. However, further evaluation, including dermatological assessment and histopathological examination of skin lesions, which demonstrated foamy histiocytic infiltration, was performed. Wade-Fite staining revealed numerous acid-fast bacilli with a high bacterial index, confirming the diagnosis of lepromatous leprosy. The patient was initiated on multidrug therapy with rifampicin, dapsone, and clofazimine, with close follow-up. This case highlights the importance of maintaining a broad differential diagnosis in granulomatous diseases and emphasizes the need for tissue diagnosis before initiating empirical therapy, especially in tuberculosisendemic settings.
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