Majochhi’s granuloma (MG) is a rare subtype of tinea infection characterized by a deep granulomatous inflammation. In most cases, it occurs in the presence of pre-existing chronic dermatophytoses, such as tinea corporis and tinea unguium. A combination of systemic and topical antifungals is necessary for the complete resolution of lesions.
In this article, we offer deep insights into the current perspectives on MG in relevance to its clinical features, predisposing factors, laboratory diagnosis, and treatment strategies.