Jul 2026· Vestnik Dermatologii i Venerologii· Vol 102, pp. 61-68· 0 citations· 8 references
TL;DR
A case of cutaneous protothecosis is reported in a 78-year-old woman with a long history of pruritic skin eruptions and a history of uncontrolled long-term use of topical corticosteroids, confirming the diagnosis of protothecosis.
Abstract
Cutaneous protothecosis is a rare opportunistic infection caused by achlorophyllous algae of the genus Prototheca and often poses a diagnostic challenge because of marked clinical polymorphism and the absence of pathognomonic features. We report a case of cutaneous protothecosis in a 78-year-old woman with a long history of pruritic skin eruptions and a history of uncontrolled long-term use of topical corticosteroids. During prior evaluation, systemic connective tissue disease and a paraneoplastic etiology of the cutaneous process were excluded. The key diagnostic step was a skin biopsy with histopathological examination, which demonstrated a lichenoid pattern combined with productive granulomatous inflammation in the dermis, raising suspicion of an infectious dermatosis and prompting additional special stains. Ziehl–Neelsen staining was negative, excluding mycobacterial infection. Periodic acid–Schiff (PAS) staining revealed PAS-positive structures. Culture of shave-biopsy material on Sabouraud dextrose agar yielded Prototheca wickerhamii, confirming the diagnosis of protothecosis. The patient was started on itraconazole 100 mg twice daily, with gradual regression of skin lesions and improvement of subjective symptoms.
This case shows that persistent skin lesions in immunosuppressed patients warrant broad investigation, even during antifungal treatment, and that protothecosis should be considered in this differential diagnosis of histoplasmosis and cutaneous protothecosis in patients on anti-TNF-alpha therapy.
Luana Araujo Brezolin, A. Bertucci, Fernanda Cristina Galerani Gualtieri Parpinelli et al.· ARACÊ· 0 citations
A 77-year-old woman with a medical history of hypertension and diabetes presented with ulcerated purplish-red nodules on the lower extremities that had persisted for 3 months, and subsequent treatment with oral trimethoprim–sulfamethoxazole led to gradual regression of the lesions and scar formation.
Nai-Xuan Lin, Ke-Ke Huang, De-Gang Yang· American Journal of Tropical...· 0 citations
A 67-year-old woman who presented with progressive skin erythema and pustules for two months, unresponsive to topical halometasone is reported, demonstrating that primary cutaneous infections can occur in non-transplant hosts.
Chun-Li Yang, Zheng Lin, Dong-Ping Yang et al.· Frontiers in Medicine· 0 citations
ABSTRACT
Majocchi's granuloma is a deep folliculocentric fungal infection characterized by suppurative and granulomatous inflammation, most commonly caused by dermatophytes. Non-dermatophytic molds, including Aspergillus species, are uncommon etiological agents. We report a 20-year-old immunocompetent male presenting w...
Ashish Jagati, Hetal Vaghela, J. Buch et al.· American journal of dermatop...· 0 citations
Disseminated histoplasmosis is an opportunistic fungal infection caused by
Histoplasma capsulatum
that commonly affects immunocompromised individuals. Cutaneous manifestations are polymorphic and may mimic several dermatological disorders, leading to diagnostic difficulty. We report a 33-year-old renal transplant r...
Kartik Saini, Sushantika Sushantika, Prashant Durgapal et al.· Journal of Skin and Sexually...· 0 citations
Phaeohyphomycoses are rare infections caused by melanin-pigmented, saprophytic fungi commonly found in soil and on decaying plant matter. Infections typically affect immunocompromised individuals and present a wide clinical spectrum. Here, we report the case of a 63-year-old immunocompromised patient, with a history of...
Rihab Trabelsi, M. Zlobecki, M. Moniot et al.· Mycopathologia· 0 citations
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