Post-Traumatic Primary Cutaneous Cryptococcosis Presenting as a Chronic Refractory Forearm Ulcer with Polymicrobial Coinfection: An mNGS-Assisted Case Report and Literature Review
Sep 2026· Clinical, Cosmetic and Investigational Dermatology· Vol 19, pp. 1-7· 0 citations· 12 references
Medicine
TL;DR
PCC should be considered in chronic post-traumatic ulcers, with systematic evaluation for extracutaneous involvement before establishing a primary cutaneous diagnosis, according to a 52-year-old male farmer with type 2 diabetes who developed chronic refractory ulcers on the right forearm following suspected insect-bite trauma.
Abstract
Abstract Primary cutaneous cryptococcosis (PCC) is a rare infection caused by direct inoculation of Cryptococcus through disrupted skin. We report a 52-year-old male farmer with type 2 diabetes but no HIV infection or known major immunosuppressive disease who developed chronic refractory ulcers on the right forearm following suspected insect-bite trauma. Cryptococcus neoformans was isolated from cutaneous specimens. Probe-capture metagenomic next-generation sequencing (MetaCAP) of the ulcer tissue additionally detected C. neoformans at 202 reads per million (RPM), accounting for 91.98% of the fungal sequences, with a reported confidence of 99%. Histopathology demonstrated an infectious granuloma, while bacterial culture identified methicillin-resistant Staphylococcus aureus and extended-spectrum β-lactamase-producing Escherichia coli. Chest computed tomography and cerebrospinal fluid investigations did not support pulmonary or central nervous system cryptococcosis. Liposomal amphotericin B was discontinued because of acute kidney injury, and subsequent fluconazole plus flucytosine treatment resulted in reduced exudation, granulation tissue formation, and partial ulcer healing. PCC should be considered in chronic post-traumatic ulcers, with systematic evaluation for extracutaneous involvement before establishing a primary cutaneous diagnosis.
Cryptococcus neoformans typically causes pulmonary or central nervous system (CNS) infections. However, osteoarticular manifestations, particularly as the initial presentation, are rare, especially in immunocompetent hosts. We report the case of a 65-year-old apparently immunocompetent woman admitted for generalized pa...
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Chun-Mei Zhang, Jie Zhu, Juan Luo et al.· Infection and Drug Resistanc...· 0 citations
Melioidosis, caused by Burkholderia pseudomallei, produces a wide range of clinical manifestations and may be difficult to diagnose in the pediatric population. We describe the case of a 12-year-old girl with poorly controlled type 1 diabetes mellitus that posed diagnostic challenges. Over 4 months, she experienced rel...
Nikhil John, Pediredla Karunakar, Rajashree Choudhury et al.· Paediatrics and Internationa...· 0 citations
Clinicians should maintain a high index of suspicion for mucormycosis in diabetic patients presenting with rapidly progressive necrotic soft tissue infections despite negative initial fungal microscopy or the isolation of bacterial pathogens.
Y. Hartantri, Stephanie Victoria Gunadi, Ferdy Ferdian et al.· International Medical Case R...· 0 citations
Among published cases, cutaneous cryptococcosis most commonly occurred in the setting of disseminated infection, and a high index of suspicion and prompt diagnostic evaluation are essential to ensure early recognition and improve clinical outcomes.
V. Scaglione, Simone Melchiorri, Marco Cola et al.· International Journal of Inf...· 0 citations
Mucormycosis is an aggressive angioinvasive fungal infection that predominantly affects chronically immunosuppressed individuals. Hematogenous dissemination of
Mucorales
causing synchronous gastric full-thickness perforation and total splenic infarction is exceptionally rare, particularly in immunocompetent hos...