InfectionCancer mimicICD-10 B42

Sporotrichosis

Rose-gardener's disease; sporotrichoid lymphocutaneous infection; Sporothrix schenckii infection

Sporotrichosis is a deep mycotic infection caused by the dimorphic fungus Sporothrix schenckii complex (including S. brasiliensis, S. globosa, S. luriei, S. mexicana). It is the prototypical cause of sporotrichoid lymphocutaneous spread — a primary inoculation nodule at the site of plant / soil trauma followed by a chain of subcutaneous nodules ascending along lymphatic drainage. Rose-gardener's disease is the classic exposure history. UK cases are sporadic, often in returning travellers from endemic areas (Latin America, southern Africa, South-East Asia). Itraconazole 100–200 mg daily for 3–6 months is the standard first-line therapy.

CurrentLast reviewed 15 May 2026

Clinical features

  • Primary inoculation nodule — small red-brown papule at site of plant / thorn / splinter trauma; develops 1–10 weeks after inoculation.
  • Lesion enlarges to a non-healing ulcer or violaceous nodule.
  • Sporotrichoid lymphocutaneous spread — secondary nodules at intervals along the lymphatic drainage of the affected limb, often appearing weeks after the primary.
  • Lymphadenopathy uncommon.
  • Constitutional symptoms uncommon in immunocompetent hosts.
  • Fixed cutaneous form — single non-spreading lesion (more common in endemic populations).
  • Extracutaneous and disseminated disease — pulmonary, osteoarticular, ocular, CNS — in immunosuppressed (HIV, transplant, alcohol).

Differential for sporotrichoid spread

  • Atypical mycobacterial infection (M. marinum, M. chelonae).
  • Nocardia brasiliensis.
  • Cutaneous leishmaniasis.
  • Cat-scratch disease (Bartonella).
  • Tularaemia.
  • Cutaneous tuberculosis (especially scrofuloderma).
  • Pyoderma gangrenosum (rare lymphocutaneous variant).
  • Inflammatory or hypersensitivity reactions.
  • Cancers — KA, cSCC (less likely to be multifocal).

Diagnosis

  • Detailed exposure history — gardening, sphagnum moss, rose handling, hay, returning traveller.
  • Skin biopsy with split tissue:
    • Histology — granulomatous inflammation, sometimes with characteristic asteroid bodies (rare). Cigar-shaped yeasts seen in tissue (variable yield).
    • Microbiology — fungal culture on Sabouraud agar at 25 °C and 37 °C (dimorphic — mould at 25, yeast at 37). Culture is the gold standard.
    • PCR — emerging where culture access limited.
  • Serological tests have limited utility.
  • Imaging — for osteoarticular extension if joint symptoms; CXR for pulmonary disease in immunosuppressed.

Management

  • First-line — itraconazole 100–200 mg daily for 3–6 months, continued until 1–2 months after clinical resolution.
  • Alternative — terbinafine 250–500 mg daily; potassium iodide solution (oldest treatment, less tolerable).
  • Disseminated / severe disease — amphotericin B (liposomal preferred) initially, transition to itraconazole maintenance.
  • Pregnancy — limited safe options; specialist input. Local heat therapy historically used.
  • Topical / intralesional therapy — limited role; surgical excision rarely indicated.
  • Follow-up — until at least one month after complete clinical resolution; recurrence rate ~ 5–10%.

References

  1. Kauffman CA et al. Clinical practice guidelines for the management of sporotrichosis — IDSA. Clin Infect Dis; 2007.
  2. Chakrabarti A et al. Global epidemiology of sporotrichosis. Med Mycol; 2015.

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