After signing informed consent, the patient was hospitalized but surgery was not performed because the suspected parasite (likely Dirofilaria spp.) had migrated to the right parietal area of the head (i.e., the subcutaneous tissue at the parietal bone of the skull), preventing its removal. During her 5-day hospitalization, the patient was in good clinical condition; hematological and serologic biochemical parameters were within reference ranges; eosinophilia was not present. Infections by Strongyloides stercoralis and zoonotic filarial worms (i.e., Brugia spp., Wuchereria bancrofti, Mansonella spp., and Oncocherca spp.) were excluded by serologic assays (i.e., commercial ELISA kits). Chest radiography was performed to exclude the presence of coin lesions typical of Dirofilaria spp. infection.

We tested a serum sample at the Department of Public Health and Infectious Diseases Sapienza, University of Rome, to assess exposure to Dirofilaria spp. by using an in-house ELISA based on somatic antigens of adult D. repens (6,7), which yielded positive results (i.e., optical density 1.56; optical density cut off 1.03 for D. repens). The woman was discharged from the hospital with the recommendation to return on observation of parasite reemergence to the facial subcutaneous tissue.

Figure 1

Figure 1. Microscopic view of Dirofilaria repensnematode extracted from subcutaneous facial tissue of a patient, Italy. Microscopic analysis revealed a thick laminated cuticle with characteristic longitudinal ridges and cross-striations, leading...

Two weeks later, the nematode migrated in the frontal area, and a surgical excision was performed under local anesthesia. The specimen was shipped to the University of Bari (Italy) for further morphological and molecular analysis. The fragmented nematode was morphologically identified as a mature female, cylindrical, ≈2.96 cm in length, and 0.480 mm thick (Figure 1). Microscopic analysis revealed a thick laminated cuticle with characteristic longitudinal ridges and cross-striations (Figure 1), leading to the identification of the parasite as D. repens (8).

Figure 2

Figure 2. Phylogeny of Dirofilaria repens based on cox1 gene sequences in study of rapid subcutaneous migration of D. repensnematode in facial tissue, Italy. The sequence...

Genomic DNA was extracted from the nematode and tested by conventional PCR targeting cox1 gene (9) to obtain a reference sequence. BLAST (https://blast.ncbi.nlm.nih.gov) analysis revealed 100% nucleotide identity with reference sequence of D. repens in the GenBank database (accession no. MW675692), which further confirmed by phylogenetic analyses (Figure 2). At the 5-month follow-up, the patient’s only residual symptom was a persisting uncomfortable feeling, likely associated with parasite migration. We also performed specific tests to detect Dirofilaria spp. on her pets, yielding negative results.

The increasing incidence of human cases of dirofilariosis in Europe (10) underscores the need for including this emerging zoonotic disease in the differential diagnosis of pulmonary or subcutaneous nodules in absence of eosinophilia. The rapid migration of the nematode in this case was unusual, highlighting the variability of clinical signs in patients infected by D. repens nematodes, which range from stationary nodules to fast-migrating lesions in subcutaneous tissues. Human dirofilariosis is typically an abortive infection because humans are accidental hosts, and microfilaremia is absent (1). Consequently, traditional diagnostic methods applied in veterinary medicine (e.g., Knott’s test) are unsuitable. Definitive diagnosis in human patients is challenging, and often only achievable after surgical removal of the parasite.

In summary, we identified D. repens nematode infection in a woman with a creeping lesion in her subcutaneous facial tissue. This case highlights the need for a One Health approach in implementing vector control strategies and regular monitoring of reservoir hosts in endemic areas to mitigate the risk for human D. repens infection.