Clinicopathologic Features and Pre-diagnostic Spectrum of Nail Unit Squamous Cell Carcinoma: A 10-Patient Case Series


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Aygün Alızada M., Heper A., Kırmızı B. A., Koçyiğit P.

EADV SYMPOSIUM 2026, ATHENS, Athens, Yunanistan, 7 - 09 Mayıs 2026, ss.197-198, (Özet Bildiri)

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Athens
  • Basıldığı Ülke: Yunanistan
  • Sayfa Sayıları: ss.197-198
  • Ankara Üniversitesi Adresli: Evet

Özet

Nail unit squamous cell carcinoma (nSCC), including nSCC in situ (Bowen disease), is the most common malignant tumor of the nail unit and presents with a broad and often misleading clinical spectrum. Because these lesions frequently mimic infections or benign subungual solitary and pigmentary conditions, diagnosis is commonly delayed for years (1–4). Early recognition requires a high index of suspicion, awareness of warning clinical features, and timely nail unit biopsy using an appropriate technique followed by careful dermatopathological evaluation. The aim of this study was to evaluate the clinical and epidemiological characteristics of patients with subungual squamous cell carcinoma, focusing on clinical presentation, diagnostic challenges, diagnostic work-up, and treatment outcomes. A retrospective evaluation was conducted on 10 patients with histopathologically confirmed nSCC or nSCC in situ diagnosed between 2022 and 2025. Epidemiologic characteristics and risk factors, clinical features, clinical prediagnoses, final dermatopathological diagnosis (in situ or invasive), HPV status (when molecular testing was available), and planned treatment modalities were analyzed. A total of 10 patients were included (6 males, 4 females), with a mean age of 59.5 ± 14.7 years (24–79 years). Lesions were located on the hand in 60% (6/10) and on the foot in 40% (4/10), with predominant involvement of the first digit/thumb in 70% (7/10). The most common presenting findings were subungual hyperkeratosis (50%, 5/10) and discharge (50%, 5/10), followed by ulceration (30%, 3/10), nail color changes (30%, 3/10), nail dystrophy (30%, 3/10), and subungual mass formation (30%, 3/10) (Table 1). Verrucous lesions were observed in 20% (2/10). A history of trauma was present in one patient. The mean interval between lesion onset and definitive diagnosis was 30.5 months (4–96 months). Six patients had previously received treatment for presumed onychomycosis, and three had undergone prior nail avulsion. Histopathologically, 20% of cases were classified as nSCC in situ and 80% as invasive nSCC. High-risk HPV was detected in 33.3% (2/6) of tested patients. Therapeutic wide local excision was performed in 60%, while bone invasion– associated amputation was performed in 30%. nSCC predominantly affects individuals over 50 years of age, shows male predominance, and most frequently involves the first digit (1,2). Consistent with the literature, the mean age in our cohort was 59.5 years, 60% of patients were male, and first-digit involvement was observed in 70%. All cases presented with single-nail involvement, and the most common findings were subungual hyperkeratosis (%50), discharge (%50), and nail dystrophy (%30), reflecting the nonspecific clinical presentation of nSCC (1,3). Nonspecific features contribute to diagnostic delays of up to 5–7 years in previous reports (1,3); in our cohort, the mean delay was 30.5 months. While amputation rates of approximately 20% have been reported (2), amputation was required in 30% of our patients, emphasizing the importance of early diagnosis to prevent advanced disease and limb-sacrificing surgery. Although high-risk HPV has been reported in 60–80% of cases (4), positivity was detected in only 30% of our series, indicating that nSCC is not exclusively HPV-related. The primary therapeutic goal is complete tumor excision with histologically clear margins; accordingly, wide local excision with margins exceeding 4–6 mm was performed in 60% of patients, in line with current recommendations (2,5).