• Case Report
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  • Open Access

Subungual bowen disease simulating onychopapilloma: Case report

  • Aicha Elharrouni Alaoui;
    • Departement of dermatology, CHU Hassan II, FES, Morocco
  • Issoual Khadija;
    • Departement of dermatology, CHU Hassan II, FES, Morocco
  • Gellouj Salim;
    • Departement of dermatology, CHU Hassan II, FES, Morocco
  • Fz Mernissi
    • Departement of dermatology, CHU Hassan II, FES, Morocco
  • Corresponding Author(s): : Aicha Elharrouni Alaoui

  • Departement of dermatology, CHU Hassan II, FES, Morocco

  • : ealaouiaicha@gmail.com

  • Elharrouni Alaoui A (2019).

  • This Article is distributed under the terms of Creative Commons Attribution 4.0 International License

Received : Sep 12, 2019
Accepted : Dec 10, 2019
Published Online : Dec 13, 2019
Journal : Journal of Case Reports and Medical Images
Publisher : MedDocs Publishers LLC
Online edition : http://meddocsonline.org

Cite this article: Elharrouni Alaoui A, Issoual Kh, Gellouj S , Mernissi Fz. Subungual bowen disease simulating onychopapilloma: Case report. J Case Rep Clin Images. 2019; 2(1): 1029.

Abstract

Most cases of Localized Longitudinal Erythronychia (LLE) represent local processes, in particular neoplastic, pressurerelated, or scar, whereas Polydactylous Longitudinal Erythronychia (PLE) cases are usually caused by inflammatory or acantholytic processes, or simply idiopathic. Bowen disease is the most frequent nail malignancy, usually seen as a verrucous lesion of the nail but it can be revealed by longitudinal erythronychia. Herein, we report a case of 38-year-old female who presented with a longitudinal erythronychia band on the 3rd left nail. Clinically differential diagnosis was an onychopapilloma. Surgical excision was performed. Histopathological examination, and Immunohistochemistry confirmed the diagnosis of Subungual Bowen disease.

Keywords: Bowen disease; Nail; Longitudinal erythronychia

Introduction

      Squamous cell carcinoma is a common carcinoma of the nail, but Bowen’s disease - SCC in situ is rarely diagnosed. Longitudinal Erythronychy (LE) is one of the most underestimated clinical presentations [1,2]. There are several differential diagnoses including other neoplasias, scars, inflammatory and infectious origins. It is therefore always useful in many cases to make a clinico-pathological correlation to retain the diagnosis. Malignancy is uncommon, but not rare, squamous cell carcinoma in situ is the most common malignancy. We report a case of subungual Bowen disease revealed by longitudinal erythronchia in a 38-year-old woman.

Case Report

      We report a case of a 38-year-old woman with no significant medical history, presented to our departement of dermatology with a 4-years history of a 2-mm-wide longitudinal erythronychia band on the 3rd left nail of the dominant hand with no history of infection, trauma or radiation. Clinical examination revealed the presence of a longitudinal erythematous band with distal encoched onycholysis. Dermoscopy showed longitudinal erythronychia followed by leukonychia and at the free edge of the nail: Subungual keratosis in the junction area between the nail plate and the band. After avulsion of the nail plate, a longitudinal excision biopsy of the nail unit including the distal matrix, the nail bed and the hyponychium was then performed. Anathomopathology showed a proliferation of keratinocytes that were atypical and non-aligned in the epidermis of the proximal and nail matrix beds, with normal aligned keratinocytes in the distal side. We retained the diagnosis of subungual bowen disease and additional excision was performed accordingly. Five months later, there was no evidence of recurrence.

Discussion

      Subungual Bowen disease remains uncommon, often diagnosed late. The age of onset is between 50 to 70 years old with a male predominance and it sits most often at the nails of the first three fingers of the left hand [4,5]. The duration of evolution of lesions at presentation varies between 3 to 5 years.

      At the beginning the lesion sits at the lateral nailfold with a progressive extension towards the nail bed and the matrix. Distal onycholysis may occur and is related to the presence of abnormal keratin in the nail bed which may also cause nail dystrophy or detachment of the nail plate. Dermatoscopy of subungual bowen disease is not clearly described in the literature; In our case, it appears to be the primary differential diagnosis of a benign tumor called onychopapilloma [6,7]. This diagnosis is confirmed by histopathological examination. The treatment of choice is based on the total surgical excision of the tumor for curative and conservative purposes taking into account the aesthetic concern. This attitude implies a good comprehension of the anatomy of the nail apparatus in view of the technical difficulties that can be encountered [5]. Mohs surgery for nail tumors is well established and increasingly used [5].

Conclusion

      Not every longitudinal erythronychia with subungueal hyperkeratosis should be considered onychopapilloma ; but practicians should be aware and perform a histopathological diagnosis to confirm the diagnosis.

Figure 1: Subungual Bowen disease. A: Clinical image of Longitudinal erythronychia. B: Dermatoscopic image of nail plate. C: Five months after surgery

References

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  2. Baran R, Simon C. Longitudinal melanonychia: a symptom of Bowen’s disease. J Am Acad Dermatol 1988; 18: 1359-1360.
  3. Lecerf P, Richert B, Theunis A, Andr_eJ. A retrospective study of squamous cell carcinoma of the nail unit diagnosed in a Belgian general hospitalover a 15-year period. J Am Acad Dermatol 2013; 69: 253-261.
  4. Goldminz D, Bennett RG. Mohs micrographic surgery of the nail unit. J Dermatol Surg Oncol 1992; 18: 721-726.
  5. Haneke E. Malignant nail tumors. Hautarzt. 2014; 65: 312-320.
  6. Saito T, Uchi H, Moroi Y, Kiryu H, Furue M. Subungual Bowen disease revealed by longitudinal melanonychia. J Am Acad Dermatol. 2012; 67: 240-241.
  7. Haneke E. Epidermoid carcinoma (Bowen’s disease) of the nail simulating acquired ungual fibrokeratoma. Skin Cancer. 1991; 6: 217-221.

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