Pyoderma gangrenosum of the hand: a missed diagnosis and lessons learned

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Abstract

INTRODUCTION: Pyoderma gangrenosum (PG) is a challenging condition to diagnose and treat.

CASE REPORT: We discuss the case of a man who presented with a swollen and extremely tender finger, with bullous lesions, erythema, and a clinical picture suggestive of a necrotising fasciitis. He had a history of ulcerative colitis (UC) and had been taking azathioprine. Initial debridement of the affected tissues was carried out as an emergency, with no improvement. Pyoderma gangrenosum had been suspected at that stage and the patient was prescribed oral Prednisolone. He showed a remarkable recovery and his finger healed completely. Due to a persistent pancytopenia he underwent further tests and was subsequently diagnosed with Acute myeloid leukaemia (AML).

DISCUSSSION: Pyoderma gangrenosum is a diagnosis of exclusion. It can be a sign of internal malignancy and other medical conditions. Therefore, a low threshold must be kept for the diagnosis of this disorder, especially in patients with known risk factors.

CONCLUSION: Based on our experience, in similar clinical scenarios, we suggest limb elevation and antibiotics initially, with a close observation and consideration of the diagnosis of pyoderma gangrenosum prior to any surgical intervention. A thorough investigation of the possible reasons for PG is vitally important.

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About the authors

K. Maheshwari

Bedfordshire Hospitals NHS Foundation Trust

Email: snarskaya-dok@mail.ru
United Kingdom, Bedfordshire

A. Yousif

Bedfordshire Hospitals NHS Foundation Trust

Email: snarskaya-dok@mail.ru
Russian Federation, Bedfordshire

E. Burova

Bedfordshire Hospitals NHS Foundation Trust

Author for correspondence.
Email: snarskaya-dok@mail.ru

Consultant Dermatologist

United Kingdom, Bedfordshire

References

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Supplementary files

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2. Figure 1. Finger at presentation to the accident and emrgency department.

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3. Figure 2. Three days later. a – palmar aspect; b – dorsal aspect; at this point the decision was made to proceed with surgical debridement.

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4. Figure 3. Two weeks after starting oral steroids.

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5. Figure 4. Four weeks after starting steroids (a); b – four weeks after commencing steroids, dorsal aspect. The patient showed remarkable re-epithelisation wihout the need for any surgical intervention.

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