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[Pyoderma gangrenosum with aseptic spleen abscess]
N Brahimi1, E Maubec, O Boccara
1Service de dermatologie, hôpital Bichat, Assistance publique-Hôpitaux de Paris, université Paris-VII Denis-Diderot, 46, rue Henri-Huchard, 75877 Paris cedex 18, France.
Background:
Pyoderma gangrenosum is a neutrophilic dermatosis in which systemic involvement is rare. It may be associated with systemic disease. We report a case of pyoderma gangrenosum in the spleen.
Case Report:
A 68-year-old man presenting pyoderma gangrenosum with pustules and stage I multiple myeloma was admitted for asthenia and abdominal pain. There were no skin lesions. Laboratory tests showed inflammatory syndrome with polynuclear leucocytes of 25,000/mm(3). CAT scans and abdominal ultrasound revealed a splenic abscess. A spleen biopsy was performed and histological examination showed polynuclear leukocyte infiltration, while cultures were negatives. Diagnosis of pyoderma gangrenosum with splenic involvement was made. Increased systemic corticosteroid therapy produced a successful outcome. Haematological findings remained unchanged.
Discussion:
Spleen involvement in pyoderma gangrenosum is very rare and can mimic an infectious process. In such cases, routine screening is essential for associated diseases, particularly haematological malignancies.
Insights
Pyoderma gangrenosum rarely affects internal organs. This case highlights splenic involvement, mimicking infection, emphasizing the need for screening for associated hematologic malignancies.
Area of Science:
- Dermatology
- Internal Medicine
- Pathology
Background:
- Pyoderma gangrenosum (PG) is a neutrophilic dermatosis.
- Systemic involvement in PG is uncommon.
- PG can be associated with underlying systemic diseases.
Observation:
- A 68-year-old male with pustular PG and multiple myeloma presented with abdominal pain.
- Imaging revealed a splenic abscess.
- Histopathology showed leukocytic infiltration, with negative cultures.
Findings:
- The patient was diagnosed with splenic involvement of pyoderma gangrenosum.
- Treatment with systemic corticosteroids was successful.
- Hematological status remained stable.
Implications:
- Splenic involvement in PG is rare and can be misdiagnosed as infection.
- Routine screening for systemic diseases, especially hematologic malignancies, is crucial in PG cases.
- This case underscores the importance of a comprehensive diagnostic approach for pyoderma gangrenosum.
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