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Necrotizing Granulomatous Dermatitis and Panniculitis Masquerading as T Cell Lymphoma
Daniel J Lewis1,2, Benjamin A Falck3, Sara M Kantrow4
1School of Medicine, Baylor College of Medicine, Houston, TX.
Skinmed
|January 7, 2020
Summary
A patient with ulcerative colitis presented with painful skin nodules that did not respond to antibiotics. Further molecular testing revealed T cell receptor gene rearrangements, suggesting a rare T cell lymphoma.
Area of Science:
- Dermatology
- Oncology
- Rheumatology
Background:
- A 51-year-old woman with a history of steroid-dependent ulcerative colitis, rheumatoid arthritis, and diabetes mellitus presented with concerning skin lesions.
- The patient developed painful, erythematous subcutaneous nodules on her thighs, accompanied by fever.
Observation:
- Initial histopathology suggested an abscess, but the lesions did not improve with broad-spectrum antibiotics.
- The nodules progressed to exhibit signs of necrosis, necessitating surgical debridement and hyperbaric oxygen therapy.
Findings:
- Molecular studies detected T cell receptor-beta (TCR-β) gene rearrangements.
- These findings, coupled with the clinical presentation and resistance to antibiotics, raised suspicion for a neoplastic process.
Implications:
- The patient was referred for further evaluation of possible subcutaneous panniculitis-like T cell lymphoma (SPTL).
- This case highlights the importance of considering rare hematologic malignancies in the differential diagnosis of refractory skin lesions.
- Early recognition and appropriate molecular diagnostics are crucial for managing SPTL.
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