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Pityriasis Lichenoides-Like Mycosis Fungoides: A Case Report
Lily Park1, Claudia Green2, Derrek M Giansiracusa2
1Dermatology, Larkin Community Hospital, Miami, USA.
Cureus
|April 28, 2023
Summary
Pityriasis lichenoides-like mycosis fungoides (PL-like MF) is a rare subtype of mycosis fungoides. Recognizing this indolent CD8+ cutaneous T-cell lymphoma variant aids appropriate patient counseling.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Mycosis fungoides (MF) is the most common type of cutaneous T-cell lymphoma (CTCL).
- Pityriasis lichenoides-like mycosis fungoides (PL-like MF) is a rare subtype characterized by specific clinical and histological features.
- CD8+ CTCL encompasses both aggressive and indolent variants, necessitating accurate diagnosis for prognostic assessment.
Observation:
- A 64-year-old male presented with recurrent psoriasiform papules and mild scaling on the trunk and extremities.
- Clinical presentation mimicked pityriasis lichenoides (PL).
- Skin biopsy revealed histological findings consistent with CD8+ cutaneous T-cell lymphoma (CTCL).
Findings:
- The patient's presentation combined clinical features of pityriasis lichenoides with histological evidence of CD8+ mycosis fungoides.
- Differential diagnoses included pityriasis lichenoides, lymphomatoid papulosis, and PL-like MF.
- The case highlights a rare, indolent variant of CD8+ CTCL.
Implications:
- Accurate identification of PL-like MF is crucial for differentiating it from more aggressive CD8+ CTCL subtypes.
- Distinguishing indolent from aggressive variants allows for appropriate patient counseling regarding prognosis and management.
- This recognition aids clinicians in providing tailored care for patients with CD8+ cutaneous T-cell lymphoma.
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