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CD30-Positive Angioinvasive Lymphomatoid Papulosis (Type E) Developing from Parapsoriasis en Plaque
Taku Fujimura1, Chunbing Lyu1, Kenichiro Tsuchiyama1
1Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Case Reports in Oncology
|January 29, 2019
Summary
This report details a rare case of angioinvasive lymphomatoid papulosis (LyP) type E originating from parapsoriasis en plaque. It highlights the unique development pathway of this CD30+ CD8+ lymphocyte-infiltrated skin condition.
Area of Science:
- Dermatopathology
- Oncodermatology
Background:
- Lymphomatoid papulosis (LyP) is a rare primary cutaneous CD30-positive lymphoproliferative disorder.
- Type E LyP is characterized by angioinvasion and angiodestruction, with CD30+ and CD8+ lymphocyte infiltration.
- While LyP can co-occur with mycosis fungoides, LyP type E developing from parapsoriasis en plaque is not previously reported in English literature.
Observation:
- A case of angioinvasive LyP (type E) developing from parapsoriasis en plaque was observed.
- The patient's condition exhibited characteristic angiocentric and angiodestructive features.
- Immunohistochemical staining was utilized to investigate the underlying pathomechanisms.
Findings:
- The study describes the first reported instance of LyP type E arising from parapsoriasis en plaque.
- Immunohistochemical analysis provided insights into the pathomechanisms of this rare presentation.
- The findings contribute to understanding the spectrum of LyP and its potential evolution.
Implications:
- This case expands the known clinical spectrum of lymphomatoid papulosis.
- It underscores the importance of considering LyP type E in cases of parapsoriasis en plaque with concerning features.
- Further research into the pathogenesis of LyP evolving from precursor lesions is warranted.
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