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Pityriasis lichenoides et varioliformis acuta pathology

Authors: Dr Achala Liyanage, Dermatology Fellow, Waikato Hospital, Hamilton, New Zealand; Assoc Prof Patrick Emanuel, Dermatopathologist, Auckland, New Zealand. January 2015.

Pityriasis lichenoides et varioliformis acuta pathology — codes and concepts

Pityriasis lichenoides et varioliformis acuta (PLEVA) presents with haemorrhagic papules that resolve to leave varioliform scars. It is usually a self-limiting acute dermatosis. It is also known as Mucha Habermann disease.

Histology of PLEVA

PLEVA has sharply delimited, moderately dense, lymphocytic infiltrate involving the superficial vascular plexus, which extends in a wedge-shaped pattern to involve the lower dermis (figure 1). The superficial dermis shows a dense lichenoid infiltrate and impressive exocytosis of lymphocytes into the epidermis. The overlying stratum corneum shows parakeratosis which may be confluent and contain collections of neutrophils (figure 2). The epidermis shows pronounced hydropic change and foci of keratinocyte necrosis. Scattered extravasated erythrocytes are seen (figure 3).

Pityriasis lichenoides et varioliformis acuta (PLEVA) pathology

Images provided by Dr Duncan Lamont, Waikato Hospital

Special studies in PLEVA

None are generally needed. Immunoperoxidase studies have shown the lymphocytic infiltrate consists of CD8/cytotoxic T cells.

Differential diagnosis of PLEVA

Cutaneous T-cell lymphoma

Lymphocytic vasculitis

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Related information



  • Weedon’s Skin Pathology (Third edition, 2010). David Weedon

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