Primary cutaneous plasmacytosis

Get in touch with RARE Concierge.

Contact RARE Concierge

Primary cutaneous plasmacytosis

A rare acquired skin disease characterized by benign proliferation of mature plasma cells with a typical triad of cutaneous lesions polyclonal hypergammaglobulinemia and superficial lymphadenopathy without an apparent underlying cause. The skin lesions consist of multiple round-to-oval red-to-dark-brown macules papules and plaques most commonly found on the trunk but also the face neck and axillae.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: // Data version October 2023.

Newly diagnosed with
Primary cutaneous plasmacytosis?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Clinical Trials

For a list of clinical trials in this disease area, please click here.