Thursday, 29 December 2016

Cutaneous B-cell lymphoma (CBCL)


What is cutaneous B-cell lymphoma (CBCL)?


  • It can be either primary disease of the skin or secondary from nodal (non-Hodgkin's) lymphoma
  • It is rare and less common than mycosis fungicides
  • Men are more commonly affected, most cases present in the sixth or seventh decade of life


How does it present?
  • solitary or multiple nodules localised to one area of the body
  • Usually pink or violaceous in colour, smooth, firm, non tender 
  • favour neck and head region
  • lymph nodes in other area may be involved 

What does it look like on skin biopsy?

  • dense infiltrate of lymphocytes throughout the mid and lower dermis 
  • B lymphocytes do not localise to the epidermis, hence, no scale
What is the treatment ? 
  • Referral to a dermatologist or oncologist is recommended for staging and treatment 
  • Treatment options 
    • radiotherapy 
    • surgery for localised lesion s
    • chemotherapy 
    • rituximab 
What is the prognosis?
  • In general good prognosis > 90 % 5 year survival rate for the follicle centre and marginal zone b cell lymphoma 
  • less so for the variant occurring on the legs 
  • Secondary CBCL is associated with a poor prognosis 
Reference:
1. primary certificate of dermatology RACGP 

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