Author: Dr Ben Tallon, Dermatologist/Dermatopathologist, Tauranga, New Zealand, 2011.
Histology of Wells syndrome
Scanning power view of Wells syndrome reveals a superficial and deep perivascular and interstitialinflammatory pattern (Figures 1 and 2). This can be seen to extend into the subcutaneous tissue (Figure 3) or even the underlying muscle. The inflammatoryinfiltrate is comprised of lymphocytes, histiocytes and abundant eosinophils (Figures 4,5 and 6). Degranulation of the eosinophils is seen forming flame figures (Figures 4 and 5). In this particular case extensive interstitial mucin is seen (Figures 4 and 5).
Bullous Wells disease: A subepidermal blister can form in the presence of prominent papillary dermaloedema.
Differential diagnosis of Wells syndromepathology
Insect bite reaction: Typically here the infiltrate is more localised forming a wedge shaped pattern possibly with focal overlying epidermal changes. In some cases discrimination is not possible and clinical correlation is required.
Bullous pemphigoid: In most circumstances it is the urticarial phase of bullous pemphigoid which may prove difficult to discriminate. Eosinophils can be seen to tag along the dermoepidermal junction in conjunction with basal layervacuolar degeneration
Churg Strauss syndrome: While dermaleosinophilia and flame figures can be seen, this condition is characterised by necrotising granuloma formation and variable degrees of vasculitis.
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