Are dissecting cellulitis and hidradenitis suppurativa different diseases?

Alessandro Federico1, Alfredo Rossi1, Gemma Caro1

  • 1Dermatology Unit, Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.

Clinics in Dermatology
|September 14, 2021
PubMed

Insights

Dissecting cellulitis (DC) and hidradenitis suppurativa (HS) share many features, suggesting they may be different manifestations of the same follicular occlusion disease. This perspective could refine understanding and treatment of these scalp and body conditions.

Area of Science:

  • Dermatology
  • Pathogenesis of skin conditions

Background:

  • Dissecting cellulitis (DC) and hidradenitis suppurativa (HS) are distinct diagnoses with overlapping clinical, pathogenetic, and therapeutic features.
  • Both conditions are associated with acne conglobata, forming the follicular occlusion triad or tetrad.
  • DC involves perifolliculitis, abscesses, sinus tracts, and scarring alopecia on the scalp.
  • HS is a chronic inflammatory disease of apocrine gland-rich areas, characterized by nodules, abscesses, sinus tracts, and scarring.

Purpose of the Study:

  • To evaluate the overlapping features of dissecting cellulitis and hidradenitis suppurativa.
  • To propose a unified classification for these related conditions.

Main Methods:

  • Comparative analysis of clinical, dermatoscopic, pathogenetic, and histologic aspects of DC and HS.
  • Review of existing literature on follicular occlusion disorders.

Main Results:

  • Significant overlap exists between DC and HS in terms of clinical presentation, pathogenesis, and treatment modalities.
  • The conditions share features such as perifolliculitis, abscess formation, sinus tracts, and scarring.
  • Both are classified as neutrophilic, cicatricial alopecias or chronic inflammatory diseases.

Conclusions:

  • DC and HS exhibit substantial similarities, supporting the hypothesis that they represent different localizations of a single disease process.
  • Reclassifying DC and HS as variants of a follicular occlusion disease could improve diagnostic and therapeutic approaches.
  • This unified perspective highlights the follicular occlusion disease occurring on the scalp (DC) and apocrine gland-rich areas (HS).

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