Benign mimic · Connective tissueICD-10 L91.8

Acrochordon (skin tag)

Skin tag; fibroepithelial polyp; "tag"; soft fibroma; "Birt-Hogg-Dubé acrochordon" (when in syndromic context)

The acrochordon — universally known as a "skin tag" — is a small, soft, pedunculated, flesh-coloured to lightly hyperpigmented papule, occurring in intertriginous and friction-bearing sites (neck, axillae, eyelids, groin, inframammary fold). Acrochordons are essentially universal in adulthood, increasing in number with age, obesity, type 2 diabetes, insulin resistance and pregnancy. They are entirely benign with no malignant potential. The skin-oncology relevance lies in two contexts: (1) the rare confusion with pedunculated melanoma, BCC, neurofibroma or other neoplasm — biopsy any unusually sized, pigmented, growing or atypical lesion; and (2) the recognition that multiple acrochordons in unusual sites in a young patient can be an early marker of Birt-Hogg-Dubé syndrome (FLCN — fibrofolliculomas + pulmonary cysts + RCC), where the "skin tags" are histologically and molecularly fibrofolliculomas. Multiple acrochordons are also associated with insulin resistance and metabolic syndrome — a paraneoplastic-like marker of glucose dysregulation rather than malignancy.

CurrentLast reviewed 26 April 2026
Clinical image of Acrochordon (skin tag)
Acrochordon (skin tag). Image sourced from DermNet New Zealand. Used under CC BY-NC-ND 4.0. No endorsement implied.

Clinical features

  • Soft, pedunculated, flesh-coloured to lightly hyperpigmented papule, 1–5 mm (occasionally larger).
  • Slow-growing; asymptomatic until traumatised, twisted (haemorrhagic infarction → black tag) or caught on clothing.
  • Distribution — neck, axillae, eyelids, groin, inframammary fold; occasionally face / trunk.
  • Median age — adults; prevalence rises steeply with age, reaching universal in older adults.
  • Associations:
    • Obesity, type 2 diabetes, insulin resistance, metabolic syndrome.
    • Pregnancy (often regress post partum).
    • Acromegaly.
    • Acanthosis nigricans (frequently co-exist).
  • Variants — broad-based fibroma molle, filiform / threadlike, pedunculated.

Differential diagnosis

  • Most acrochordons are clinically obvious; biopsy is unnecessary.
  • Biopsy if any of the following:
    • Unusually large size (>1 cm).
    • Pigmentation (especially asymmetric or atypical) — to exclude melanoma.
    • Friable / bleeding / ulcerated.
    • Rapid growth.
    • Indurated base.
    • Diagnostic uncertainty.
  • Differentials — pedunculated seborrhoeic keratosis, polypoid pyogenic granuloma, polypoid melanoma (pedunculated melanoma exists and is regularly missed clinically), pedunculated BCC, neurofibroma (NF1 marker — "buttonhole" sign on palpation), fibrofolliculoma of Birt-Hogg-Dubé (multiple skin-tag-like papules on face / neck / upper trunk in a young to middle-aged patient — see monograph), filiform wart.

Multiple acrochordons → consider underlying conditions

  • Birt-Hogg-Dubé syndrome — multiple skin-tag-like papules that are frequently fibrofolliculomas / trichodiscomas on histology; in young to middle-aged patients with face / neck / upper trunk distribution. Always consider in any patient with dozens of acrochordons appearing before age 40 — see monograph.
  • Insulin resistance / metabolic syndrome — multiple acrochordons are an independent marker; consider HbA1c screening.
  • Acromegaly — multiple skin tags + soft-tissue overgrowth + facial coarsening.
  • Cowden syndrome — among multiple cutaneous markers, but trichilemmomas and palmoplantar pits are more characteristic; see monograph.

Management

  • Reassurance — typical asymptomatic skin tags require no treatment.
  • Removal options (cosmetic / functional / persistently irritated):
    • Snip excision with iris scissors at the base — quick, simple, most common; minimal bleeding.
    • Cryotherapy.
    • Electrodesiccation / cautery.
    • Ligation.
    • Laser ablation.
  • Histology should be performed if any clinical doubt about diagnosis.
  • Multiple acrochordons in a young patient — consider syndromic context (Birt-Hogg-Dubé, Cowden), insulin resistance screening, acromegaly screen if other features.
  • Counsel on weight management / glycaemic control if metabolic context.

References

  1. Akpinar F, Dervis E. Association of skin tag with insulin resistance and metabolic syndrome. N Am J Med Sci; 2012.
  2. Sand FL, Thomsen SF. Skin tags — review. Dermatology; 2018.

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