Vascular tumourBenignICD-10 D18.0

Hobnail haemangioma

Targetoid haemosiderotic haemangioma; superficial haemosiderotic lymphovascular malformation; THH

Hobnail haemangioma is a benign vascular lesion that classically presents as a solitary red-brown to violaceous papule surrounded by a pale halo and an outer ecchymotic ring — the targetoid appearance that gave it its alternative name (targetoid haemosiderotic haemangioma). It is a frequent clinical mimic of melanoma and Kaposi sarcoma because of the dark central papule and surrounding pigment, and is often excised as a precaution. Histologically it shows characteristic "hobnail" endothelial cells with apical nuclei protruding into vessel lumina, accompanied by dermal haemosiderin deposition. Benign with no metastatic potential.

CurrentLast reviewed 15 May 2026

Clinical features

  • Solitary red-brown to violaceous papule, 5–15 mm.
  • Targetoid appearance — central dark papule + pale halo + outer ecchymotic ring (haemosiderin deposition).
  • Common sites — trunk, extremities; rarely face.
  • Median age 25–45; both sexes; often history of mild trauma to the area.
  • Slow growth over months; ecchymotic features may fluctuate.
  • Often clinically misdiagnosed as melanoma, Kaposi sarcoma, dermatofibroma or pyogenic granuloma — excisional biopsy is the rule.

Histology

  • Biphasic vascular proliferation:
    • Superficial dilated thin-walled vessels with characteristic "hobnail" endothelial cells — flattened cells with apical nuclei bulging into lumina like tacks.
    • Deeper slit-like vessels in collagen.
  • Dermal haemosiderin and erythrocyte extravasation responsible for the ecchymotic ring.
  • Immunohistochemistry — CD31, ERG positive; D2-40 / podoplanin positive in some (suggesting lymphatic differentiation in part).
  • Differential — Kaposi sarcoma (HHV-8 / LANA-1 positive), microvenular haemangioma, retiform haemangioendothelioma (more aggressive).

Management

  • Excisional biopsy — diagnostic and definitive.
  • Histology confirms benign nature; reassurance.
  • Recurrence after complete excision uncommon.
  • Multiple lesions or atypical features — consider retiform haemangioendothelioma (more aggressive); specialist review.

References

  1. Santa Cruz DJ, Aronberg J. Targetoid hemosiderotic hemangioma. J Am Acad Dermatol; 1988.
  2. Mentzel T et al. Hobnail hemangioma — clinicopathologic, immunohistochemical study. J Cutan Pathol; 1999.

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