ED62.0

ICD-11 MMS 2026-01

Haemosiderin pigmentation of skin

Description

Dermal haemosiderin deposition causes a yellowish-brown or bronze discolouration of the skin. The deposition may be focal as seen following repeated extravasation of red blood cells (e.g. in association with venous hypertension or chronic vasculitis) or from generalised iron overload (e.g. haemochromatosis). Haemosiderin may stimulate melanogenesis and thus the colour is due to variable proportions of haemosiderin and melanin.

Index terms

  • Haemosiderin pigmentation of skin
  • Iron pigmentation
  • iron pigmentation disorder
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  • Lower limb haemosiderosis
  • haemosiderin pigmentation of lower limbs due to chronic venous insufficiency
  • hypostatic haemosiderosis

Sibling codes

  • ED62.Y – Other specified endogenous non-melanin pigmentation
  • ED62.Z – Endogenous non-melanin pigmentation, unspecified

Foundation entity

Haemosiderin pigmentation of skin – http://id.who.int/icd/entity/495802390

Part of: ED62: Endogenous non-melanin pigmentation › 14: Diseases of the skin