Characterized by large, asymptomatic, sharply demarcated 'cliff-drop' patches of dermal atrophy with a bluish-brown hue and no sclerosis, distinguishing it from morphea.
A deep burn heals with a hypertrophic or keloidal scar that is firm, indurated, and contracted.
A rare form of cutaneous metastasis, typically from breast cancer, where the skin of the chest becomes diffusely infiltrated, sclerotic, and board-like.
A rare scleroderma-like disorder with rapid onset of symmetric, painful swelling and induration of the limbs, sparing the hands and feet, and associated with peripheral eosinophilia.
Presents as atrophic, porcelain-white plaques, which are less indurated than morphea.
An overgrowth of scar tissue that extends beyond the borders of the original wound, forming a firm, rubbery, indurated nodule or plaque.
A form of primary cutaneous amyloidosis with intensely pruritic, hyperkeratotic papules that coalesce into thickened, indurated, brownish, rippled plaques on the shins.
A panniculitis presenting as firm, deep, subcutaneous nodules that are indurated but heal with a characteristic depressed scar.
A form of primary cutaneous amyloidosis with pruritic, grayish-brown macules that have a rippled pattern, which is not typically indurated.
A form of localized scleroderma presenting as a well-demarcated, indurated, sclerotic plaque that becomes ivory-white and atrophic, often with a lilac-colored border.
A condition on the shins where plaques develop a distinct waxy, yellow, atrophic center with a raised, indurated border.
A fibrosing disorder in patients with renal failure exposed to gadolinium, causing symmetric, woody induration and brawny hyperpigmentation of the limbs.
A paraneoplastic syndrome where skin changes include diffuse hyperpigmentation, hypertrichosis, and skin thickening or sclerosis.
A manifestation of Graves' disease, with symmetric, non-pitting, firm, indurated plaques and nodules on the shins with a peau d'orange texture.
A condition with symmetric, non-pitting, woody induration of the skin, typically starting on the neck and upper back, without the papules of scleromyxedema.
A chronic form of GVHD that closely mimics systemic sclerosis, with hidebound, sclerotic skin and joint contractures.