scleromyxedema is a rare, chronic, progressive, fibromucinous disorder of unknown etiology, characterized by lichenoid waxy papules and firm induration of skin of trunk, face, forearm and hands; fibroblast proliferation and mucin deposition in the upper dermis. cutaneous involvement is characteristic but there are several associated systemic manifestations: we observed a case of scleromyxedema ...

CMI: cutaneous mucinosis of infancy SHJCM: self-healing juvenile cutaneous mucinosis W e present a case of a 4-year-old fairskinned girl, with no significant medical history, who presented to the outpatient clinic of an academic medical center with an asymptomatic, flesh-colored, cobblestoned plaque on her lateral left thigh (Fig 1). Per the family’s report, the lesion had grown significantly s...

Discussion | In 1995, Benchikhi et al4 reported the first case of cutaneous B-cell lymphoma associated with follicular mucinosis in a patient with bone-marrow and peripheral blood infiltration.4We report the first caseof primary cutaneous follicle center lymphoma with follicular mucinosis. Cutaneous lymphomascanusuallybedistinguishedbyarchitectural features, where most atypical lichenoid infilt...

Lichen myxedematosus, or papular mucinosis, is a skin disorder characterized by accumulation of mucin in the dermis. We present the case of a patient with HIV infection and lichen myxedematosus whose skin condition completely resolved with antiretroviral therapy.