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Subacute cutaneous lupus erythematosus Classification and external resources ICD-10 L93.1 MeSH D008178 Subacute cutaneous lupus erythematosus is a clinically distinct subset of cases of lupus erythematosus that is most often present in white women aged 15 to 40, consisting of skin lesions that are scaly and evolve as polycyclic annular lesions or psoriasiform plaques.[1] Characteristically the lesions appear in sun-exposed areas such as the vee of the neckline or the forearms, but not the face. It may be brought on by sun-sensitizing medications, but is usually associated with autoimmune disorders such as rheumatoid arthritis and Sjögren's syndrome.[2] Treatment generally involves sun avoidance/protection and topical corticosteroids. [2] Lesions of SCLE may have an annular configuration, with raised red borders and central clearing.[3][4] See also Lupus erythematosus List of cutaneous conditions References ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Page 160. ISBN 0-7216-2921-0. ^ a b Burkhalter NW, McKenzie JT, Lane JE (2009). "Subacute cutaneous lupus erythematosus". Consultant 49 (3). http://www.consultantlive.com/display/article/10162/1387795.  ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 563. ISBN 1-4160-2999-0.  ^ [[:Template:Cite journal]] v • d • e Cutaneous keratosis, ulcer, atrophy, and necrobiosis (L82-L94, 700-701.5) Epidermal thickening/ keratoderma/ keratosis/ hyperkeratosis PPK Inherited diffuse: Diffuse epidermolytic palmoplantar keratoderma • Diffuse nonepidermolytic palmoplantar keratoderma • Palmoplantar keratoderma of Sybert • Mal de Meleda • syndromic (connexin (Bart–Pumphrey syndrome • Clouston's hidrotic ectodermal dysplasia • Vohwinkel syndrome) • Corneodermatoosseous syndrome • plakoglobin (Naxos syndrome) • Scleroatrophic syndrome of Huriez • Olmsted syndrome • Cathepsin C (Papillon–Lefèvre syndrome • Haim–Munk syndrome) • Camisa disease focal: Focal palmoplantar keratoderma with oral mucosal hyperkeratosis • Focal palmoplantar and gingival keratosis • Howel–Evans syndrome • Pachyonychia congenita (Pachyonychia congenita type I • Pachyonychia congenita type II)  • Striate palmoplantar keratoderma • Tyrosinemia type II) punctate: Acrokeratoelastoidosis of Costa • Focal acral hyperkeratosis • Keratosis punctata palmaris et plantaris • Keratosis punctata of the palmar creases • Schöpf–Schulz–Passarge syndrome • Porokeratosis plantaris discreta • Spiny keratoderma ungrouped: Palmoplantar keratoderma and spastic paraplegia • desmoplakin (Carvajal syndrome) • connexin (Erythrokeratodermia variabilis • HID/KID) Acquired Keratoderma climactericum • Paraneoplastic keratoderma • Acrokeratosis paraneoplastica of Bazex • Aquagenic keratoderma Other Acanthosis nigricans · Keloid · Seborrheic keratosis · Callus • Keratoderma blennorrhagica • Ichthyosis acquisita Skin ulcer Pyoderma gangrenosum Atrophic/atrophoderma Lichen sclerosus · Anetoderma (Schweninger–Buzzi anetoderma, Jadassohn–Pellizzari anetoderma) · Atrophoderma of Pasini and Pierini · Acrodermatitis chronica atrophicans · Semicircular lipoatrophy · Follicular atrophoderma · Linear atrophoderma of Moulin Necrobiosis/granuloma necrobiotic/palisading: Granuloma annulare (Perforating, Generalized, Subcutaneous, Granuloma annulare in HIV disease, Localized granuloma annulare, Patch-type granuloma annulare) · Necrobiosis lipoidica · Annular elastolytic giant cell granuloma · Granuloma multiforme · Necrobiotic xanthogranuloma · Palisaded neutrophilic and granulomatous dermatitis · Rheumatoid nodulosis foreign body granuloma: Silica granuloma miscellaneous/other: Granuloma faciale · Sclerosing lipogranuloma · Pyogenic granuloma · Interstitial granulomatous drug reaction · Interstitial granulomatous dermatitis Localized CTD Cutaneous lupus erythematosus chronic: Discoid · Panniculitis subacute: Neonatal ungrouped: Chilblain · Lupus erythematosus–lichen planus overlap syndrome · Tumid · Verrucous · Rowell's syndrome Scleroderma/ Morphea Localized scleroderma (Localized morphea, Morphea–lichen sclerosus et atrophicus overlap, Generalized morphea, Atrophoderma of Pasini and Pierini, Pansclerotic morphea, Morphea profunda, Linear scleroderma) Other Calcinosis cutis · Sclerodactyly · Poikiloderma vasculare atrophicans · Ainhum/Pseudo-ainhum Transepidermal elimination Kyrle disease · Reactive perforating collagenosis · Elastosis perforans serpiginosa M: INT, SF, LCT anat/phys/devp noco(i,b,d,q,u,r,p,k,c,v)/cong/tumr(n,e,d), sysi/epon proc, drug (D2/3/4/5/8) This cutaneous condition article is a stub. You can help Wikipedia by expanding it. v • d • e