Results 61 to 70 of about 5,114 (228)
Extragenital lichen sclerosus et atrophicus
Dermatology Online Journal, 2008 A 76-year-old woman with a history of eczematous dermatitis presented with a 9-month history of a pruritic, eczematous eruption of the trunk. This eruption responded to topical glucocorticoids but recurred on discontinuation of treatment on multiple occasions. A biopsy specimen showed extragenital lichen sclerosus et atrophicus.
Bergstrom, Kendra G +3 more
openaire +4 more sources
The use of human adipose-derived stem cells in the treatment of physiological and pathological vulvar dystrophies [PDF]
, 2016 “Vulvar dystrophy” is characterized by chronic alterations of vulvar trophism, occurring in both physiological (menopause) and pathological (lichen sclerosus, vulvar graft-versus-host disease) conditions.
CARELLA, SARA +4 more
core +4 more sources
Matrix metalloproteinase 9 (MMP-9) is differently expressed in cutaneous lichen planus and lichen sclerosus [PDF]
, 2012 Lichen planus is a mucocutaneous inflammatory disease of unknown etiology. Hyperkeratosis, focal hypergranulosis, damage to the basal cell layer, and bandlike infiltrate are hallmarks of LP skin.
Groma, Valerie, Legusa, Ilze
core +3 more sources
Human Pathology Reports, 2021 A 67-year-old woman presented with a 2 x 1.5 cm white, asymptomatic verrucous plaque on the left labia minora. She was known for vulvar lichen sclerosus et atrophicus (LSA) for 1.5 years, treated with high-potency topical corticosteroids. A biopsy of the
Simon F. Roy, Jahg Wong, Kurosh Rahimi
doaj +1 more source
Unexpected high frequency of genital involvement in women with clinical and hostological features of oral lichen planus [PDF]
, 2006 The main aims of this cross-sectional study were: (i) to assess the frequency of genital (vulval) lichen planus (VLP) and vulval lichen sclerosus (VLS) in women affected with oral lichen planus (OLP), regardless of the genital symptoms reported; and (ii)
BELFIORE, P +6 more
core +1 more source
Vulvar lichen planus pemphigoides
International Journal of Women's Dermatology, 2017 Lichen planus pemphigoides (LPP) is a rare blistering disease with features of both lichen planus and bullous pemphigoid. LPP typically appears on the extremities and occasionally involves the oral mucosa.
Jameson Loyal, M.D., Shadi Rashtak, M.D.
doaj +1 more source
Anais Brasileiros de Dermatologia, 2014 Idiopathic Atrophoderma of Pasini and Pierini (IAPP) is a rare, exclusively cutaneous disease. It is more frequent in females, with incidence peak in the second and third decades of life. The etiopathogenesis remains unknown.
Carolina Mayana de Avila Batista +4 more
doaj +1 more source
Indian Journal of Dermatopathology and Diagnostic Dermatology, 2019 Background: Genital lichen sclerosus (LS) is a chronic, autoimmune, inflammatory dermatosis of genitalia more common in females than males. Diagnosis of early genital LS is difficult clinically; hence, histopathology may help to confirm the diagnosis ...
Sunanda A Mahajan +3 more
doaj +1 more source
Lichen sclerosus et atrophicus.
Dermatology nursing, 2006 A case of 43-year-old woman with skin and genital lesions of lichen sclerosus et atrophicus was presented. It was paid attention to simultaneously examination of the skin and genital areas. For this reason it is necessary closed cooperation between dermatologists and gynaecologists for determination of proper diagnosis.
Bethany, Cook, Charles E, Crutchfield
+6 more sources
Lichen sclerosus associated with localized scleroderma: dermoscopy contribution [PDF]
Anais Brasileiros de Dermatologia, 2016 : Lichen sclerosus is an uncommon inflammatory dermatosis with preferential involvement of the urogenital region. The extragenital involvement is uncommon and is characterized by small rounded macules or papules, pearly white in color. The coexistence of
Monisa Martins Nóbrega +5 more
doaj +1 more source