Amyloidosis - Amyloidose
☆ Tamin'ny valin'ny Stiftung Warentest 2022 avy any Alemaina, ny fahafaham-pon'ny mpanjifa amin'ny ModelDerm dia ambany kely noho ny fifampidinihana telemedicine karama.
endri-tarehy mahazatra an'ny Amyloidose (Amyloidosis)
References
Nisy vehivavy 26 taona tonga teny amin’ny tobim-pahasalamanay nitaraina noho ny ratra mangidihidy teo amin’ny tongony efa 10 taona izay. Na dia teo aza ny fampiasana crème steroid sy tazarotene, dia tsy nety tsara ilay maimaika. Tsy nanana tantaram-pianakaviana mifandraika amin'izany izy. Rehefa nozahanay izy, dia hitanay fa nisy tampina mihodinkodina teo anoloan'ny tongony, izay mifanaraka amin'ny aretina antsoina hoe lichen amyloidosis.
A 26-year-old woman presented to our clinic with an itchy rash on her legs that had persisted for 10 years. The rash had previously been treated with topical steroids and tazarotene cream, with no improvement. The patient’s family history was noncontributory. A physical examination showed discrete and coalescing hyperkeratotic tan-brown papules on the pretibial surfaces, consistent with lichen amyloidosis.
A 26-year-old woman presented to our clinic with an itchy rash on her legs that had persisted for 10 years. The rash had previously been treated with topical steroids and tazarotene cream, with no improvement. The patient’s family history was noncontributory. A physical examination showed discrete and coalescing hyperkeratotic tan-brown papules on the pretibial surfaces, consistent with lichen amyloidosis.
Lichen Amyloidosis dia aretina hoditra tsy fahita firy mifandray amin'ny mangidihidy maharitra tsy fantatra ny antony. Matetika izy io no miseho amin'ny fitambarany misy tasy mitsangana sy miloko eo amin'ny faritra ivelany amin'ny hoditra. Lichen Amyloidosis dia miseho matetika amin'ny olona 50 ka hatramin'ny 60 taona ary indrisy fa tsy misy fanafodiny. Tsy mandeha tsara ny fitsaboana misy ankehitriny.
Lichen Amyloidosis (LA) is an uncommon, primary cutaneous amyloidosis associated with chronic, idiopathic pruritus. Clinical presentation of LA includes skin colored to hyperpigmented, papules coalescing into plaques with a rippled appearance on the extensors.1 LA most commonly presents in the fifth to sixth decade of life and has no curative treatments. Overall response to current therapies is poor.
Lichen Amyloidosis (LA) is an uncommon, primary cutaneous amyloidosis associated with chronic, idiopathic pruritus. Clinical presentation of LA includes skin colored to hyperpigmented, papules coalescing into plaques with a rippled appearance on the extensors.1 LA most commonly presents in the fifth to sixth decade of life and has no curative treatments. Overall response to current therapies is poor.
Lichen amyloidosis dia aretina hoditra mangidihidy maharitra. Izy io dia fantatra amin'ny fitambaran'ny fivontosana matevina hita indrindra eo amin'ny lamosina, ny hodiny, ny feny ary ny sandry. Rehefa dinihina amin'ny alalan'ny mikraoskaopy, Lichen amyloidosis dia mampiseho fivondronan'ny amyloid eo amin'ny sosona ambony amin'ny hoditra miaraka amin'ny fanatevenana sy ny fanitarana ny sosona hoditra ivelany. Na dia mbola tsy fantatra tsara aza ny tena anton'ny Lichen amyloidosis , ny fanadihadiana teo aloha dia nampifandray izany tamin'ny antony toy ny fikikisana na fikitihana amin'ny hoditra, ny fahafatesan'ny sela, ny areti-mifindra, sns. Lichen amyloidosis dia toa mifandray amin'ny aretina hoditra maro hafa (atopic dermatitis, lichen planus, mycosis fungoides) .
Lichen amyloidosis (LA) is a chronic pruritic skin disorder characterized by multiple grouped hyperkeratotic papules, predominantly located on the back, shins, thighs, and arms. Histological analysis of LA shows amyloid deposition in the papillary dermis and hyperkeratosis and acanthosis of the epidermis. The exact pathogenesis of LA has not yet been elucidated; however, prior reports have implicated frictional epidermal damage, apoptosis, viral infection, and many other triggers. LA is reportedly associated with several skin disorders, including atopic dermatitis (AD), lichen planus, and mycosis fungoides.
Lichen amyloidosis (LA) is a chronic pruritic skin disorder characterized by multiple grouped hyperkeratotic papules, predominantly located on the back, shins, thighs, and arms. Histological analysis of LA shows amyloid deposition in the papillary dermis and hyperkeratosis and acanthosis of the epidermis. The exact pathogenesis of LA has not yet been elucidated; however, prior reports have implicated frictional epidermal damage, apoptosis, viral infection, and many other triggers. LA is reportedly associated with several skin disorders, including atopic dermatitis (AD), lichen planus, and mycosis fungoides.
○ Diagnose sy Fitsaboana
#Electrophoresis of blood or urine
#Skin biopsy