Amyloidosis
https://en.wikipedia.org/wiki/Amyloidosis
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Faiga masani o foliga o Amyloidosis

I le vaʻaiga faʻalautele, o papules malo ma foliga tutusa e matauina. E foliga tutusa ma faigata, e le pei o faʻamaʻi faʻamaʻi e pei ole atopic dermatitis.


Fa'aaliga o le pa'u o le amyloidosis cutis dyschromica ― (A) Macules fa'aapopo ma hypopigmented ile vae pito i lalo.

Lichen amyloidosis e masani ona fa'aseseina o le atopic dermatitis. O se tulaga masani e maua i tamai papules malo ma mageso.

O le manu'a o Amyloidosis atonu e pei o le atopic dermatitis.
relevance score : -100.0%
References
Lichen amyloidosis - Case reports 24130236 NIH
Na sau se fafine e 26 tausaga le matua i le matou falemaʻi ma faitio i le mageso o ona vae na maua i le 10 tausaga. E ui i le fa'aaogaina o kulimi steroid ma le kulimi tazarotene, e le'i toe lelei le mageso. E le'i i ai sana tala'aga talafeagai o lona aiga. Ina ua matou su'esu'eina o ia, na matou maua atu i luga o ona vae ua si'i i luga, ma talatala, e fetaui ma se ma'i e ta'ua o le 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: Towards Pathogenesis-Driven Targeted Treatment 36763750 NIH
Lichen Amyloidosis ose ma'i e seasea maua ile pa'u e feso'ota'i ma mageso faifai pea ole mafua'aga. E masani ona aliali a'e o ni fuifui o pa'i fa'atui'i, fa'ailoga lanu ile pito i fafo ole pa'u. Lichen Amyloidosis e masani ona aliali mai i tagata e 50 i le 60 tausaga ma o le mea e leaga ai, e leai se fofo. O togafitiga o lo'o avanoa nei e le masani ona lelei.
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.
Clinical Characteristics of Lichen Amyloidosis Associated with Atopic Dermatitis: A Single Center, Retrospective Study 38086357 NIH
Lichen amyloidosis ose ma'i mageso umi-umi. E lauiloa i fuifui o patupatu mafiafia e masani ona maua i tua, ivi, ogavae, ma lima. Pe a su'esu'eina i lalo ole microscope, Lichen amyloidosis o lo'o fa'aalia ai le fa'aputuina o le amyloid ile pito i luga ole pa'u fa'atasi ai ma le mafiafia ma le fa'ateleina ole pa'u pito i fafo. E ui o le mafuaaga tonu o le Lichen amyloidosis e leʻo malamalama atoatoa i le taimi nei, o suʻesuʻega talu ai na faʻafesoʻotaʻi i mea e pei o le olo poʻo le feteʻenaʻi i luga o le paʻu, cell death, viral infections, ma isi. Lichen amyloidosis e foliga mai e feso'ota'i ma le tele o isi tulaga pa'u (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.
○ Suiga ma Togafiti
#Electrophoresis of blood or urine
#Skin biopsy