Amyloidosishttps://en.wikipedia.org/wiki/Amyloidosis
☆ A cikin sakamakon Stiftung Warentest na 2022 daga Jamus, gamsuwar mabukaci tare da ModelDerm ya ɗan yi ƙasa kaɗan fiye da biyan shawarwarin telemedicine. Classic fuskokin fuska Amyloidosis
A cikin haɓakar ra'ayi, ana ganin papules masu wuya masu kama da siffa. Suna da ɗanɗano iri ɗaya kuma suna da wuyar gaske, sabanin cututtukan rashin lafiyan irin su atopic dermatitis.
Fatar jikin amyloidosis cutis dyschromica ― (A) Macules masu launin fata da masu launin fata a ƙasan kafa
Lichen amyloidosis yawanci ana kuskuren ganewa a matsayin atopic dermatitis. Halin da aka saba yana nunawa tare da ƙananan papules mai wuya da itching.
Cutar Amyloidosis na iya kama da na atopic dermatitis.
relevance score : -100.0%
References Lichen amyloidosis - Case reports 24130236 NIH
Wata mata ‘yar shekara 26 ta zo asibitinmu tana korafin wani kurji da ta yi a kafafunta da ta yi shekara 10. Duk da yin amfani da kirim na steroid da kirim na tazarotene, kurji bai yi kyau ba. Ba ta da wani tarihin dangi da ya dace. Da muka duba ta, sai muka tarar da tarkace a gaban kafafunta, wadanda suka yi daidai da wata cuta mai suna 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 cuta ce da ba kasafai ake samun fata ba wacce ke da alaƙa da ƙaiƙayi na dindindin wanda ba a san dalili ba. Yawanci yana nunawa azaman gungu na ɗimbin faci, waɗanda ba su da launi a saman saman fata. Lichen Amyloidosis yawanci yana bayyana a cikin mutane masu shekaru 50 zuwa 60 kuma abin takaici, babu magani. Jiyya da ake samu yanzu ba kasafai suke aiki da kyau ba.
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 ciwon fata ne mai dadewa. An san shi ga gungu masu kauri waɗanda aka fi samu a baya, shins, cinyoyi, da hannaye. Lokacin da aka bincika a ƙarƙashin na'urar hangen nesa, Lichen amyloidosis yana nuna tarin amyloid a saman Layer na fata tare da kauri da haɓakar fatar fata. Duk da cewa har yanzu ba a fahimci ainihin abin da ke haifar da Lichen amyloidosis ba, binciken da aka yi a baya ya danganta shi da abubuwa kamar shafa ko gogayya a fata, mutuwar kwayar halitta, kamuwa da kwayar cutar hoto, da sauransu. Lichen amyloidosis alama yana da alaƙa da wasu yanayin fata (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.
○ Diagnosis da Magani
#Electrophoresis of blood or urine
#Skin biopsy