Cargando…

Association of amyloidosis cutis dyschromica and familial Mediterranean fever

Amyloidosis cutis dyschromica is a rare type of primary cutaneous amyloidosis characterized by reticulate hyper-pigmentation with discrete hypopigmented macules. Up to date, about 50 cases of amyloidosis cutis dyschromica have been reported and the majority are familial cases of Asian ethnicity. Var...

Descripción completa

Detalles Bibliográficos
Autores principales:	Belli, Asli Akin, Kara, Asude, Dere, Yelda, Yilmaz, Nevin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade Brasileira de Dermatologia 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726667/ https://www.ncbi.nlm.nih.gov/pubmed/29267436 http://dx.doi.org/10.1590/abd1806-4841.20176114

Ejemplares similares

Amyloidosis cutis dyschromica
por: Kurian, Swetha S., et al.
Publicado: (2013)

Amyloidosis cutis dyschromica
por: Qiao, Jianjun, et al.
Publicado: (2012)

Familial Amyloidosis Cutis Dyschromica in Three Siblings: Report from Indonesia
por: Hermawan, Melyawati, et al.
Publicado: (2014)

Amyloidosis cutis dyschromica in two female siblings: cases report
por: Yang, Wenlin, et al.
Publicado: (2011)

Amyloidosis Cutis Dyschromica: A Rare Reticulate Pigmentary Dermatosis
por: Verma, Shyam, et al.
Publicado: (2015)

A Case of Leukemia Cutis with Acute Myeloid Leukemia on Azacitidine Therapy
por: Kara, Asude, et al.
Publicado: (2017)

Deferasirox-induced urticarial vasculitis in a patient with myelodysplastic syndrome
por: Polat, Asude Kara, et al.
Publicado: (2017)

Amyloidosis Cutis Dyschromica in a 16-Year-Old Filipino Girl: A Case Report
por: Bautista, Fendi EJ R., et al.
Publicado: (2022)

Amyloidosis Cutis Dyschromica, A Rare Subtype of Primary Cutaneous Amyloidosis: Case Report and Literature Review
por: Sakhiya, Jagdish, et al.
Publicado: (2021)

Case Report: Amyloidosis Cutis Dyschromica: Dermoscopy and Reflectance Confocal Microscopy and Gene Mutation Analysis of a Chinese Pedigree
por: Wang, Hui, et al.
Publicado: (2021)

Acute Monoblastic Leukemia Presenting with Multiple Granulocytic Sarcoma Nodules
por: Kara, Asude, et al.
Publicado: (2017)

A Rare Presentation of Familial Mediterranean fever; Acute Scrotum and Hydrocele Amyloidosis
por: Yilmaz, Resul, et al.
Publicado: (2010)

Renal amyloidosis due to familial mediterranean fever misdiagnosed
por: Hama, Iman, et al.
Publicado: (2012)

The First Case of Familial Mediterranean Fever Associated with Renal Amyloidosis in Korea
por: Koo, Kyo Yeon, et al.
Publicado: (2012)

Pustular eruption induced by etanercept in a patient with ankylosing spondylitis: a rare side effect
por: Kara, Asude, et al.
Publicado: (2015)

AA Amyloidosis and Atypical Familial Mediterranean Fever with Exon 2 and 3 Mutations
por: Yabuuchi, Junko, et al.
Publicado: (2017)

Renal and suprarenal insufficiency secondary to familial Mediterranean fever associated with amyloidosis: a case report
por: Toros, Ahmet Burak, et al.
Publicado: (2011)

The experience of canakinumab in renal amyloidosis secondary to Familial Mediterranean fever
por: Sozeri, Betul, et al.
Publicado: (2016)

Amyloidosis and Glomerular Diseases in Familial Mediterranean Fever
por: Siligato, Rossella, et al.
Publicado: (2021)

Familial Mediterranean Fever Complicated by a Triad of Adrenal Crisis: Amyloid Goiter and Cardiac Amyloidosis
por: Abukhalaf, Sadi A., et al.
Publicado: (2020)

Familial Mediterranean Fever without Fever
por: Hotta, Yuma, et al.
Publicado: (2020)

Menorrhagia due to uterine amyloidosis in familial Mediterranean fever: case-based review
por: Cansu, Döndü Üsküdar, et al.
Publicado: (2020)

Evaluation of E148Q and Concomitant AA Amyloidosis in Patients with Familial Mediterranean Fever
por: Arici, Zehra Serap, et al.
Publicado: (2021)

A rare cause of fever in an adult: a case of familial Mediterranean fever
por: Erdem, Ilknur, et al.
Publicado: (2018)

Cardiovascular disease risk assessment in patients with familial Mediterranean fever related renal amyloidosis
por: Romano, Micol, et al.
Publicado: (2020)

Secondary bladder amyloidosis with familial Mediterranean fever in a living donor kidney transplant recipient: a case report
por: Imamura, Sentaro, et al.
Publicado: (2016)

Assessment of thyroid disorders in patients with rosacea: a large case-control study()()
por: Akin Belli, Asli, et al.
Publicado: (2021)

Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report
por: Peces, Ramón, et al.
Publicado: (2017)

Atypical Familial Mediterranean Fever Complicated with Gastrointestinal Amyloidosis Diagnosed due to Paroxysmal Arthralgia and Intractable Diarrhea, Successfully Treated with Tocilizumab
por: Aikawa, Erika, et al.
Publicado: (2019)

Posterior Scleritis in Familial Mediterranean Fever
por: Mansour, Ahmad M., et al.
Publicado: (2019)

Is Neutrophil/Lymphocyte Ratio Associated with Subclinical Inflammation and Amyloidosis in Patients with Familial Mediterranean Fever?
por: Uslu, Ali Ugur, et al.
Publicado: (2013)

Familial Mediterranean fever presenting as fever of unknown origin in Korea
por: Lee, Jun Hee, et al.
Publicado: (2016)

Primary systemic amyloidosis, acquired cutis laxa and cutaneous mucinosis in a patient with multiple myeloma
por: Lavorato, Fernanda Guedes, et al.
Publicado: (2013)

Diffuse pulmonary amyloidosis due to Familial Mediterranean Fever, a rare presentation
por: Koksal, Deniz, et al.
Publicado: (2012)

Remission of nephrotic syndrome in amyloidosis of familial Mediterranean fever following colchicine treatment
por: Odabas, Hatice
Publicado: (2006)

Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever
por: Ugurlu, Serdal, et al.
Publicado: (2017)

Transient and Recurrent Pulmonary Infiltrations Associated with Familial Mediterranean Fever
por: Nishiyama, Miho, et al.
Publicado: (2022)

Familial Mediterranean Fever with Small Bowel Stenosis
por: Kasamaki, Keita, et al.
Publicado: (2019)

Rapidly progressive glomerulonephritis in a child with Henoch-Schönlein Vasculitis and familial Mediterranean fever
por: Sozeri, Betul, et al.
Publicado: (2009)

Neurological Face of Familial Mediterranean Fever
por: Bektaş, Polat Cengiz, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_8dnn7oq84qhbvk9dkcrqs4irjt