[Takayasu's Arteritis and Sweet's Syndrome - a rare combination] [0.03%]
[Takashina动脉炎和Sweet综合征-罕见的组合]
L A Almeida,L M H Mota,R A V Kirchenheim et al.
L A Almeida et al.
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):288-9. DOI: 2009
Sara Lestre,Vasco Serrão,Alexandre João et al.
Sara Lestre et al.
Churg-Strauss syndrome (CSS), also known as allergic granulomatous angiitis, is a rare disorder characterized by the presence of asthma, eosinophilia and small-to-medium sized vessels vasculitis. Vasculitis commonly affects lung, heart, ski...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):281-7. DOI: 2009
Ana Filipa Mourão,Teresa Laura Pinto,Sandra Falcão et al.
Ana Filipa Mourão et al.
Juvenile dermatomyositis (JDM) is a rare systemic disease of unknown etiology characterized by inflammation of the muscle, skin and digestive tract, with variable outcome. The diagnostic criteria include proximal symmetrical muscular weakne...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):276-80. DOI: 2009
[Association between pulmonary hemosiderosis and juvenile dermatomyositis] [0.03%]
肺 hemosiderosis 和幼年皮肌炎的关系
Clarissa Harumi Omori,Adriana A Jesus,Adriana M E Sallum et al.
Clarissa Harumi Omori et al.
Introduction: Pulmonary hemosiderosis (PH) is characterized by recurrent diffuse intra-alveolar hemorrhage associated to the presence of hemosiderin deposits inside macrophages. In the present Pediatric Rheumatology Servi...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):271-5. DOI: 2009
Adelino Carragoso,Bernardo Faria,José Roberto Silva et al.
Adelino Carragoso et al.
Thymus is an important central lymphoid organ that plays a pivotal role in the generation of peripheral T-lymphocytes. Thymoma and thymus hyperplasia have been associated with various autoimmune disorders, mainly myasthenia gravis. There is...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):251-255. DOI: 2009
[Degos' disease as a cutaneous manifestation of systemic lupus erythematosus] [0.03%]
Degos病作为系统性红斑狼疮的皮肤表现病例一例报告
Jozélio Freire de Carvalho
Jozélio Freire de Carvalho
Degos' disease or malignant atrophic papulosis is a rare vasculopathy characterized by the presence of a typical skin lesion and visceral vascular involvement of small vessels, mainly of the digestive tract or central nervous system. The mo...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):246-50. DOI: 2009
M Raquel Marques,Catarina Matos,Susana Oliveira
M Raquel Marques
We present a case of a 28-year-old black female patient with a previous diagnosis of overlapping syndrome of lupus and rheumatoid arthritis, treated with corticosteroids and methotrexate, who was admitted to our department due to abdominal ...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):241-5. DOI: 2009
[Nutritional evaluation and physical functional ability in scleroderma patients] [0.03%]
系统性硬化症患者的营养状况及体能评估
Valderilio Feijó Azevedo,Carolina de Souza Müller,Luciane Rinaldi et al.
Valderilio Feijó Azevedo et al.
Introduction: Systemic Sclerosis (SSc) is an inflammatory disease that decreases functional capacity through muscular atrophy, skin sclerosis and loss of joint function. Scleroderma patients suffer from movement's restric...
[Smell: integrating neurodegeneration and autoimmunity - a personal view] [0.03%]
[嗅觉：神经退行性病变和自身免疫的相互作用——个人见解]
Samuel-Datum Moscavitch,Martine Szyper-Kravitz,Yehuda Shoenfeld
Samuel-Datum Moscavitch
Throughout human evolution, smell lost its important role to be replaced by other senses. Although, it retained a "role"in several "healing" practices. The aim of this review was to analyze the possible roles and influences of olfaction on ...
Ana Ribeiro,José Costa,Mónica Bogas et al.
Ana Ribeiro et al.
Mutilans arthritis is a rare psoriatic arthritis subtype. The authors present 2 cases of psoriatic mutilans arthritis, who pictures of the hands and feet and their radiographies are very representative of a severe, disfigurant and disabilit...
Case Reports
Acta reumatologica portuguesa. 2009 Apr-Jun;34(2A):290-1. DOI: 2009