Idiopathic palmar fasciitis and polyarthritis syndrome
نویسندگان
چکیده
منابع مشابه
Idiopathic Palmar Fasciitis with Polyarthritis Syndrome
A 31-yr-old Korean woman was presented with 4-month history of bilateral hand swelling and stiffness. On clinical examination, she had a painful synovitis of both hands, wrists, knees and ankles. The radiologic and histological examinations confirmed it with palmar fasciitis and polyarthritis syndrome (PFPAS). PFPAS is an uncommon disorder characterized by progressive flexion contractures of bo...
متن کاملParaneoplastic palmar fasciitis and polyarthritis syndrome.
Palmar fasciitis and polyarthritis syndrome is a rare paraneoplastic syndrome that has been reported mainly for ovarian cancers. It is thought to be a tumour-associated autoimmune disorder. It is associated with polyarthritis and rapid flexion contractures of hands with palmar nodules due to palmar fasciitis. Similar paraneoplastic features in gastric cancers have seldom been reported. Here, I ...
متن کاملPalmar fasciitis and polyarthritis as a paraneoplastic syndrome associated with tubal carcinoma: a case report.
A 73 year old white woman was admitted to our hospital in May 2003 complaining of lower abdominal pain for 1 month. On admission, the gynaecological examination disclosed a large, non-tender lower abdominal mass of 7 cm in diameter, which was highly suspicious of ovarian cancer with peritoneal infiltration in the computed tomography scan. In accordance with these findings, serum levels of CA 12...
متن کاملPalmar fasciitis and arthritis syndrome associated with metastatic ovarian cancer: a paraneoplastic syndrome.
Palmar fasciitis and polyarthritis syndrome (PFPA) is an uncommon syndrome that affects predominantly elderly women and characterized by symmetrical polyarthritis followed by flexioncontracture of the hands. It is usually associated with a metastatic malignant neoplasm, and therefore implies a poor prognosis. We report a case of a 54-year old woman presented with palmar fasciitis and polyarthri...
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Idiopathic hypereosinophilic syndrome is a multisystem disease with peripheral blood eosinophilia of at least 6 months duration, multiple organ system involvement, and no evidence for other known causes of eosinophilia. It is characteristically a disease of middle-aged men, often has a poor prognosis and is seldom found during childhood. Heart dicsease, characterized by endomyocardial fibrosis ...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2019
ISSN: 1757-790X
DOI: 10.1136/bcr-2019-232954