Displasia fibrosa monostótica em metacarpo – Relato de caso
نویسندگان
چکیده
منابع مشابه
Monostotic fibrous dysplasia: a case report with cone-beam computed tomography findings Displasia fibrosa monostótica: relato de caso por meio de achados de tomografia computadorizada de feixe cônico
Fibrous dysplasia is a benign fibrous-osseous lesion in which normal bone is replaced by fibrous connective tissue and immature bone, affecting only one (monostotic) or several bones (polyostotic) and mainly occurring in children and young adults. When present in facial bones, the maxilla is more frequently involved than the mandible, which can cause facial asymmetry in addition to dental compl...
متن کاملPorocarcinoma - Relato de caso
Eccrine porocarcinoma is a rare, malignant neoplasm of eccrine sweat glands. It often occurs in elderly people, mean age of 67.5 years. The clinical features are variable and their localization is not related to sweat-gland concentration, occurring mainly on the feet and legs. Disease diagnosis and treatment should be as early as possible in order to avoid tumor aggressiveness that occurs in 20...
متن کاملElaioconiose - Relato de caso
Elaioconiosis is a work-rela ted acnei form der ma to sis which affects the expo sed skin of indi vi duals wor king with oils or grea ses. Its inci den ce has decrea sed with the intro duc tion of per so nal pro tec ti ve equip ment, per so nal hygie ne mea su res and the clea ning of work clo thes. Although not a rare disea se, elaio co nio sis is sel dom repor ted in the lite ra tu re, par ti...
متن کاملMixofibrossarcoma - Relato de caso
Myxofibrosarcoma, previously known as malignant fibrous histiocytoma, myxoid variant, is a rare tumor of mesenchymal origin, composed of spindle cells and myxoid stroma. It mainly affects elderly people, involving the lower extremities and frequently extending to the dermis and subcutaneous tissue. The tumor presents high rates of recurrence, and a deep biopsy is required to obtain the correct ...
متن کاملRelato de Caso | Case RepoRt
The authors report no conflicts of interest. AbstrAct Dent’s disease type 1 is an X-linked tubular disease caused by mutations in the renal chloride channel CLCN-5, and it is characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, and renal failure. Several cases have been described in which the only presenting symptoms were asymptomatic proteinuria, and focal segme...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Revista Brasileira de Ortopedia
سال: 2016
ISSN: 0102-3616
DOI: 10.1016/j.rbo.2015.12.007