Tumoral calcinosis is a phosphocalcic metabolism anomaly, particularly among younger age groups and characterized by the presence of calcified masses in the juxta-articular regions (hip, elbow, ankle and scapula) without joint involvement. Histologically, lesions dysplay collagen necrobiosis, followed by cyst formation and a foreign-body response with calcification Two forms of tumoral calcinosis have been described: normocalcemic tumoral calcinosis and familial tumoral calcinosis.
frontonasal dysplasia with alopecia and genital anomaly
functioning endocrine neoplasm +
Genetic bone tumor +
Genetic cardiac tumor
Genetic digestive tract tumor +
Genetic endocrine tumor +
Genetic eye tumor
Genetic gynecological tumor +
Genetic renal tumor +
Genetic skin tumor +
Genetic soft tissue tumor +
Genetic tumor of hematopoietic and lymphoid tissues +