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1,359 Possible Causes for paraspinal calcification

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  • Limited Cutaneous Systemic Sclerosis

    Abstract We describe a patient with a 23-year history of progressive calcinosis and features of the CREST syndrome (calcinosis, Raynaud's phenomenon, esophageal dysmotility[] Abstract An 88-year-old woman with CREST syndrome (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasias) presented with hyperglycemia[] CONCLUSION: Carbon dioxide laser vaporization may offer effective remission of symptoms in cutaneous calcinosis of CREST syndrome (including cutaneous calcinosis, Raynaud's[]

  • Tumoral Calcinosis

    Tumoral calcinosis is characterized by tumor-like deposition of calcium in periarticular soft tissue.[] calcinosis, and secondary tumoral calcinosis.[] Tumoral calcinosis is rarely located in spine.[]

  • Calcinosis Cutis

    Sometimes a surgical intervention, especially in paraspinal calcifications, may be necessary.[] CONCLUSIONS: Radiography detected calcinosis in all patients and is recommended for initial imaging of calcinosis.[] PATIENTS: Seventy-eight patients with calcinosis cutis and ACTD between 1996 and 2009.[]

  • Calcinosis Circumscripta

    To our knowledge, these are the first patients with calcinosis circumscripta treated by hip arthroscopy.[] She was then treated with probenecid up to 2 g daily and her calcinosis lessened steadily over three years.[] Digital calcinosis circumscripta is an unusual form of calcinosis circumscripta occurring specifically in the digits.[]

  • Familial Normophosphatemic Tumoral Calcinosis

    Abstract Dystrophic cutaneous calcinosis is associated with disorders as common as autoimmune diseases and cancer.[] […] changes Pakasa, NM; Kalengayi, RM Familial tumoral calcinosis.[] […] tumoral calcinosis, and secondary tumoral calcinosis.[]

  • Calcinosis Universalis

    Different treatments have been used in an attempt to clear calcinosis lesions and prevent its recurrence but none has been clearly effective.[] Four patients with calcinosis universalis were treated with 1 mg per day of warfarin for 18 months in a non-blind initial study.[] Calcium deposits in soft tissues without previous trauma may represent calcinosis universalis, a condition without systemic manifestations and with laboratory values of blood[]

  • Calcinosis

    Cervical paraspinal calcification in collagen vascular diseases. AJR Am J Roentgenol 1991; 157, pp 523–525. 5.[] RESULTS: There were 215 SSc patients, including 65 SSc-calcinosis (81.5% females) and 150 SSc-without calcinosis (controls, 77% females).[] […] development of calcinosis in these patients.[]

  • Vitamin D Deficiency

    The management implications and effect of vitamin D deficiency on phosphate metabolism in the setting of tumoral calcinosis is discussed.[] The clinical, radiological, and biochemical profile confirmed the diagnosis of tumoral calcinosis. She also had associated vitamin D deficiency.[]

  • Childhood Dermatomyositis

    No coexistence of FOP and childhood dermatomyositis with calcinosis was found.[] These were followed by myopathic changes on EMG, calcinosis, dysphonia and nailfold capillaroscopy, which were ranked equally.[] Calcinosis, while helpful if present, occurs in only a minority of cases, sometimes late in the disease course.[]

  • Familial Teutschlaender Disease

    calcinosis (HFTC) is known to be caused by mutations in at least three genes: FGF23, GALNT3 and KL.[] […] and dystrophic calcinosis.[] Name Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 Synonyms CALCINOSIS, TUMORAL, WITH HYPERPHOSPHATEMIA, CORTICAL HYPEROSTOSIS WITH HYPERPHOSPHATEMIA, HYPEROSTOSIS WITH[]

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