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1,359 Possible Causes for paraspinal calcification

Did you mean: paraspinal, calcification

  • 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[ncbi.nlm.nih.gov] Abstract An 88-year-old woman with CREST syndrome (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasias) presented with hyperglycemia[ncbi.nlm.nih.gov] CONCLUSION: Carbon dioxide laser vaporization may offer effective remission of symptoms in cutaneous calcinosis of CREST syndrome (including cutaneous calcinosis, Raynaud's[ncbi.nlm.nih.gov]

  • Tumoral Calcinosis

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

  • Calcinosis Cutis

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

  • Calcinosis Circumscripta

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

  • Familial Normophosphatemic Tumoral Calcinosis

    Abstract Dystrophic cutaneous calcinosis is associated with disorders as common as autoimmune diseases and cancer.[ncbi.nlm.nih.gov] […] changes Pakasa, NM; Kalengayi, RM Familial tumoral calcinosis.[deepdyve.com] […] tumoral calcinosis, and secondary tumoral calcinosis.[gulfdoctor.net]

  • Calcinosis Universalis

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

  • Calcinosis

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

  • Vitamin D Deficiency

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

  • Childhood Dermatomyositis

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

  • Familial Teutschlaender Disease

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

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