Literature DB >> 21053587

Recurrent primary hyperphosphatemic tumoral calcinosis: a case report.

Maggad Rangaswamy1, Krishnamurthy Jayashree, Prabhu Saggam, Manjunath Gubbanna Vimala.   

Abstract

BACKGROUND: Tumoral calcinosis (TC) is a special form of idiopathic calcinosis that affects adolescents and young adults. It is characterized by extensive nonosseous calcification, especially in the periarticular soft tissue regions of major joints. CASE: A young girl presented with recurrent subcutaneous swellings over both infrascapular regions and left hip. The patient had elevated serum phosphorus levels while the serum calcium levels were normal. The clinical and radiologic features were suggestive of TC, and the same was confirmed by cytologic and histopathologic study. Positive von-Kossa stain further confirmed that the deposits were of calcium and thus the diagnosis of TC.
CONCLUSION: TC is a disorder of obscure etiology with typical clinical, radiologic, cytologic and histopathologic features.

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Year:  2010        PMID: 21053587

Source DB:  PubMed          Journal:  Acta Cytol        ISSN: 0001-5547            Impact factor:   2.319


  3 in total

1.  Recurrent hyperphosphatemic tumoural calcinosis.

Authors:  Sonal Amit; Asha Agarwal; Anand Nigam; Yashwant Kumar Rao
Journal:  BMJ Case Rep       Date:  2012-09-25

2.  Hyperphosphatemic Tumoral Calcinosis after Total Knee Arthroplasty.

Authors:  Takeshi Mochizuki; Katsunori Ikari
Journal:  Case Rep Orthop       Date:  2017-10-16

3.  Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation-Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency.

Authors:  Sadanandavalli R Chandra; Rita Christopher; Gayathri Narayanappa; Nitin C Ramanujam; Pavan Katragadda; Akshata Huddar; Shreyashi Jha
Journal:  J Pediatr Neurosci       Date:  2018 Jul-Sep
  3 in total

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