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Recurrent primary hyperphosphatemic tumoral calcinosis: a case report
Maggad Rangaswamy1, Krishnamurthy Jayashree, Prabhu Saggam
1Department of Pathology, JSS Medical College and Hospital, Ramanuja Road, Mysore, Karnataka 570009, India.
Acta Cytologica
|November 9, 2010
Summary
Tumoral calcinosis (TC) is a rare condition causing extensive calcification in soft tissues, primarily affecting young individuals. This case highlights typical clinical and diagnostic features of TC, emphasizing its obscure etiology.
Area of Science:
- Medical Science
- Pathology
- Radiology
Background:
- Tumoral calcinosis (TC) is a rare idiopathic condition characterized by extensive non-osseous calcification.
- It primarily affects adolescents and young adults, often in periarticular soft tissues of major joints.
Observation:
- A young female patient presented with recurrent subcutaneous swellings.
- Elevated serum phosphorus with normal serum calcium levels were noted.
- Clinical and radiological findings were suggestive of TC.
Findings:
- Cytologic and histopathologic studies confirmed the diagnosis of tumoral calcinosis.
- Positive von-Kossa stain confirmed calcium deposits, solidifying the diagnosis.
- The case presented typical clinical, radiological, and histopathological features of TC.
Implications:
- This case underscores the importance of recognizing the characteristic features of tumoral calcinosis.
- Accurate diagnosis relies on a combination of clinical presentation, imaging, and histopathology.
- Further research into the obscure etiology of TC is warranted.
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