2025 Clinician Corner - Unusual radiographic progression of tumoral calcinosis along the anterior cruciate ligament in an adolescent male
Abstract
A 13-year-old boy was referred to orthopedic surgery for chronic intermittent pain and swelling of the left knee. Initial imaging was consistent with osteochondritis dissecans of the femoral condyle. Follow-up imaging demonstrated unexpected progression, with a mass extending into the notch, replacing the anterior cruciate ligament, and eroding the femoral and tibial condyles. Subsequent surgical biopsy and resection revealed tumoral calcinosis, with an ultimate diagnosis of autosomal recessive familial tumoral calcinosis. This case report highlights the radiographic appearance and progression of a rare disease in this unusual location and the differential diagnosis.
Keywords: Adolescent; anterior cruciate ligament; knee; MRI; pediatric; tumoral calcinosis
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Faculty credentials/disclosure
The planners and faculty for this activity have no relevant financial relationships to disclose. The patient consented to the publication of this report.
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Click the "add to cart/begin" button, pay any relevant fee, take the quiz, complete the evaluation, and claim your CME credit. You must achieve 100% on the quiz with unlimited attempts available.
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Expiration date:
Credit eligibility for this article is set to expire on January 1, 2026.
Learning Objectives
After completing the article, the learner should be able to:
- List typical and atypical imaging findings of tumoral calcinosis
- Select the appropriate workup of tumoral calcinosis
- List treatment options for tumoral calcinosis
Key points
Tumoral calcinosis (TC) is a rare disease that typically presents in the periarticular soft tissues along extensor surfaces of large joints in adolescents and young adults, with greater frequency in African-descent populations1,2.
TC may cause pain, swelling, and loss of range of motion of the nearby joint.1
On imaging, TC is typically superficial with calcified lobular masses, layering milk of calcium and/or hemorrhage in cysts on magnetic resonance imaging, and only septal enhancement. Atypical features include bone involvement, intra-articular/extrasynovial joint space involvement, and lack of cysts.1,3–5
Hyperphosphatemic TC, normophosphatemic TC, and secondary causes can usually be discerned with history and biochemical analysis (serum calcium, phosphorus, calcitriol, parathyroid hormone, and renal function tests). If the serum calcium and phosphorus are normal, connective tissue disease should be excluded with a negative antinuclear, anti-Smith, anti-centromere, and anti-scleroderma antibody profile1,6.
- Eric Mastanduono, DDS - Department of Diagnostic Sciences, Texas A&M School of Dentistry, Dallas, Texas, USA
- Farnaz Namazi, DDS - Department of Diagnostic Sciences, Texas A&M School of Dentistry, Dallas, Texas, USA
- Hui Liang, DDS, MS, PhD - Department of Diagnostic Sciences, Texas A&M School of Dentistry, Dallas, Texas, USA and Baylor University Medical Center, Dallas, Texas, USA
- Madhu Nair, BDS, DMD, MS, PhD - Department of Diagnostic Sciences, Texas A&M School of Dentistry, Dallas, Texas, USA and Baylor University Medical Center, Dallas, Texas, USA
- Paras Patel, DDS - Center for Oral Pathology, Dallas, Texas, USA
- Victoria Woo, DDS - Department of Diagnostic Sciences, Texas A&M School of Dentistry, Dallas, Texas, USA
- Mehrnaz Tahmasbi Arashlow, DDS - Department of Diagnostic Sciences, Texas A&M School of Dentistry, Dallas, Texas, USA
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