Perkins Adiba, Desai Kurren, Trotter Bradley, Ward Russell, Sprowls Gregory, Zreik Riyam, Macmurdo Colleen, Tariske Lorelai, Birkemeier Krista
Texas A&M University, Temple, Texas, USA.
Department of Radiology, Baylor Scott & White McLane Children's Medical Center, Temple, Texas, USA.
Proc (Bayl Univ Med Cent). 2024 Sep 30;38(1):85-90. doi: 10.1080/08998280.2024.2403938. eCollection 2025.
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.
一名13岁男孩因左膝慢性间歇性疼痛和肿胀被转诊至骨科手术。初始影像学检查结果与股骨髁剥脱性骨软骨炎相符。后续影像学检查显示病情意外进展,有一个肿块延伸至髁间凹,取代了前交叉韧带,并侵蚀了股骨和胫骨髁。随后的手术活检和切除显示为肿瘤性钙化,最终诊断为常染色体隐性遗传性肿瘤性钙化。本病例报告强调了这种罕见疾病在这个不寻常部位的影像学表现、进展情况以及鉴别诊断。