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Hypertrophic pulmonary osteoarthropathy in bilateral distal tibia and fibula
Fumihiro Inoue1, Masanori Taki2, Kazunari Oshima2
1Departments of Foot and Ankle Surgery, Seirei Hamamatsu Hospital, Hamamatsu, Shizuoka Prefecture, Japan fm23fm23.63@gmail.com.
Abstract:
Hypertrophic pulmonary osteoarthropathy (HPOA) is a rare syndrome involving periosteal new bone formation, joint pain and digital clubbing, commonly secondary to pulmonary disease. It is frequently misdiagnosed as a primary orthopaedic disorder, which may delay appropriate systemic evaluation. A man in his late 60s with bilateral ankle pain visited our outpatient foot and ankle clinic. Radiographs and CT scans revealed symmetric periosteal new bone formation in both tibiae and fibulae. MRI showed no bone marrow abnormalities, supporting the diagnosis of HPOA. Further investigation revealed a lung tumour; the patient's symptoms significantly improved following lobectomy. The differential diagnosis of periosteal new bone formation in the lower extremities includes various conditions. The absence of bone marrow lesions on MRI and the bilateral, symmetric distribution of changes are key diagnostic clues for HPOA.
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The first classification is based on the development of the disease, and it includes the following categories: