A 30-year-old man had 2½ years of painful swelling involving his right ring finger proximal inter-phalangeal joint (PIPJ) with restricted movement. There was no preceding injury, no exposure to tuberculosis (TB) or other medical history. There was, however, family exposure to TB. Some relief obtained with non-steroidal anti-inflammatory drugs (NSAIDS).
Initial X-ray showed PIPJ soft tissue swelling, no erosive change or focal bone lesion. Initial MRI showed peri-articular soft tissue/bone marrow oedema with small PIPJ joint effusion & no soft tissue tumour. Initial diagnosis was dactylitis/TB inflammatory mono-arthropathy. Initial synovial biopsy showed no evidence of malignancy, TB or sarcoid granuloma. Oral steroids gave minimal relief. Ultrasound guided steroid injection gave minor relief. There was significant synovitis and hypervascularity on pre-injection images.
Repeat MRI was similar to first MRI; bone marrow oedema at proximal phalanx/PIPJ with moderate tenosynovitis. Second synovial biopsy showed non-specific inflammation and no granuloma.
After PIPJ fusion using crossed K-wires, histology of localized bone curettage confirmed osteoid osteoma. The patient has been asymptomatic for 1 year since fusion.
CT examination post fusion showed satisfactory position of wires with no evidence of any features of osteoid osteoma (previously discussed).
Final X-ray after K-wire removal showed satisfactory evidence of healing post fusion.
Osteoid osteomas are benign bone tumours of growing skeletons. [1] They constitute about 10% of benign bone neoplasms with classic symptoms of intermittent worsening pain mainly at night. 8% osteoid osteomas occur in order of decreasing incidence in the hand, phalanges, carpals and metacarpals.
Diagnosis is tricky with variable features on imaging.
[2] Plain films show classic small ovoid radiolucent lesions with surrounding sclerosis, also seen on CT. MRI shows prominent oedema with low/intermediate signal focus on T1 sequences indicating the nidus.
[3] Intra-articular lesions cause non-specific symptoms such as synovitis, decreased range of movement, joint effusion and lack of a focal sclerotic lesion on radiographs. In one series, 9 intra-articular lesions were shown in the hip, elbow, ankle and meta-tarsals.
[4] Osteoid osteomas in phalanges of the hand in another series describe absence of reactive bone, mono-articular arthritis, clubbing, macrodactyly, painless swelling and absence of bony lysis.
[5] Another series of 48 upper limb osteoid osteomas, 5 were in proximal phalanges, 4 were in distal phalanges. Radiographs were sufficient for diagnosis in 32/48. 16/48 with no X-ray evidence had a hot spot on bone scan.
This case highlighted diagnostic difficulties. The only typical feature in history was minor relief with NSAIDS. The overwhelming history, imaging (USS/MRI) pointed to an inflammatory mono-arthropathy with response to intra-articular steroid and two synovial biopsies excluding sarcoid and TB.
The imaging features were atypical. The X-ray showed soft tissue swelling suggestive of mono-articular arthritis. There was no evidence of reactive bone sclerosis or lysis. MRI showed bone marrow oedema on both sides of the PIPJ, but more prominent on the proximal side. There was a joint effusion and tenosynovitis pointing to an inflammatory arthropathy. With retrospect the only feature to suggest a potential nidus was a 1-2mm low signal focus on MRI centrally in the marrow oedema, (only visualized on perhaps 2 images in different planes), adjacent to the articular surface of the proximal phalanx at the PIPJ. Ultrasound confirmed hypervascularity with a joint effusion/tenosynovitis.
CT examination post fusion did not show evidence of potential nidus or sclerosis adjacent to the crossed K-wires. The post-removal X-ray showed satisfactory healing. If the nidus is removed, the patient should be asymptomatic for a significant time period.
This was an unusual presentation of intra-articular phalangeal osteoid osteoma with non-specific history/imaging features and initial histology. The intra-articular nature of the lesion, the lack of conclusive imaging features and previous histology and more common diagnoses in the differential made the diagnosis difficult.
Intra-articular osteoid osteoma in proximal phalanx.
Based on the X-ray, MRI, ultrasound, and CT images of the patient’s right hand fourth finger (ring finger) proximal interphalangeal joint (PIPJ), the main observations are as follows:
Overall, the imaging features are atypical: there is a lack of obvious sclerotic changes or the classic “nidus” structure often associated with osteoid osteomas across various imaging modalities. On MRI, only a tiny (1–2 mm) low signal area is suggestive, accompanied by joint effusion and synovitis, leading to diagnostic challenges.
Based on the patient’s history (2.5 years of persistent pain and swelling, partially relieved by NSAIDs), imaging features, and repeated exclusions of infection and inflammatory joint diseases, the following differential diagnoses are considered:
Considering the patient’s age, clinical symptoms (joint pain, partial response to NSAIDs), local joint swelling, and imaging (only a vague tiny low-signal lesion on MRI, with bone marrow edema and synovitis, and no evidence of typical infection or rheumatic markers), the most likely diagnosis is:
This condition is relatively rare and can be easily delayed in diagnosis. Intra-articular lesions often lack the typical reactive sclerosis and can mimic arthritis or synovitis. For precise localization or confirmation, a high-resolution CT scan or a targeted biopsy during symptomatic periods may be considered.
If osteoid osteoma is confirmed or highly suspected, the following treatment strategies and subsequent rehabilitation plans may be considered:
Throughout rehabilitation, exercise intensity and range of motion should be individualized based on the patient’s age, bone quality, overall health status (especially any cardiovascular or chronic conditions), ensuring safety and comfort.
This report is provided as a reference based on the available imaging and clinical information. It does not replace an in-person consultation or professional medical advice. Actual diagnosis and treatment must be determined by qualified medical professionals after reviewing the patient’s full medical history, physical examination, laboratory tests, and other diagnostic findings.
Intra-articular osteoid osteoma in proximal phalanx.