Intra-articular nodular fasciitis: a rare lesion case report and an updated review of the literature
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Nodular fasciitis is a benign proliferation of myofibroblasts that usually arises in subcutaneous tissues of the trunk, neck, head, and upper extremities of young adults. It is not reported to arise in the joints.
In this report, we describe a rare case where nodular fasciitis occurred in an intra-articular location in the right knee of a 20-year-old man. The patient presented with 3-months’ duration of knee pain without history of trauma to the extremity. Physical examination revealed pain, joint effusion, and limited range of motion (ROM) of the affected knee. Magnetic resonance imaging (MRI) showed a 2.5 × 2 × 1 cm lesion in front of the posterior cruciate ligament. Arthroscopically, the soft tissue mass was removed and pathologically diagnosed as a rare, benign, intra-articular nodular fasciitis. Symptoms resolved 1 month after the operation and no recurrence was found at the 6 months follow-up.
The present paper describes detailed characteristics of intra-articular nodular fasciitis and provides an updated comprehensive summary of 21 prior case reports.
KeywordsIntra-articular nodular fasciitis Case report Updated review of the literature
giant cell tumour
no evidence of disease
non-steroidal anti-inflammatory drugs
pigmented villonodular synovitis
range of motion
smooth muscle actin
Nodular fasciitis is a benign myofibroblastic proliferation commonly found in young adults aged between 20 and 40 years [1, 2]. It usually arises in subcutaneous tissues of the trunk,  neck,  head,  and the upper extremities . Nodular fasciitis may also arise in the skeletal muscle,  dermis,  or in blood vessels,  although it is rarely reported within joints, leading to misdiagnosis. In addition to nodular fasciitis, knee pain may also arise from other diseases such as synovial chondromatosis, pigmented villonodular synovitis or giant cell tumour of the tendon sheath. We report a case of intra-articular nodular fasciitis in this study, and describe the clinical, radiological and pathological features of 21 previous case reports [10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21].
A 20-year-old man presented with a history of right knee pain of 3-months duration without any trauma or undue exercise. Physical examination showed joint effusion and limited range of motion. There was no locking in the joint and no palpable mass. He had no other significant past history.
Details of Antibodies Used in this Study
15E2E2 + 4C4.9
The symptoms of painful joint effusion and limited range of motion were improved 1 month after the operation. No recurrence was observed at the 6-months’ follow-up.
Clinical findings and radiological findings
Clinical and pathological features of cases of intraarticular nodular fasciitis
Clinical differential diagnoses included synovial chondromatosis (7 cases), pigmented villonodular synovitis (7 cases), giant cell tumour (4 cases), inflammatory arthritis (3 cases), complex ganglion (2 cases), lymphoma (1 case), gout (1 case), desmoid-type fibromatosis (1 case), low-grade myofibroblastic sarcoma (1 case), cartilage bodies (1 case), haemarthrosis (1 case), osteochondral fracture (1 case), malignant fibrous histiocytoma (1 case), haemangioma (1 case), lipomas (1 case), haemangiopericytomas (1 case), parosteal osteosarcomas (1 case), localized nodular synovitis (1 case), and fibromyxoid sarcomas (1 case). Three of 21 cases did not undergo arthroscopic surgery. The duration of follow-up ranged from 2 months to 86 months. No recurrence was observed.
Lesion sizes ranged from 1 to 6 cm (median, 3 cm) in the largest dimension. All tumours were a solid mass in gross appearance, usually grey or yellow.
Microscopic and immunohistochemical features
Histologic features showed typical nodular fasciitis, which was composed of cytologically bland and uniform plump spindle cells. The spindle cells were arranged within a variably loose myxoid to collagenous stroma in the form of short intersecting bundles. The loose myxoid to collagenous stroma contained scattered lymphocytes and red blood cells.
By immunohistochemistry, all cases showed that the spindle cells were diffusely positive for alpha-smooth muscle actin (SMA). All cases except one were negative for desmin. All cases except one were negative for caldesmon. None showed positive for nuclear beta-catenin and S-100 protein. One case in the shoulder showed positive for protein gene product (PGP) and negative for anaplastic lymphoma kinase 1 (ALK1) in the spindle cells. Another case in the shoulder showed negative for CD34 and CD68. Three cases in the knee showed positive for vimentin in the spindle cells. One case in the knee showed positive for muscle-specific actin, CD10 and negative for bcl-2 and cytokeratin AE1/AE3.
Only three cases, including one shoulder and two knees, did not undergo arthroscopic surgery to excise the lesion. Most patients’ symptoms were relieved a few days after surgery. For the patient with the lesion in the hip, partial weight-bearing on crutches and progressive post-operative mobilization were recommended, and the patient’s symptoms were relieved 3 weeks after surgery. Another case in the knee was recommended immobilization and non-steroidal anti- inflammatory drugs (NSAIDs) for 10 days, followed with physiotherapy with progressive mobilization; the patient’s symptoms were relieved 6 months after surgery. No recurrences were reported in any follow-up.
Intra-articular nodular fasciitis is rarely reported. Until now, only 21 cases of intra-articular nodular fasciitis have been documented in the literature (Table 2). To the best of our knowledge, only 1 previous clinicopathologic analysis of a series of intra-articular nodular fasciitis cases was reported, which only included 7 cases in knees, 2 cases in hands and 1 case in the ankle. In this present report, we described the case of intra-articular nodular fasciitis in the knee of a 20-year-old Chinese man and updated the case series of intra-articular nodular fasciitis, including 14 cases in knees, 3 cases in shoulders, 2 cases in hands, 1 case in the ankle and 1 case in the hip.
The clinicopathological features are summarized in Table 2. Most cases presented during the first to fifth decades of life, some with and some without trauma. The clinical history of patients with intra-articular nodular fasciitis is as short as 1 month. The lesions ranged from 1 to 6 cm. Radiologically, the lesions showed iso-signal intensity or lower signal intensity compared to muscle in T1-weighted and hyper-intensity T2-weighted MRIs. The follow up showed no recurrences, indicating it was a benign course.
It was usually misdiagnosed because of its rare incidence rate. Most cases were clinically misdiagnosed to be synovial chondromatosis (7 cases), pigmented villonodular synovitis (7 cases), giant cell tumour of tendon sheath (4 cases) or desmoid-type fibromatosis (1 case). These possibilities are excluded by histologic examinations. Histologically, the lesions showed typical nodular fasciitis, which is composed of cytological bland and uniform, plump spindle cells. The spindle cells were arranged within a variably loose myxoid to collagenous stroma in the form of short, intersecting bundles.
Desmoid-type fibromatosis is an abnormal growth that arises in the connective tissue, including abdominal wall, shoulders, upper arms, and upper legs . It is aggressive and can recur easily. Desmoid-type fibromatosis consists of sweeping fascicles of uniform, fibroblastic cells within a collagenous stroma. Blood vessels are often small and compressed in the lesion. Hyalinized or keloidal-type collagen fibres can usually be observed . Some studies indicated that nuclear beta-catenin by immunohistochemistry may be useful in differential diagnosis [22, 23, 24]. Additionally, the Ki67 proliferative index may also be useful for distinguishing nodular fasciitis from desmoids tumour .
Pigmented villonodular synovitis (PVNS, diffuse-type giant cell tumour) and giant cell tumour of tendon sheath (localized giant cell tumour of tendon sheath) were included in the giant cell tumours (GCT) of the synovium and tendon sheath . Histological examination reveals mononuclear stromal cell infiltrate involving synovial membrane, haemosiderin-laden macrophages, foam cells and multinucleated giant cells .
Synovial chondromatosis is determined by histological evaluation. The number of nodules in synovial chondromatosis can be counted in the thousands. Microscopically, the nodules are composed of hyaline cartilage with synovial tissue lining on the outside . The chondrocytes can show mild atypia, myxoid changes, calcification, or ossification .
Tendon sheath fibroma should also be distinguished from nodular fasciitis, because tendon sheath fibromas share most of the immunohistochemical markers with nodular fasciitis, such as positive vimentin, smooth muscle actin and negative desmin . However, tendon sheath fibroma is characterized by spindle-shaped and stellate-shaped fibroblasts, a fibrocollagenous, partly myxoid stroma, and slit-like vessels in histologic features . The presence of a less orderly, tissue culture-like growth pattern, extravasated red blood cells and more prominent myxoid stroma favours the diagnosis of nodular fasciitis .
Intra-articular fasciitis presented with some distinctive features from extra-articular fasciitis. On one hand, prominent stromal hyalinization is quite common in intra-articular lesions caused by repeated, frictional trauma. On the other hand, haemosiderin deposition is also frequently seen in tissues adjacent to intra-articular nodular fasciitis secondary to trauma.
Intra-articular nodular fasciitis, as in the musculoskeletal disorders, is usually identified with MRI. On the other hand, it was reported that ultrasound is also helpful in identifying the intra-articular nodular fasciitis . For musculoskeletal disorders, ultrasound is applied widely in evaluating dynapenia  and guiding subacromial corticosteroid injection .
In summary, nodular fasciitis can occur in the joints, most frequently in the knees and shoulders, without gender preference, in patients between 10 to 50 years old. It generally has a longer preoperative history than other cases of nodular fasciitis. The lesions show iso-signal or lower intensity compared to muscle in T1-weighted and hyper-intensity T2-weighted MRIs. The histological features are typical of nodular fasciitis, consist of a bland fibroblastic proliferation arranged in irregular fasciitis with tissue-culture-like appearance. It appears not to recur, though the number of reported cases is limited. Awareness of the occurrence of nodular fasciitis within joints including knees, shoulders, hands, ankle and hip will lead to the correct diagnosis. Additional reports about intra-articular nodular fasciitis cases in the elbow and other joints are needed in the future.
The authors thank the following pathologists and surgeons who kindly provided help: Dr. Nelson, Scott D., MD, UCLA, USA; Dr. Weigang Wu, Zhejiang University, China; Dr. Zhimin Ying, Zhejiang University, China; Dr. Xiaobo Yan, Zhejiang University, China; and Dr. Xiang Zhao, Zhejiang University, China.
This study was funded by Zhejiang Province Natural Science Foundation (NO. LQ18H060001), Zhejiang Province Medical and Health project (NO. 2018269731), Zhejiang Province Chinese Medicine Project (NO. 2015ZB028) and National Natural Science Foundation of China(NO. 81602312). The funding played role in collecting the case, buying the literatures of nodular fasciitis and analyzing the features of nodular fasciitis.
Availability of data and materials
The public can get the raw data from the author by email of Shigui Yan.
WW and YTH wrote the draft of the manuscript and participated in the follow-up examination of the patient and clinical material. CXW read the pathological results and prepared the figures. JQH, CYM and HBW participated in the surgical and medical treatment and followed up the patient. NL and ZMY, the orthopedics surgeons, took part in the operation of this case and were involved in drafting the manuscript and revising it. SGY performed the surgery, coordinated and helped to draft and finalize the manuscript. All authors read and approved the final manuscript.
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The authors have obtained the patient’s written informed consent for print and electronic publication of this case report.
The authors declare that they have no competing interest.
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