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Fibroma of tendon sheath in planta
SpringerPlus volume 5, Article number: 575 (2016)
Fibroma of tendon sheath in planta is comparatively rare, and its differentiate diagnose, tumour features, treatment and complications were lack of retrospective study in clinics.
This was a retrospective study of 13 patients (seven women, six men) operated between July 2001 and May 2013 for FTS in planta. The average age at the time of the procedure was 49.8 ± 8.3 years old (range 31–64). The female-to-male ratio was 9:4. Before the surgery, anteroposterior, lateral and oblique position of foot X-rays were performed in all patients. Ultrasonography (n = 11) and magnetic resonance imaging (n = 11) were performed selectively. The tumor located on the metatarsal par (n = 6), the central part of plantar (n = 4), the lateral part (n = 2) and the medial part (n = 1). Eight patients presented with painless mass (62 % of cases), while five patients presented with pain mass (38 % of cases). No patient had bony erosion. This paper studies the different features of FTS and classifies them into two types—superficial type that tumour grows at planter fascia; deep type that breaks through the planter fascia growing around tendon and joint capsule. Eight and five patients were diagnosed as superficial type and deep type respectively.
In all cases, the tumor was excised, pathological results was FTS. The mean follow-up period was 3.2 ± 1.1 years (range 2–7) years. Five patients had neurovascular bundle involvement (38 % of cases). Two patients had a recurrence (15 % of cases), they undergone another operation. Four patients had a pain (31 % of cases), two patients had numbness (15 % of cases), and one patient had pain and numbness (8 % of cases). They recovered after conservative treatment.
For the FTS that grows in the plantar, we should select differential diagnosis and the corresponding therapy according to the features of two types, also the prognosis is different.
Level of evidence
In 1936, Gechickter and Copeland (Chung and Enzinger 1979) first described a benign soft tissue lesion as FTS. FTS typically shows a small, well-circumscribed subcutaneous tumour. FTS can occur at any age, with a peak incidence at 20–50 years of age (Chung and Enzinger 1979). Chung and Enzinger (1979) reported 138 cases, in their series, 98 % of the lesions were in the extremities, and 82 % were in the upper extremities. Five cases occurred in the foot, and four of them demonstrated that the tumor was located in the plantar region. Excision has been the treatment of choice. FTS originates in the tendon or tendon sheath (Chung and Enzinger 1979; Fox et al. 2003). A high incidence of local recurrence, ranging from 11 to 25 % has previously been reported (Chung and Enzinger 1979; Humphreys et al. 1986). FTS in planta is comparatively rare, can be hard to distinguish from other lesions, only isolated case reports in previous literature. We report its clinical presentation, differentiate diagnose, treatment, tumour features and outcome in a retrospective study,which can be used to guide treatment in clinic.
Patients and methods
From the First Affiliated Hospital, College of Medicine, Zhejiang University. This was a retrospective study with 13 patients (seven women, six men) presenting with a FTS in planta and operated between July 2001 and May 2013. Ethical approval was given by the medical ethics committee of the First Affiliated Hospital, College of Medicine, Zhejiang University. The average age was 49.8 ± 8.3 years (range 31–64). All the patients presented with gradually progressive swelling mass. Eight patients presented with painless mass (62 % of cases), while five patients presented with pain (38 % of cases). An injury to the area had preceded the appearance of the lesion (n = 4). Before the operations, anteroposterior, lateral and oblique position of foot X-rays were performed in all patients. Ultrasonography (n = 11) and magnetic resonance imaging (MRI) (n = 11) were performed selectively. The lesions were located on the metatarsal par (n = 6), the central part of plantar (n = 4), the lateral part (n = 2) and the medial part (n = 1) (Table 1). No patient had multiple lesions. All patients received fine needle biopsy. According to the different locations and features of tumours, we try to divides the tumours into two types (Table 2)—superficial type that the mass grows at planter fascia, and deep type that breaks through the planter fascia and grows around tendon and joint capsule. All patients underwent surgery to remove the tumour by an independent Surgeon. The surgical procedure was performed under regional or general anesthesia. A brachial tourniquet was used systematically and the procedure was carried out with surgical loupes. After the surgery, the drainage tube needed placing and no antibiotics would be used. All patients were able to walk with load under the protection of braces when the incision had healed. All patients would be evaluated again by an independent Surgeon. A clinical questionnaire was completed over the telephone and at the clinic. All the patients had been interviewed and completed regular follow-up visits. The clinical and radiographic examinations would be performed regularly in the follow-up study. Three patients (23 % of cases) were undergone the rechecks of X-ray, Ultrasonography and MRI were used as a tumor recurrence standard.
Pathological results confirmed it as FTS, which composed of tightly packed spindle cells surrounded by collagen fibers. The mean follow-up period was 3.2 ± 1.1 years (range 2–7). No patient had bony erosion. Eight and five patients were diagnosed as superficial type and deep type respectively. Five patients had neurovascular bundle involvement (38 % of cases) with decompression in operation. Clinical suspicion of neurovascular bundle involvement arose when the patients presented with pricking or irradiated pain. Complications have been recorded including tumour recurrence pain and numbness. Two patients had a recurrence (15 % of cases), they undergone reoperation. Four patients had a pain (31 % of cases), two patients had numbness (15 % of cases), and one patients had pain and numbness (8 % of cases). Conservative management with Neurotrophy medicine and NSIAD were appropriate for those patients.
The diagnosis of FTS is supposed to be confirmed by several aspects such as the patient’s history, the clinical examination, and radiologic and pathologic findings. The major differential diagnosis of superficial type of FTS (Fig. 1) includes plantar fasciitis, plantar fascial fibromatosis and nodular fasciitis. Plantar fasciitis occurs because the supporting plantar fascia of the arch becomes strained and inflamed. The prevalence of plantar fasciitis in the general population is estimated to range from 3.6 to 7 % (Dunn et al. 2004; Hill et al. 2008), is a common problem that affects sport participants as well as inactive middle-aged individuals (Davis et al. 1994; Martin et al. 1998). The patients diagnosed as the superficial type had trauma history commonly. Even if some of them did not have trauma history, the tumor occurring resulted from surface of planta was rubbed frequently. Plantar fascial fibromatosis (Bedogni and Dal Monte 1962; Koudela et al. 2010; Dartoy et al. 1990), also known as Ledderhose’s disease, is a relatively uncommon non-malignant thickening of the feet’s deep connective fascia. At the beginning of the disease, cords and nodules start growing along the plantar fascia. Therefore, that is easy to be confused with FTS. The nodules are slowly growing, most of them are often found in the central and medial portions of the plantar fascia. And at the end of the disease, the cords thicken, the toes stiffen and bend (Barnes et al. 2009). However, the FTS on the surface of plantar cannot influence on the toes. Nodular fasciitis is a benign, fibroproliferative lesion that is thought to represent a reaction to injury or inflammation (Cotter et al. 2000). It most frequently affects the upper extremities, especially the volar aspect of the forearm (Brown and Carty 2005). The characteristic vascular pattern of FTS is not seen in nodular fasciitis microscopically (Hornick and Fletcher 2006). Pathologic examination is the gold standard for diagnosis of FTS, sometimes diagnosis requires immunohistochemical confirmation. Deep type of FTS (Fig. 2) should be differentiated from giant cell tumor of the tendon sheath (GCTTS). These two lesions are similar in size, location, and gross appearance. GCTTS mostly occurs in the toes (Gibbons et al. 2002; Darwish and Haddad 2008). Satti (1992) suggested the pathological study between FTS and GCTTS is difficult to identify. GCTTS may present with bone erosion or destruction in radiography (Uriburu and Levy 1998; Lu et al. 2015). There were infrequent above imaging features in FTS. And there were no giant cells in FTS observed under microscope.
Both Ultrasound and MRI are options for FTS. We choose ultrasound for superficial type of FTS. Ultrasound is an important way with its advantage of noninvasive convenience, also making a more definite diagnosis. Solid soft tissue tumors may be confused with cystic masses on ultrasonography (Lee et al. 2010), so we suggest that using MRI as an additional screening tool. Normally, FTS has a lower signal or slightly higher intensity signal on T2-weighted images. But due to the edema in the tumour or capillary vascularity surrounding tumour reacts high intensity signal on T2-weighted images (Fox et al. 2003). Deep type of FTS especially when neurovascular was involved, MRI play an important role in studying the anatomy, and avoid nerves damage during surgery. The images of tendon and tendon sheath provided effective information for resection range and selecting the most reasonable incision. MRI also would help the clinician finding early recurrence more effectively.
The treatment of FTS is surgical resection. FTS is excised together with the overlying tendon sheath. The indication for surgery is aches and pain. But patients had FTS without any painful discomfort initially also need early resection. Excise to relieve symptoms but preserve function, may be difficult to remove from adherent tendons. Preoperative diagnosis and type are helpful for the design of the operation planning. Superficial type of FTS was easier to remove. But deep type of FTS grows around tendon and joint capsule, especially some patients had neurovascular bundle involved, is difficult to remove from adherent tendons. The tumor cannot be excised completely, which is the main reason to have a recurrence after the surgery. The nerve injury should be avoided during operation. Nerve injury during operation could lead to numbness. Painful scar is also a difficult problem. Light therapy and lasers are meant to minimize its appearance. A malignant transformation has never been described. Only tumour recurrence needs reoperation in follow-up.
According to the different types of FTS growing in planta, the prognosis is different. Preoperative definite type is helpful for the design of the operation plan. The deep type commonly has adhesion to the neurovascular bundle. It is difficult to excise completely, has a high recurrence after surgery as well as easy to produce complications of numbness and pain. MRI is developed in an attempt to minimize surgical damage and preserve nerves function.
fibroma of tendon sheath
giant cell tumor of the tendon sheath
magnetic resonance imaging
Barnes DE, Adedapo A, Allison K (2009) The treatment of severe flexion contracture of the great toe in a patient with Ledderhose’s disease. J Plast Reconstr Aesthet Surg 62(1):102–104. doi:10.1016/j.bjps.2007.08.004
Bedogni C, Dal Monte A (1962) Plantar fibromatosis (Ledderhose’s disease). La Chirurgia degli organi di movimento 51:25–38
Brown V, Carty NJ (2005) A case of nodular fascitis of the breast and review of the literature. Breast 14(5):384–387. doi:10.1016/j.breast.2004.09.014
Chung EB, Enzinger FM (1979) Fibroma of tendon sheath. Cancer 44(5):1945–1954
Cotter CJ, Finn S, Ryan P, Sleeman D (2000) Nodular fascitis of the maxilla in a child. J Oral Maxillofac Surg 58(12):1447–1449. doi:10.1053/joms.2000.16642
Dartoy C, Le Nen D, Riot O, Lefevre C, Courtois B (1990) Ledderhose’s disease. Report of 7 cases. J Chir 127(11):533–536
Darwish FM, Haddad WH (2008) Giant cell tumour of tendon sheath: experience with 52 cases. Singap Med J 49(11):879–882
Davis PF, Severud E, Baxter DE (1994) Painful heel syndrome: results of nonoperative treatment. Foot Ankle Int 15(10):531–535
Dunn JE, Link CL, Felson DT, Crincoli MG, Keysor JJ, McKinlay JB (2004) Prevalence of foot and ankle conditions in a multiethnic community sample of older adults. Am J Epidemiol 159(5):491–498
Fox MG, Kransdorf MJ, Bancroft LW, Peterson JJ, Flemming DJ (2003) MR imaging of fibroma of the tendon sheath. AJR Am J Roentgenol 180(5):1449–1453. doi:10.2214/ajr.180.5.1801449
Gibbons CL, Khwaja HA, Cole AS, Cooke PH, Athanasou NA (2002) Giant-cell tumour of the tendon sheath in the foot and ankle. J Bone Joint Surg Brit 84(7):1000–1003
Hill CL, Gill TK, Menz HB, Taylor AW (2008) Prevalence and correlates of foot pain in a population-based study: the North West Adelaide health study. J Foot and Ankle Res 1(1):2. doi:10.1186/1757-1146-1-2
Hornick JL, Fletcher CD (2006) Intraarticular nodular fasciitis—a rare lesion: clinicopathologic analysis of a series. Am J Surg Pathol 30(2):237–241
Humphreys S, McKee PH, Fletcher CD (1986) Fibroma of tendon sheath: a clinicopathologic study. J Cutan Pathol 13(5):331–338
Koudela K Jr, Koudela K Sr, Kunesova M, Koudelova J (2010) Plantar fibromatosis (Ledderhose’s disease). Acta chirurgiae orthopaedicae et traumatologiae Cechoslovaca 77(4):341–345
Lee MH, Kim NR, Ryu JA (2010) Cyst-like solid tumors of the musculoskeletal system: an analysis of ultrasound findings. Skelet Radiol 39(10):981–986. doi:10.1007/s00256-010-0902-8
Lu H, Shen H, Chen Q, Shen XQ, Wu SC (2015) Artificial finger joint replacement due to a giant cell tumor of the tendon sheath with bone destruction: a case report. Oncol Lett 10(6):3502–3504. doi:10.3892/ol.2015.3813
Martin RL, Irrgang JJ, Conti SF (1998) Outcome study of subjects with insertional plantar fasciitis. Foot Ankle Int 19(12):803–811
Satti MB (1992) Tendon sheath tumours: a pathological study of the relationship between giant cell tumour and fibroma of tendon sheath. Histopathology 20(3):213–220
Uriburu IJ, Levy VD (1998) Intraosseous growth of giant cell tumors of the tendon sheath (localized nodular tenosynovitis) of the digits: report of 15 cases. J Hand Surg 23(4):732–736. doi:10.1016/S0363-5023(98)80062-2
HL, QC and HS performed the data collection. XS and SW designed the study and performed the analysis. HL drafted the manuscript. All authors read and approved the final manuscript.
First and foremost, I would like to show my deepest gratitude to my colleagues Dr. Qiang Chen, Dr. Hui Shen, Dr. Xiang-qian Shen, Dr. Shou-cheng Wu, who have provided me with valuable assist in every stage of writing this paper. Meanwhile, I also appreciate Zhejiang traditional Chinese medicine Research Program for sponsoring our research (the Grant No. 2016ZA124). Last but not least, I’d like to thank all my friends, especially my lovely wife for her translation, encouragement and support.
The authors declare that they have no competing interests.
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Lu, H., Chen, Q., Shen, H. et al. Fibroma of tendon sheath in planta. SpringerPlus 5, 575 (2016) doi:10.1186/s40064-016-2260-z
- Fibroma of tendon sheath
- Neurovascular bundle involvement