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. 2021 Nov 19;118(46):781–788. doi: 10.3238/arztebl.m2021.0325

Dupuytren’s Disease—Etiology and Treatment

Mike Ruettermann 1,2,3,*, Robert Michael Hermann 4, Karl Khatib-Chahidi 5, Paul MN Werker 2
PMCID: PMC8864671  PMID: 34702442

Abstract

Background

The worldwide prevalence of Dupuytren’s disease (DD) is 8%. DD is a chronic disease for which there is no cure. Various treatments are available.

Methods

This review is based on pertinent publications retrieved by a selective search in PubMed and Embase.

Results

Genetic factors account for 80% of the factors involved in causing this disease. Diabetes mellitus, hepatic diseases, epilepsy, and chronic occupational use of vibrating tools are also associated with it. Limited fasciectomy is the most common treatment and is considered the reference standard. Possible complications include persistent numbness in areas where the skin has been elevated, cold sensitivity, and stiffness, with a cumulative risk of 3.6 –39.1% for all complications taken together. The recurrence rate at 5 years is 12–73%. Percutaneous needle fasciotomy is the least invasive method, with more rapid recovery and a lower complication rate than with limited fasciectomy. 85% of patients have a recurrence after an average of 2.3 years. Radiotherapy can be given before contractures arise in patients with high familial risk, or postoperatively in selected patients with a very high individual risk of recurrence.

Conclusion

Although DD is not curable, good treatments are available. Recurrences reflect the pathophysiology of the disease and should not be considered complications of treatment. When counseling patients about the available treatment options, particularly the modalities and timing of surgery, the physician must take the patient’s degree of suffering into account. Nowadays, fast recovery from surgery and less postoperative pain are a priority for many patients. Different surgical methods can be used in combination. It remains difficult to predict the natural course and the time to postoperative recurrence in individual patients; these matters should be addressed in future studies.


cme plus

This article has been certified by the North Rhine Academy for Continuing Medical Education. Participation in the CME certification program is possible at cme.aerzteblatt.de. The deadline for submission is 18 November 2022.

Dupuytren’s disease is characterized by progressive idiopathic fibrosis of the palmar aponeuroses of the hands, leading to extension deficit in the fingers and the formation of nodules. Its course can vary greatly between individuals. The staging is shown in Table 1.

Table 1. Staging of Dupuytren’s disease.

Stage Tubiana*: Total extension deficit of all joints in the most affected finger Meyerding Iselin
0 No fibrosis or extension deficit
N Fibrosis, no extension deficit
N/1 Fibrosis, extension deficit up to 10°
1 Fibrosis, extension deficit up to 45° Fibrosis without functional impairment Fibrosis in the palm without extension impairment
2 Fibrosis, extension deficit 45°– 90° Fibrosis with mild contracture in the MCP joint Fibrosis with contracture in the MCP joint
3 Fibrosis, extension deficit 90°– 135° Fibrosis in the PIP joint, contractures in the MCP and PIP joints Fibrosis with contracture in the MCP and PIP joints
4 Fibrosis, extension deficit greater than 135° Hyperextension contracture of the DIP joint Fibrosis with advanced contracture in the MCP and PIP joints and hyperextension of the DIP joint

* In the Tubiana classification, some lesions can be characterized more precisely by the use of single-letter abbreviations as follows:

N, nodule or cord in the palm without flexion contracture; P, lesion mainly localized in the palm; D, lesion mainly localized on the finger

Dupuytren’s disease is a chronic disease and cannot be cured by surgery. Surgical resection may be followed by a remission that lasts for years or by early recurrence. The causes of early recurrence remain disputed. Hueston introduced the concept of diathesis (1). Factors such as a positive family history, bilateral disease, age at onset below 50 years, the presence of concomitant diseases such as Ledderhose’s disease (idiopathic fibrosis of the plantar aponeurosis), Peyronie’s disease (induratio penis plastica), and Garrod’s pads (“knuckle pads” or “Garrod’s nodules”) are predictors of recurrence. The histology of resected tissue can also indicate a high risk of recurrence, e.g., if the fibrotic tissue shows high cellularity and mitosis (Rombouts type 1) (2, 3).

Prevalence and incidence

A recent meta-analysis calculated a worldwide prevalence of approximately 8% (4). The highest reported prevalence rates are 17% in Africa, 15% in Asia, 10% in Europe, and 2% in the Americas. Men are 3 to 4 times more likely to be affected than women, and the incidence per 10 000 head of population increases with age, rising from approximately 5 in the age group below 50 years to 15 (50–59 years), 30 (60–69 years), and finally 40 (70–79 years) (4, 5).

Etiology and risk factors

Complex genetic analyses carried out by Ng and others showed no evidence to support the previously postulated theory associating Dupuytren’s disease with Nordic or “Viking” ancestry (68).

It is now known that Dupuytren’s disease is caused by interactions between multiple genes that are expressed variably and in a delayed manner. The Genome-Wide Association Study (GWAS) identified 26 genomic regions associated with Dupuytren’s disease (6, 9), and this is probably just the tip of a genetic iceberg (9). A cohort study of over 30 000 Danish pairs of twins showed that the heritability of Dupuytren’s disease is around 80% (10). Among 730 men with Dupuytren’s disease, the prevalence of plantar fibromatosis (Ledderhose’s disease) was 16% (plastic surgeons’ assessment) or 22% (patients’ assessment). The prevalence of induratio penis plastica (Peyronie’s disease) was assessed at 7.8% and 8.8%, respectively (11).

Additional associations exist with particular diseases such as diabetes mellitus (types 1 and 2) (odds ratio [OR] 3.06, 95% confidence interval [2.69; 3.48]), liver disease (OR 2.92 [2.08; 4.12]), and epilepsy (OR 2.80 [2.49; 3.15]); no specific form of epilepsy or anticonvulsant medication has been identified (12). Other factors that can be influenced by lifestyle changes appear also to play a role in the expression of the phenotype (13). Increased alcohol consumption is associated with an OR of 1.71 [1.25; 2.33] (14).

Working with vibrating tools for many (>15) years (“vibration exposure”) is also significantly associated with Dupuytren’s disease, with an OR of 2.87 [1.41; 5.84] according to a recent meta-analysis (15, 16). Age, too, seems to be of relevance: a cohort study of 23 795 persons showed a clear association between Dupuytren’s disease and manual labor for those younger than 60 years (adjusted OR 2.08 [1.03; 4.2]), but not for those over the age of 60 (17). Further studies are needed to determine the exact connection between vibration and Dupuytren’s disease. However, the existing evidence is robust enough for patients to be informed of these findings to help guide their decision making in relation to both work and leisure.

Anatomy of the fascia of the hand and fingers

In recent years, microanatomical dissections prompted by discordances between previously familiar anatomical descriptions and intraoperative findings have shed new light on the anatomy distal to the transverse ligament of the palmar aponeurosis (18). These new findings are clinically significant and must be taken into account when options for surgical treatment are being considered. Details are given in the eBox. When affected by Dupuytren’s disease, the course of the palmodigital spiral system results in a spiral course of the digital nerves, which can lead to intraoperative nerve injury (1921) (figure 1).

eBOX. Fascial anatomy of the hand and fingers.

In recent years, microanatomic dissections carried out because of discordances between previously known anatomical descriptions and intraoperative findings have shed light on the anatomy of the palm of the hand distal to the transverse ligament of the palmar aponeurosis (TLPA) (e16). These new findings are of clinical importance and must be taken into account when surgical treatment options are being considered.

It had long been assumed that the middle layer of pretendinous fibers (McGrouther layer 2) passes beneath the neurovascular bundle and the natatory ligament (NL) to merge with the lateral digital sheet (LDS) in the proximal phalanx. However, microanatomic preparations revealed an anatomical structure that was named the “palmodigital spiral system” (PSS). The course followed by this structure as it spans the palmar and digital fibers is different from that previously described. Proximally, this PSS also fuses with fibers of the intrinsic muscle fasciae. All these proximal fibers insert on the dorsal aspect of the NL, so that the pretendinous layer 2 fibers actually course in a 360° spiral. The course of these fibers can result in a spiral course of the neurovascular bundle in this area, thus increasing the risk of intraoperative nerve injury. Because of the insertion of these fibers on the underside of the NL in this region the spiral course of the nerve begins proximal to the NL. The presence of fat between the skin and the cord is pathognomonic of displacement of the neurovascular bundle in this region (e17). If the fibers of the intrinsic muscle fasciae are also diseased and cause a contracture spanning the MCP joint, treatment by percutaneous needle fasciotomy (PNF) or collagenase becomes difficult since this cord cannot be reached without potentially damaging the neurovascular bundle.

Fibers originating from the proximal annular ligament form the middle part of the PSS. These fibers spiral up to 180° and course across the lateral digital sheet into the best developed part of Grayson’s ligament, which covers the palmar aspect of the neurovascular bundle. They also fuse with Cleland’s ligaments, which partly originate on the side of the tendon sheath (e18, e19). Because of these connections, pathological changes can result in the digital nerve coursing in a second spiral in the area of the proximal phalanx (e20).

Another clinically important finding is convergence of the proximal fibers of the PSS with those of the adjacent finger just distal to the bifurcation of the common digital artery. This explains why some cords appear to cross from one ray to the next, forming so-called Y-cords. Precise knowledge of this complex three-dimensional microanatomy of the structures involved in Dupuytren’s disease is important for hand surgery.

Figure 1.

Figure 1

Intraoperative photograph of recurrent Dupuytren’s disease in the left little finger, showing

a) spiral course of the radial digital nerve; b) here this spiral nerve is marked with yellow dots; the normal anatomical course of the radial digital nerve is shown in green.

Surgery

Although the resections are performed in the area of the palmar aponeurosis, the surgical procedures have become known by the term “fasciectomy.”

Once it emerged in the 1960s that radical fasciectomy (RF), by which surgeons had hoped to prevent recurrence by removing all the fascial tissue, was not only noncurative but also morbidity-prone (22), less radical resections were introduced, such as limited fasciectomy (LF, with various incisions) or segmental fasciectomy (SF), in which only 1-cm segments of the pathological cords are removed (23). The most recently introduced procedures are minimally invasive: percutaneous needle fasciotomy (PNF) and injections of collagenase obtained from Clostridium histolyticum (CCH).

There is still a lack of high-quality studies comparing several different options for treatment (24, 25). Randomized controlled trials between single techniques have been carried out and are described below.

At present, limited fasciectomy (LF) remains the commonest treatment for Dupuytren’s disease (23) and may be considered the reference standard. Its popularity is due to several reasons. Ultimately, most patients are satisfied with the outcome, since the hands operated on mostly regain good function. Wound healing and scar maturation often take a long time, interfering with daily work and leisure activities, but nevertheless, patients generally accept the inconvenience because of the satisfactory esthetic improvement (26).

Possible complications include persistent numbness in areas where the skin has been lifted, sensitivity to cold, and stiffness, with a cumulative risk of 3.6%–39.1%; in terms of serious complications such as nerve injury or the like, the cumulative risk is 15.7% (27). The recurrence rate at 5 years ranges from 12% to 73%, and early recurrences also occur despite surgery (28). Some patients are so disappointed by this that they refuse further surgical intervention and accept their limited finger extension.

Less invasive techniques are associated with a significantly shorter recovery time and therefore deserve a place in the repertoire of every hand surgeon.

We therefore describe the alternatives to LF in terms of ability to straighten the fingers (efficacy), patient-reported outcome measures (PROMs), complications, duration of wound healing, and durability of the outcome.

With segmental fasciectomy (SF), the reported overall complication rate is lower, with a cumulative risk of 0–5.6%, although the reporting in the available studies is of poorer quality. The advantages of SF are mainly faster recovery with less postoperative pain (29, 30). Whether incomplete resection of the cord is associated with a higher risk of recurrence than after LF has not been investigated in high-quality comparative studies. Available cohort studies (Oxford level of evidence 2b) have not yet provided any evidence for this, nor any regarding long-term outcomes, although control groups are lacking (2931).

Percutaneous needle fasciotomy (PNF) is the least invasive surgical procedure. High-quality studies (Oxford level of evidence 1b) over the past 15 years show that for contractures up to 90° PNF has a similar efficacy to LF. However, recovery is much faster, with a lower complication rate of 0% for PNF compared with 5% for LF (3235). The disadvantage of PNF is the shorter time to progression/recurrence (85% recurrence after a mean of 2.3 years) compared with LF (23.8% recurrence after a mean of 3.7 years) (34). However, this is usually not a problem, as the treatment can be repeated to similar good effect without increasing the risk of complications. In addition, LF can usually be performed as safely after PNF as when it is performed as the primary procedure (36, 37). However, if the cords are wider (“logs” versus “twigs” [38]), the possibility that an extension deficit can be corrected by PNF seems limited. Even so, PNF may be performed by skilfull hands. For example, in safe locations (for example, the palm) a thicker needle can be used to release the skin from fibrosis in the horizontal plane, reducing the risk of skin tears. Even when PNF is performed “blind” there is no need, if it is done correctly, to anticipate an increased risk of injury to vessels or nerves (39). The cost of PNF is significantly lower than that of any other surgical treatment for Dupuytren’s disease (40).

Chemical cleavage by injection of collagenase has been discontinued almost everywhere because of the cost of the drug relative to its effectiveness and the recurrence rate. Its efficacy proved to be comparable to that of PNF. The efficacy has been studied in several randomized controlled trials, and the longer the follow-up, the more similar the recurrence rates became. After three years, recurrence rates were identical, with a remaining total extension deficit of 15° after PNF and 28° after collagenase injection (P = 0.05) (e1e3). Collagenase injection is indicated, for example, in patients with recurrence after multiple LF with wide cords (“logs” versus “twigs”) (38), or in already neurovascularly compromised fingers with a functionally limiting extension deficit. However, the drug would have to be ordered from abroad as it is not available in Germany.

The most radical treatment is dermofasciectomy (DF) with skin grafting, which may be considered as the last resort in patients with recurrences after LF or those with severe primary disease (e4, e5). This procedure involves removal of the skin together with all affected tissue palmar and just dorsal to the neurovascular bundles and palmar to the tendon sheath on the flexor aspect of the finger. Some surgeons replace the skin of the proximal segment of the finger, others to above the middle phalanx. Another group uses smaller “firebreak” grafts, i.e., they only graft small areas, which causes fewer problems if the skin graft dies; however, it does mean that a smaller amount of pathologic tissue can be removed. Firebreak grafts do not appear to prevent recurrences any better than is achieved by LF without skin grafting (24). So far, no robust comparative studies have been carried out on outcomes of DF, including its different techniques. DF remains reserved for aggressive disease and recurrences. Wound healing takes longer than with LF and sensitivity is lost in the grafted area.

Cumulative complication rates were 17.4% [11.7; 23.1] for LF, 18.9 [--5.5; 43.3] for PNF, 78.0 [59.6; 96.4] for CCH injection, and 11.6 [0.0; 23.2] for DF (only a tenth of the number of patients were included for the latter) (e6). In relation to the minimally invasive procedures (PNF and CCH), some studies counted recurrences as a complication. The incidence of complications rises 10-fold for procedures to treat recurrences, with nerve injuries increasing in particular (27).

Postoperative splint treatment

Regarding rehabilitation after surgery, there is no high-quality evidence for the efficacy of night splints after LF or DF (24, e7, e8).

After PNF, in which the fibrosis is only divided but not removed, clinical experience suggests that night position splints or immobilizing gloves can stabilize the results, but no robust study data exist.

Radiotherapy

Radiotherapy is very effective in inhibiting proliferating fibroblasts and can “freeze” early stages of disease, and at least delay progression of more advanced stages.

In Tubiana stage N (fibrosis without flexion contracture) and N/1 (extension deficit 1° to 10°), there is very good evidence for the efficacy of radiotherapy, with approximately 80% disease control and 25% remission (e9e11). For more pronounced flexion contractures (up to 45°), significantly lower efficacy of radiotherapy has been described: higher rates of renewed progression are reported as follow-up time increases. Therapeutically, various fractionation regimens have become established, for example, 30 Gy in 2 series of 5 fractions versus 21 Gy in 1 series of 7 fractions (e12). Acute side effects reported were a transient skin reaction in 25% of patients and temporary dry desquamation in 2.5%. In 14%, skin dryness occurred as a late complication (e12).

Regarding adjuvant radiotherapy to prevent recurrence after surgery, no data exist from prospective or randomized studies. However, in patients at high risk of recurrence, radiotherapy can be carried out as an “individualized attempt at healing” once wound healing is complete, based on close consultation between patient, surgeon, and radiotherapist.

With ionizing radiation there is always the possibility that mutations and hence potentially fatal tumors can be triggered, and for this reason it is very important to assess this risk. Extensive conservative risk calculations show that, for a middle-aged person, radiotherapy will increase the risk of fatal cancer within the statistically expected life span by 0.02%–0.05% (e13, e14). For younger people (25 years) this risk must be doubled, for older people (over 60 years) it can be halved. For each individual patient, this risk needs to be explained and set against the burden of disease so that an informed decision can be made.

Treatment algorithm, counseling, and decision-making

As the evidence increases, designing a treatment algorithm has become easier. Every hand surgeon should be able to offer both, minimally invasive procedures such as PNF or CCH, if available, and more invasive procedures such as SF, LF, and DF, and to explain their advantages and disadvantages to the patient. It is essential to include the patient’s goals and wishes in the discussion and come to a joint decision.

Painful fibrosis without extension deficit can usually be treated by the wearing of padded, pressure-distributing fingerless gloves. Radiotherapy is also available to halt progression in these early stages.

In general, surgery should only be performed when contractures have developed that the patient experiences as impairing function. This can vary greatly from one person to another; for example, a patient’s occupation will have a strong influence on his or her ability or willingness to live with an extension deficit (e.g., pianist versus construction worker). Patients’ requirements for postoperative healing and use of their hand can vary just as much.

With contractures, minimally invasive treatment almost always leads to a good result with rapid recovery and return to everyday life without incurring high costs. Although the outcome of this treatment is not long-lasting, which is a disadvantage, the treatment can almost always be repeated with similar results.

Where primary contractures are severe (total extension deficit over 90° and isolated PIP contracture over 60°), minimally invasive treatments are less effective. For a patient who prefers a long-lasting result, or wants troublesome fibrosis removed in addition to contracture correction, and accepts a longer recovery time, LF (figure 2) is preferable.

Figure 2.

Figure 2

Intraoperative findings after limited fasciectomy. The palmar skin was not opened up completely, so that perforators of the vessels that travel with dermal nerve branches to the skin can be spared, contributing to better wound healing. Apart from this, a limited fasciectomy was carried out removing all affected fascial structures in the operative area.

In young patients with a family history in which both parents are affected and in whom severe contractures and concomitant diseases such as diabetes mellitus are present, primary dermofasciectomy can be considered because early recurrence after PNF and even LF occurs more frequently in this group. However, the patient has to accept loss of sensitivity in the grafted areas.

Where multiple fingers are affected to varying degrees, different surgical techniques can be combined to achieve the patient’s desired outcome without compromise in terms of complications (figure 3). This “modular technique,” – for example, combining SF and/or LF on some rays and PNF on others (figure 3) – is becoming a valuable option for patients who want minimally invasive treatment with rapid recovery, even though they have advanced or recurrent disease. It is also useful in high-risk patients with diabetes, severe nicotine abuse, or on anticoagulant medication, which increase the risk of postoperative complications.

Figure 3.

Figure 3

Example of the use of “modular technique” combining SF, LF with skin transposition, and PNF

a) Preoperative photograph: 67-year-old patient with advanced primary Dupuytren’s disease Tubiana or Iselin stage 4 (diabetic, heavy smoker, wheelchair-dependent)

b) Intraoperative result after a procedure combining percutaneous needle fasciotomy, fasciectomy, and limited fasciectomy with Z-plasty. Minimally invasive PNF was combined with SF and LF including local Z-plasty, achieving a good result for the patient without major surgery and without skin grafting. The patient wanted to be able to use his wheelchair independently again, which had become impossible because of the contractures, but preferred to avoid major surgery if possible as he was aware that he was at high risk of wound healing problems. The surgical areas where each technique was used are marked in the image on the right.

LF, limited fasciectomy; PNF, percutaneous needle fasciotomy; SF, segmental fasciectomy

Predicting the natural course of the disease and the time interval from surgery to recurrence in the individual case remains difficult and should be an object of future studies, as should comparisons between the different surgical techniques. To allow this, it will be essential to establish a uniform definition of the multiple measurement methods and definitions (e15) of clinical improvement and recurrence used in the literature to date.

Table 2. Overview of treatment options, escalating from conservative to surgical, showing results, recurrence rates, complications, and return-to-work.

Treatment (references)/ levels of evidence*3 Indication Result*1 Wound healing/ return to work*2 Complications(primary interventions)*5 Recurrence rate*1 Disadvantages*1
Conservative
Padded fingerless gloves Palmar fibrosis with no contracture Symptom relief
Radiotherapy (49–54)
Cohort studies
Oxford level of evidence 2b
Early stage, preventive (may be an option postoperatively in aggressive disease) Significant slowing of progression Erythema 25%
Dry skin 2.5%
Very rarely triggers malignant tumor
20% after 8.5 years for Tubiana stages N and N/1, for later stages 80% after 8.5 years Multiple sessions

(Low) risk of tumor induction
Collagenase
(41–43, 46)
RCTs
Oxford level of evidence 1b
Currently not licensed in Germany 60%–85% reduction of flexion contracture 1–10 days Cumulative rate 78%*4
Local edema 62%
Hematoma 25%
Skin wounds 24%
Lymph node enlargement 15%
Tendon damage 4%
65%
in 3 years
80%
in 7.5 years
Expensive

Efficacy varies between individuals Relatively high recurrence rate
Surgical
Percutaneous needle fasciotomy
(24, 25, 3239, 46)
RCTs
Oxford level of
?evidence 1b
Cords with flexion contracture
Patients wanting rapid return of function after treatment
65%–85% reduction of flexion contracture 1–5 days Cumulative rate 19%*4
Skin wounds 20%
Local edema 6%
Nerve damage 2%
Infection 1%
CRPS 1%
Vascular damage < 1%
Lymph node enlargement 0%
65% in
32 months
Relatively high recurrence rate
Selective/limited fasciectomy
(2327, 2931, 46)
Cohort studies
Oxford level of
?evidence 2b
> 20–30° flexion contracture 80% reduction of flexion contracture 2–4 weeks Cumulative rate 17%
Local edema 10%
CRPS 10%
Joint stiffness 10%
Flap necrosis 10%
Infection 7%
Wound dehiscence 5%
Vascular damage 4%
Nerve damage 3%
Hematoma 3%
Skin wounds 1%
12%–73%
in 5 years
Complications causing greater long-term impairment than PNF or collagenase

Longer wait until function is restored
Dermofasciectomy
(24, 25, 40, 41, 46)
Case series/cohort study
Oxford level of evidence 2b/4
Recurrence after SF/LF
Aggressive disease in young patients with risk factors
Comparable to SF/LF 3–8 weeks Cumulative rate 12%
Wound dehiscence 10%
Skin wounds 8%
CRPS 4%
Vascular damage 6%
Nerve damage 6%
Hematoma < 1%
Infection 0%

Local edema n.d.
Joint stiffness n.d.
8.4%
in 6 years
Loss of sensitivity in the grafted area

Scar at the skin graft donor site

Longer wait until function is restored

*1 Percentages and times given are based on different study populations and are therefore not fully comparable; in some cases, mean values from several studies are given.

*2 Mean empirical values without complications for light manual work are given; for heavy manual work with maximum load the time, where this is given, is longer for all treatments. There are no robust figures on this in the literature.

*3 Regarding the level of evidence, a Cochrane review (24) and one other systematic review (25) are available. For each treatment technique, the level of evidence given is based on the quality of the studies available for that technique.

*4 For the minimally invasive procedures (PNF and CCH), in some studies recurrences that occurred during the follow-up period were counted as complications, significantly increasing the cumulative incidence. Even complications not requiring treatment, such as skin tears for PNF and local swelling for collagenase, were carefully recorded.

*5 The incidence of complications increases 10-fold for interventions for recurrent disease, except after previous treatment with PNF or CCH (27).

CCH, collagenase Clostridium histolyticum (CCH treatment); CRPS, complex regional pain syndrome; LF, limited fasciectomy; n.d., no data; PNF, percutaneous needle fasciotomy; RCT, randomized controlled trial; SF, segmental fasciectomy

Questions on the article in issue 46/2022: Dupuytren’s Disease—Etiology and Treatment.

The submission deadline is 18 November 2022. Only one answer is possible per question.

Please select the answer that is most appropriate.

Question 1

What is the estimated worldwide prevalence of Dupuytren’s disease?

  1.  2%

  2.  4%

  3.  6%

  4.  8%

  5. 10%

Question 2

Genetic factors play a role in the etiology of Dupuytren’s disease. What is the extent of the contribution of genetic factors to the development of this disease?

  1. 10%

  2. 20%

  3. 40%

  4. 60%

  5. 80%

Question 3

Which of the following are possible findings in Tubiana stage 4 disease?

  1. Fibrosis without functional impairment

  2. Fibrosis and an extension deficit greater than 135°

  3. Palmar fibrosis without extension impairment

  4. No fibrosis and a mild extension deficit of 5°

  5. Fibrosis and an extension deficit of 25°

Question 4

Which disease is associated with Dupuytren’s disease?

  1. Hypertension

  2. Helicobacter pylori infection

  3. Diabetes mellitus

  4. Ankylosing spondylitis

  5. Hyperlipidemia

Question 5

Which activity, if performed long-term, is a risk factor for developing Dupuytren’s disease?

  1. Working with vibrating tools

  2. Spending time in cold-storage rooms

  3. Working in a damp environment

  4. Heavy lifting

  5. Skin contact with allergens

Question 6

Which surgical procedure is regarded as the reference standard in the treatment of Dupuytren’s disease?

  1. Limited fasciectomy

  2. Dermofasciectomy

  3. Percutaneous needle fasciectomy

  4. Radical fasciectomy

  5. Selective/segmental fasciectomy

Question 7

What is a common complication after surgical treatment of Dupuytren’s disease?

  1. Impaired circulation

  2. Stiffness

  3. Hyperesthesia

  4. Hyperalgesia

  5. Tremor

Question 8

What is the cumulative complication rate after limited fasciectomy?

  1. 5%

  2. 9%

  3. 13%

  4. 17%

  5. 21%

Question 9

Under certain conditions, radiotherapy may be given. For which stage of disease is there good evidence for this intervention?

  1. Stage 2 (Meyerding)

  2. Stage 3 (Meyerding)

  3. Stage 4 (Iselin)

  4. Stage 3 (Tubiana)

  5. Stage N (Tubiana)

Question 10

Which of the following is a disadvantage of percutaneous needle fasciotomy?

  1. Longer recovery time

  2. Loss of sensibility over a greater area

  3. Higher recurrence rate

  4. Extensive scarring

  5. Extensive hematoma

Acknowledgments

Translated from the original German by Kersti Wagstaff

Footnotes

Conflict of interest statement

Prof. Hermann has received consultancy fees from Novo College/Novo Cure.

Prof. Werker has received consultancy fees from Fidia Ltd, Italy.

The other authors declare that they have no conflict of interest.

References

  • 1.Hueston JT. Recurrent Dupuytren’s contracture. Plast Reconstr Surg. 1963;31:66–69. doi: 10.1097/00006534-196301000-00008. [DOI] [PubMed] [Google Scholar]
  • 2.Rombouts JJ, Noel H, Legrain Y, Munting E. Prediction of recurrence in the treatment of Dupuytren’s disease: evaluation of a histologic classification. J Hand Surg Am. 1989;14:644–652. doi: 10.1016/0363-5023(89)90183-4. [DOI] [PubMed] [Google Scholar]
  • 3.Balaguer T, David S, Ihrai T, Cardot N, Daideri G, Lebreton E. Histological staging and Dupuytren’s disease recurrence or extension after surgical treatment: a retrospective study of 124 patients. J Hand Surg Eur. 2009;34:493–496. doi: 10.1177/1753193409103729. [DOI] [PubMed] [Google Scholar]
  • 4.Salari N, Heydari M, Hassanabadi M, et al. The worldwide prevalence of the Dupuytren disease: a comprehensive systematic review and meta-analysis. J Orthop Surg Res. 2020;15 doi: 10.1186/s13018-020-01999-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Nordenskjöld J, Englund M, Zhou C, Atroshi I. Prevalence and incidence of doctor-diagnosed Dupuytren’s disease: a population-based study. J Hand Surg Eur Vol. 2017;42:673–677. doi: 10.1177/1753193416687914. [DOI] [PubMed] [Google Scholar]
  • 6.Ng M, Thakkar D, Southam L, et al. A genome-wide association study of Dupuytren disease reveals 17 additional variants implicated in fibrosis. Am J Hum Genet. 2017;101:417–427. doi: 10.1016/j.ajhg.2017.08.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Flatt AE. The Vikings and Baron Dupuytren’s disease. Baylor University Medical Center. Proc. 2001;14:378–384. doi: 10.1080/08998280.2001.11927791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.McFarlane RM. On the origin and spread of Dupuytren’s disease. J Hand Surg Am. 2002;27:385–390. doi: 10.1053/jhsu.2002.32334. [DOI] [PubMed] [Google Scholar]
  • 9.Dolmans GH, Werker PM, Hennies HC, et al. Wnt signaling and Dupuytren’s disease. N Engl J Med. 2011;365:307–317. doi: 10.1056/NEJMoa1101029. [DOI] [PubMed] [Google Scholar]
  • 10.Larsen S, Krogsgaard DG, Aagaard Larsen L, Iachina M, Skytthe A, Frederiksen H. Genetic and environmental influences in Dupuytren’s disease: a study of 30 330 Danish twin pairs. J Hand Surg Eur. 2015;40:171–176. doi: 10.1177/1753193414535720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Mohede DCJ, Riesmeijer SA, de Jong IJ, Werker PMN, van Driel MF. Prevalence of Peyronie and Ledderhose diseases in a series of 730 patients with Dupuytren disease. Plast Reconstr Surg. 20201;45:978–984. doi: 10.1097/PRS.0000000000006642. [DOI] [PubMed] [Google Scholar]
  • 12.Broekstra DC, Groen H, Molenkamp S, Werker PMN, van den Heuvel ER. A systematic review and meta-analysis on the strength and consistency of the associations between Dupuytren disease and diabetes mellitus, liver disease and epilepsy. Plast Reconstr Surg. 2018;141:367e–379e. doi: 10.1097/PRS.0000000000004120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Broekstra DC, van den Heuvel ER, Lanting R, Harder T, Smits I, Werker PMN. Dupuytren disease is highly prevalent in male field hockey players aged over 60 years. Br J Sports Med. 2018;52:1327–1331. doi: 10.1136/bjsports-2016-096236. [DOI] [PubMed] [Google Scholar]
  • 14.Descatha A, Carton M, Mediouni Z, et al. Association among work exposure, alcohol intake, smoking and Dupuytren’s disease in a large cohort study (GAZEL) BMJ Open. 2014;4 doi: 10.1136/bmjopen-2013-004214. e004214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Descatha A, Jauffret P, Chastang JF, Roquelaure Y, Leclerc A. Should we consider Dupuytren’s contracture as work-related? A review and meta-analysis of an old debate. BMC Musculoskelet Disord. 2011;12 doi: 10.1186/1471-2474-12-96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Mathieu S, Naughton G, Descatha A, Soubrier M, Dutheil F. Dupuytren’s disease and exposure to vibration: systematic review and meta-analysis. Joint Bone Spine. 2020;87:203–207. doi: 10.1016/j.jbspin.2020.02.001. [DOI] [PubMed] [Google Scholar]
  • 17.Fadel M, Leclerc A, Evanoff B, et al. Association between occupational exposure and Dupuytren’s contracture using a job-exposure matrix and self-reported exposure in the CONSTANCES cohort. Occup Environ Med. 2019;76:845–848. doi: 10.1136/oemed-2019-105912. [DOI] [PubMed] [Google Scholar]
  • 18.Malsagova AT, Zwanenburg RL, Werker PMN. New insights into the anatomy at the palmodigital junction in Dupuytren’s disease: the palmodigital spiralling sheet. J Hand Surg Eur. 2019;44:972–978. doi: 10.1177/1753193419863418. [DOI] [PubMed] [Google Scholar]
  • 19.Zwanenburg RL, Werker PMN, McGrouther DA. The anatomy and function of Cleland’s ligaments. J Hand Surg Eur. 2014;39:482–490. doi: 10.1177/1753193413511944. [DOI] [PubMed] [Google Scholar]
  • 20.Zwanenburg RL, McGrouther DA, Werker PMN. Grayson ligament: a revised description of its anatomy and function. J Hand Surg Am. 2019;44:341e1–341e6. doi: 10.1016/j.jhsa.2018.07.002. [DOI] [PubMed] [Google Scholar]
  • 21.Hettiaratchy S, Tonkin MA, Edmunds IA. Spiralling of the neurovascular bundle in Dupuytren’s disease. J Hand Surg Eur. 2010;35:103–108. doi: 10.1177/1753193409349855. [DOI] [PubMed] [Google Scholar]
  • 22.Dickie WR and Hughes NC. Dupuytren’s contracture: a review of the late results of radical fasciectomy. Br J Plast Surg. 1967;20:311–314. doi: 10.1016/s0007-1226(67)80055-9. [DOI] [PubMed] [Google Scholar]
  • 23.Davis TR. Surgical treatment of primary Dupuytren’s contractures of the fingers in the UK: surgeons’ preferences and research priorities. J Hand Surg Eur. 2013;38:83–85. doi: 10.1177/1753193412467170. [DOI] [PubMed] [Google Scholar]
  • 24.Rodrigues JN, Becker GW, Ball C, Zhang W, Giele H, Hobby J, Pratt AL, Davis T. Surgery for Dupuytren’s contracture of the fingers. Cochrane Database Syst Rev. 2015 Dec 9; doi: 10.1002/14651858.CD010143.pub2. CD010143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Soreide E, Murad MH, Denbeigh JM, et al. Treatment of Dupuytren’s contracture: a systematic review. Bone Joint J. 2018;100:1138–1145. doi: 10.1302/0301-620X.100B9.BJJ-2017-1194.R2. [DOI] [PubMed] [Google Scholar]
  • 26.Poelstra R, van Kooij YE, van der Oest MJW, et al. Patient’s satisfaction beyond hand function in Dupuytren’s disease: analysis of 1 106 patients. J Hand Surg Eur. 2020;45:280–285. doi: 10.1177/1753193419890284. [DOI] [PubMed] [Google Scholar]
  • 27.Denkler K. Surgical complications associated with fasciectomy for Dupuytren’s disease: a 20-year review of the English literature. Eplasty. 2010;10 [PMC free article] [PubMed] [Google Scholar]
  • 28.Werker PM, Pess GM, van Rijssen AL, Denkler K. Correction of contracture and recurrence rates of Dupuytren contracture following invasive treatment: the importance of clear definitions. J Hand Surg Am. 2012;37:2095–2105. doi: 10.1016/j.jhsa.2012.06.032. [DOI] [PubMed] [Google Scholar]
  • 29.Moermans JP. Segmental aponeurectomy in Dupuytren’s disease. J Hand Surg Br. 1991;16:243–254. doi: 10.1016/0266-7681(91)90047-r. [DOI] [PubMed] [Google Scholar]
  • 30.Clibbon JJ, Logan AM. Palmar segmental aponeurectomy for Dupuytren’s disease with metacarpophalangeal flexion contracture. J Hand Surg Br. 2001;26:360–361. doi: 10.1054/jhsb.2001.0602. [DOI] [PubMed] [Google Scholar]
  • 31.Moermans JP. Long-term results after segmental aponeurectomy for Dupuytren’s disease. J Hand Surg Br. 1996;21:797–800. doi: 10.1016/s0266-7681(96)80195-1. [DOI] [PubMed] [Google Scholar]
  • 32.Van Rijssen AL, Gerbrandy FS, Ter Linden H, Klip H, Werker PM. A comparison of the direct outcomes of percutaneous needle fasciotomy and limited fasciectomy for Dupuytren’s disease: a 6-week follow-up study. J Hand Surg Am. 2006;31:717–725. doi: 10.1016/j.jhsa.2006.02.021. [DOI] [PubMed] [Google Scholar]
  • 33.Therkelsen LH, Skov ST, Laursen M, Lange J. Percutaneous needle fasciotomy in Dupuytren contracture: a register-based, observational cohort study on complications in 3 331 treated fingers in 2 257 patients. Acta Orthop. 2020;91:326–330. doi: 10.1080/17453674.2020.1726057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Van Rijssen AL, Ter Linden H, Werker PMN. Five-year results of a randomized clinical trial on treatment in Dupuytren’s disease: percutaneous needle fasciotomy versus limited fasciectomy. Plast Reconstr Surg. 2012;129:469–477. doi: 10.1097/PRS.0b013e31823aea95. [DOI] [PubMed] [Google Scholar]
  • 35.Zhou C, Selles RW, Slijper HP, et al. Comparative effectiveness of percutaneous needle aponeurotomy and limited fasciectomy for Dupuytren’s contracture: a multicenter observational study. Plast Reconstr Surg. 2016;138:837–846. doi: 10.1097/PRS.0000000000002560. [DOI] [PubMed] [Google Scholar]
  • 36.Van Rijssen AL, Werker PM. Percutaneous needle fasciotomy for recurrent Dupuytren disease. J Hand Surg Am. 2012;37:1820–1823. doi: 10.1016/j.jhsa.2012.05.022. [DOI] [PubMed] [Google Scholar]
  • 37.Mendelaar NHA, Poelstra R, van Nieuwenhoven CA, et al. Outcome of recurrent surgery in Dupuytren’s disease: comparison with initial treatment. Plast Reconstr Surg. 2019;144:828e–835e. doi: 10.1097/PRS.0000000000006150. [DOI] [PubMed] [Google Scholar]
  • 38.Warwick D. Dupuytren’s disease: my personal view. J Hand Surg Eur. 2017;42:665–672. doi: 10.1177/1753193417715773. [DOI] [PubMed] [Google Scholar]
  • 39.Eaton C. Percutaneous fasciotomy for Dupuytren’s contracture. J Hand Surg Am. 2011;36:910–915. doi: 10.1016/j.jhsa.2011.02.016. [DOI] [PubMed] [Google Scholar]
  • 40.Herrera FA, Benhaim P, Suliman A, Roostaeian J, Azari K, Mitchell S. Cost comparison of open fasciectomy versus percutaneous needle aponeurotomy for treatment of Dupuytren contracture. Ann Plast Surg. 2013;70:454–456. doi: 10.1097/SAP.0b013e31827e531d. [DOI] [PubMed] [Google Scholar]
  • E1.Skov ST, Bisgaard T, Søndergaard P, Lange J. Injectable collagenase versus percutaneous needle fasciotomy for Dupuytren contracture in proximal interphalangeal joints: a randomized controlled trial. J Hand Surg Am. 2017;42:321–328. doi: 10.1016/j.jhsa.2017.03.003. [DOI] [PubMed] [Google Scholar]
  • E2.Strömberg J, Ibsen Sörensen A, Fridén J. Percutaneous needle fasciotomy versus collagenase treatment for Dupuytren contracture: a randomized controlled trial with a two-year follow-up. J Bone Joint Surg Am. 2018;100:1079–1086. doi: 10.2106/JBJS.17.01128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • E3.Scherman P, Jenmalm P, Dahlin LB. Three-year recurrence of Dupuytren’s contracture after needle fasciotomy and collagenase injection: a two-centre randomized controlled trial. J Hand Surg Eur. 2018;43:836–840. doi: 10.1177/1753193418786947. [DOI] [PubMed] [Google Scholar]
  • E4.Hueston JT. Digital Wolfe grafts in recurrent Dupuytren’s contracture. Plast Reconstr Surg Transplant Bull. 1962;29:342–344. doi: 10.1097/00006534-196204000-00005. [DOI] [PubMed] [Google Scholar]
  • E5.Armstrong JR, Hurren JS, Logan AM. Dermofasciectomy in the management of Dupuytren’s disease. J Bone Joint Surg Br. 2000;82:90–94. doi: 10.1302/0301-620x.82b1.9808. [DOI] [PubMed] [Google Scholar]
  • E6.Krefter C, Marks M, Hensler S, Herren DB, Calcagni M. Complications after treating Dupuytren’s disease. A systematic literature review. Hand Surg Rehabil. 2017;36:322–329. doi: 10.1016/j.hansur.2017.07.002. [DOI] [PubMed] [Google Scholar]
  • E7.Larson D, Jerosch-Herold C. Clinical effectiveness of postoperative splinting after surgical release of Dupuytren’s contracture: a systematic review. BMC Musculoskelet Disord. 2008;9 doi: 10.1186/1471-2474-9-104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • E8.Jerosch-Herold C, Shepstone L, Chojnowski AJ, Larson D, Barrett E, Vaughan SP. Night-time splinting after fasciectomy or dermo-fasciectomy for Dupuytren’s contracture: a pragmatic, multi-centre, randomized controlled trial. BMC Musculoskelet Disord. 2011;12:136–140. doi: 10.1186/1471-2474-12-136. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • E9.Keilholz L, Seegenschmiedt MH, Born AD. Sauer R, editor. Radiotherapie im frühen Stadium des Morbus Dupuytren. Indikation und Langzeitergebnisse. Strahlenther Onkol. 1997;173:27–35. doi: 10.1007/BF03039191. [DOI] [PubMed] [Google Scholar]
  • E10.Fachgruppenspezifische evidenzbasierte S2e-Leitlinie der Deutschen Gesellschaft für Radioonkologie (DEGRO) Version 2.0 vom 02.11.2018. www.degro.org/wp-content/uploads/2018/11/S2-Leitlinie-Strahlentherapie-gutartiger-Erkrankungen-update-2018-Endversion.pdf (last accessed on 22 October 2021) [Google Scholar]
  • E11.Betz N, Ott OJ, Adamietz B, Sauer R, Fietkau R, Keilholz L. Radiotherapy in early-stage Dupuytren’s contracture. Long-term results after 13 years. Strahlenther Onkol. 2010;186:82–90. doi: 10.1007/s00066-010-2063-z. [DOI] [PubMed] [Google Scholar]
  • E12.Seegenschmiedt MH, Keilholz L, Wielpütz M, Schubert CH, Fehlauer F. Eaton C, editor. Long-term outcome of radiotherapy for early stage Dupuytren’s disease: a phase III clinical study (chapter 44) Dupuytren’s disease and related hyperproliferative disorders. Heidelberg. Springer-Verlag. 2012::349–371. [Google Scholar]
  • E13.Estimate of the risk of cancer caused by radiation therapy of Dupuytren’s disease. www.dupuytren-online.de/downloads/Krebsrisiko_durch_Strahlentherapie_des_Morbus_Dupuytren.pdf (last accessed on 19 October 2021) [Google Scholar]
  • E14.Jansen JT, Broerse JJ, Zoetelief J, Klein C, Seegenschmiedt HM. Estimation of the carcinogenic risk of radiotherapy of benign diseases from shoulder to heel. Radiother Oncol. 2005;76:270–277. doi: 10.1016/j.radonc.2005.06.034. [DOI] [PubMed] [Google Scholar]
  • E15.Karpinski M, Moltaji S, Baxter C, Murphy J, Petropoulos J-A, Thoma A. A systematic review identifying outcomes and outcome measures in Dupuytren’s disease research. J Hand Surg Eur. 2020;45 doi: 10.1177/1753193420903624. [DOI] [PubMed] [Google Scholar]
  • E16.Malsagova AT, Zwanenburg RL, Werker PMN. New insights into the anatomy at the palmodigital junction in Dupuytren’s disease: the palmodigital spiralling sheet. J Hand Surg Eur. 2019;44:972–978. doi: 10.1177/1753193419863418. [DOI] [PubMed] [Google Scholar]
  • E17.Short WH, Watson HK. Prediction of the spiral nerve in Dupuytren’s contracture. J Hand Surg Am. 1982;7:84–86. doi: 10.1016/s0363-5023(82)80020-8. [DOI] [PubMed] [Google Scholar]
  • E18.Zwanenburg RL, Werker PMN, McGrouther DA. The anatomy and function of Cleland’s ligaments. J Hand Surg Eur. 2014;39:482–490. doi: 10.1177/1753193413511944. [DOI] [PubMed] [Google Scholar]
  • E19.Zwanenburg RL, McGrouther DA, Werker PMN. Grayson ligament: a revised description of its anatomy and function. J Hand Surg Am. 2019;44:341e1–341e6. doi: 10.1016/j.jhsa.2018.07.002. [DOI] [PubMed] [Google Scholar]
  • E20.Hettiaratchy S, Tonkin MA, Edmunds IA. Spiralling of the neurovascular bundle in Dupuytren’s disease. J Hand Surg Eur. 2010;35:103–108. doi: 10.1177/1753193409349855. [DOI] [PubMed] [Google Scholar]

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