Reconstruction Using Local Flaps for Penoscrotal Defects after Ablation of Skin Lesions

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J Wound Manag Res. 2018;14(1):37-43

Publication date (electronic) : 2018 March 30

doi : https://doi.org/10.22467/jwmr.2017.00220

Hyunwoo Kyung, Hyeokjae Kwon, Seung-Han Song, Sang-Ha Oh

Department of Plastic and Reconstructive Surgery, Chungnam National University School of Medicine, Daejeon, Korea

Corresponding author: Hyunwoo Kyung, M.D. Department of Plastic and Reconstructive Surgery, Chungnam National University Hospital, 282 Munhwa-ro, Jung-gu, Daejeon 35015, Korea Tel: +82-42-280-7380 Fax: +82-42-280-7384 E-mail: hwkyung@gmail.com

Received 2017 November 1; Revised 2017 December 26; Accepted 2018 January 24.

Abstract

Introduction

Penoscrotal defects are associated with a variety of conditions, including extramammary Paget disease (EMPD), Fournier’s gangrene (FG), and skin cancer. Careful reconstruction of the penoscrotal region is vital for sexual and urological functions [1]. The aims of reconstruction are to assist wound healing and provide adequate function and acceptable appearance. However, reconstruction of penoscrotal defects is difficult because of the variety of skin colors and thicknesses, the presence of bacterial flora, difficulty in immobilization, and complicated contours [1]. Therefore, a variety of approaches must be used for reconstruction, which are based on the size, position, and severity of the defect and the availability of surrounding tissue.

We reconstructed penoscrotal defects using local advancement scrotal flaps, skin grafting, anterolateral thigh (ALT) flaps, and internal pudendal artery perforator (IPAP) flaps and obtained satisfactory results. The purpose of the study was to review and analyze the results of our patients who underwent reconstruction of penile and scrotal defects.

Methods

Patients

We performed a retrospective chart review of 13 patients who underwent penoscrotal reconstruction from January 2012 to May 2016. The defects were caused by EMPD in 10 patients, FG in 2 patients, and skin cancer in 1 patient. All patients underwent radical debridement. We applied a negative-pressure-wound-therapy (NPWT) device to facilitate wound healing and evacuation of discharges in selected patients who had a large wound defect and massive discharge. The defect areas ranged from 4 to 225 cm² (mean 75.0 cm²). The reconstructive procedures were performed using split-thickness skin grafts (STSGs) and scrotal advancement, ALT, and IPAP flaps. The patients’ demographic and clinical data are listed in Table 1.

Table 1.

Demographic and clinical data of the patients

Results

The ages of patients ranged from 46 to 93 years (mean 67.5±14.5 years). The duration of follow-up ranged from 12 to 36 months (mean 18.5 months). Eight cases had a defect of the penile shaft that was repaired by an STSG. Seven cases who had no tension when the scrotal defect was approximated underwent repair using a scrotal advancement flap. A distant flap was performed for large scrotal defects that involved the surrounding tissue; 3 cases underwent repair by a pedicled ALT flap, and 3 patients underwent repair by an IPAP flap. The lengths of the flaps ranged from 2 to 20 cm (mean 9.5 cm), and the widths ranged from 2 to 15 cm (mean 6.9 cm). All of the flaps survived without reports of severe complications such as total flap necrosis or congestion that required immediate surgery. Minor complications (hematoma or wound dehiscence) occurred in 3 patients, which healed after a minor surgical procedure.

Case presentations

Case 2

A 74-year-old man presented with a 2-year history of a pruritic erythematous skin lesion on his penis and a scrotal skin lesion. A skin biopsy confirmed the diagnosis of EMPD. After complete excision of the lesions, the resulting penile 56-cm²(8×7 cm), scrotal 35-cm² (5×7 cm), and pubic-region 180-cm² (18×10 cm) defects were reconstructed by an STSG, scrotal flap, and pedicled ALT flap, respectively (Figs. 1, 2). At the 31-month follow-up visit, local recurrence of EMPD was not seen, and the aesthetic result was acceptable (Fig. 3).

Fig.1.

(Case # 2) A 74-year-old man with confirmed extramammary Paget disease. After complete excision, the areas of the penile, scrotal and pubic region defects were 56 cm² (8×7 cm), 35 cm² (5×7 cm), and 180 cm² (18×10 cm), respectively.

Fig.2.

(Case # 2) A split-thickness skin graft and scrotal flap were used to repair the penile shaft and scrotal defect. An anterolateral thigh flap was elevated from the left thigh and was transposed to the defect in the pubic region.

Fig.3.

(Case # 2) Six months after surgery. The penile, scrotal, and pubic defects were completely covered and healed.

Case 13

A 65-year-old man sustained FG, with soft tissue defects over the penile shaft and scrotum. After surgical debridement, the areas of the defects were approximately 42 cm² (7×6 cm) and 160 cm² (20×8 cm), respectively. An IPAP flap was constructed and transposed to the scrotal defect. The penile shaft defect was repaired by an STSG (Figs. 4, 5). At postoperative month 12, the flap had survived, and the aesthetic outcome was good (Fig. 6).

Fig.4.

(Case # 13) A 65-year-old man sustained Fournier’s gangrene with soft tissue defects over the penile shaft and scrotum. After surgical debridement, areas of the defects were approximately 42 cm² (7×6 cm) and 160 cm² (20×8 cm), respectively.

Fig.5.

(Case # 13) An internal pudendal artery perforator flap was constructed and transposed to the defect. The defect on the penile shaft was covered by a split-thickness skin graft.

Fig.6.

(Case # 13) Six months after reconstructive surgery, the scrotal and penile defect were completely covered and healed.

Discussion

The penoscrotal area has a special function that represents the confluence of urological, sexual, and gastrointestinal functions [1]. The scrotum allows testicular mobility, which reduces trauma and allows optimal thermal regulation for spermatogenesis [2]. The scrotum is constructed of specialized skin that is lined by the dartos muscle, which can contract to retain heat and relax to dissipate heat [2].

Penoscrotal defects may result from trauma, infection, or tumor ablation. FG is one of the most devastating types of infections. FG is a necrotizing fasciitis of the perineum and external genitalia that rapidly spreads along contiguous fascia. It often affects patients with serious comorbidities, including diabetes, alcoholism, and advanced age. In addition to cardiopulmonary support and broad-spectrum antibiotics, the standard treatment involves aggressive debridement of necrotic tissue. Consequently, reconstructive procedures are required for the resulting extensive skin and soft tissue defects [1].

EMPD is a rare cutaneous malignancy, and in men most frequently involves the penoscrotal area [3]. Defects due to tumor ablation are usually reconstructed immediately after the tumor is resected and the margin is confirmed free of malignancy. Wide excision and examination of frozen sections are needed to create and confirm tumor-free margins before reconstruction [3]. This type of surgery frequently leads to skin and soft tissue defects that are larger than expected.

Reconstruction of the penoscrotal region represents a surgical challenge because of the highly complex three-dimensional structures and the difficulties involved in achieving an esthetic appearance and normal functions. However, several reconstructive procedures can achieve wound coverage, including those using STSGs, local scrotal advancement flaps, and fasciocutaneous flaps [4].

Carvalho et al. [5] reported on a small defect of the scrotum that healed by secondary intention without surgical treatment. Parkash et al. [6] reported good results after a skin graft, but Carvalho et al. [5] reported that infection occurred in 18% and Chen et al. [4] reported that partial skin loss occurred in 11% of skin grafts. The reason for the higher rates of infection or skin loss after skin grafting in the penoscrotal region compared with other sites is probably accounted for by the difficulties in immobilization, the presence of bacterial flora, and the complicated structures [1]. For our patients, STSGs were only used to cover penile shaft defects.

Parkash et al. [6] reported a successful reconstruction that was achieved by a local scrotal advancement flap and reported that wound dehiscence and partial flap loss occurred as complications but resolved, with flap survival. The authors also used a scrotal flap for reconstruction if the scrotal defect could be approximated without tension. However, another type of reconstructive surgery is needed if the defect is large and the remaining scrotal skin cannot be advanced and the surrounding defect is accompanied.

A fasciocutaneous flap provides durable skin and allows coverage of a large area of exposed soft tissue. Therefore, it is more effective than an STSG for the reconstruction of scrotal and perineal defects. It also produces better functional outcomes and cosmetic results than skin grafting, with fewer contractures due to scarring [1]. We used pedicle ALT flaps in 6 patients and IPAP flaps in 3 patients. Both flaps have advantages in that they are relatively easy to construct, have a reliable blood supply, and are less bulky than other muscle flaps. In most cases, the donor site allowed primary closure. However, when the width of the ALT flap was large, a skin graft was performed for closure of the donor site. In addition, the construction of an ALT flap elevates a larger skin paddle than the IPAP flap, and a unilateral ALT flap can cover both exposed testicles. An ALT flap can be moved farther to cover the pubic area, so bilateral ALT flaps can be used for penoscrotal defects accompanied by defects in the pubic area. The IPAP flap should be used in a bilateral pattern when both testicles are exposed. For such cases, donor site scars are well concealed by both gluteal folds.

Table 2 summarizes our review of recent publications that have reported on reconstructive methods for defects of the penoscrotal area, and compares our study with the other case series. In 2007, Lee et al. [7] reported on reconstructions of penoscrotal defects by scrotal flaps, groin flaps, and pedicled ALT flaps. Yang et al. [8] reconstructed penoscrotal defects using superficial epigastric artery-based flaps and scrotal flaps. In 2010, Chen et al. [4] used gracilis muscle flaps and STSGs. In 2011, Chen et al. [9] reconstructed penoscrotal defects using conventional methods and pudendal thigh flaps. In 2014, Ahn et al. [1] performed reconstruction using LD free flaps and perforator-based flaps (IPAP flap) to repair penoscrotal defects. In addition, several published papers have reported on reconstruction of penoscrotal defects by the methods described so far. Currently, it appears that there is no general consensus on the methods used for reconstruction of penoscrotal defects. Thus, we recommend that the selection of an appropriate surgical procedure should be based on the location and size of the defect. Our flowchart for deciding on the appropriate procedure is shown in Fig. 7.

Table 2.

Studies reporting on reconstructive methods for penoscrotal defects

Fig.7.

Flowchart for reconstructing penoscrotal defects. STSG, split-thickness skin graft; ALT, anterolateral thigh; IPAP, internal pudendal artery perforator.

Conclusions

The appropriate reconstruction of a penoscrotal defect is vital for function and cosmesis. We used STSGs to repair defects on the penile shaft and local scrotal advancement flaps to repair relatively small scrotal defects. A distant flap was used for large defects that involved the surrounding tissue. Among distant flaps, the pedicled ALT flap can be used to reconstruct defects that expose both testicles, or the ALT flap can be mobilized to repair defects in the pubic area. An IPAP flap allows the donor site to be disguised within a gluteal fold. The authors suggest therefore, that a suitable approach for reconstruction of a penoscrotal defect is based on the size and position of the defect, and should involve a skin graft, scrotal flap, ALT flap, or IPAP flap.

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