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Book cover for Handbook of Surgical Consent Handbook of Surgical Consent
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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always … More Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages and recommendations are for the non-pregnant adult who is not breastfeeding.

Axillary lymph node dissection 180

Management of breast abscess 182

Reduction mammoplasty 184

Implant-based breast reconstruction 187

Deep inferior epigastric perforator flap (DIEP flap) 189

Excision biopsy of breast lump/lumpectomy 191

Surgery for nipple discharge (microdochectomy/major duct excision) 193

Latissimus dorsi myocutaneous flap reconstruction 196

Mastectomy 199

Sentinel lymph node biopsy 202

Transverse rectus abdominis myocutaneous flap (TRAM flap) 204

Wide local excision of breast tumour 207

Axillary nodal status is the single most important prognostic indicator of systemic relapse in breast cancer. This is routinely assessed with a preoperative ultrasound scan and FNA analysis of any pathological nodes. Axillary lymph node dissection (ALND) remains the gold standard of managing clinically positive axillary lymph nodes or following a positive sentinel lymph node biopsy.1

Anatomically, the axilla can be divided into three zones (Fig. 6.1):

Level I nodes: inferior to pectoralis minor

Level II nodes: posterior to pectoralis minor

Level III nodes: superior to pectoralis minor

 Breast and axillary anatomy.
Fig. 6.1

Breast and axillary anatomy.

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.115, Figure 2.6.

Routine practice involves the dissection of lymph nodes up to level II, where level III clearance may be selectively carried out in the presence of extensive level II lymph node metastases.

Access to the axilla is best achieved via a 5–8cm horizontal or vertical incision. When performing a mastectomy, the axillary contents are reached via the same mastectomy wound as a continuation of the axillary tail of the breast.

Dissection involves incising the clavipectoral fascia to gain access to the axillary contents. Lateral border of pectoralis major is identified and the plane between the lateral chest wall and the axilla is created. On the posterior aspect of this space, the long thoracic nerve (nerve to serratus anterior) is identified and preserved. The dissection is continued cranially to the apex of the axilla where the axillary vein forms the superior boundary of level I nodes. Care must be taken to avoid avulsion of branches of the lateral thoracic vein from the main axillary vein trunk as troublesome bleeding will be encountered.

At this point, the thoracodorsal pedicle is identified and preserved. All axillary tissue is swept caudally off the axillary vein and laterally to the medial border of the latissimus dorsi (LD) muscle, which forms the lateral border of the axilla. Access to level III nodes can be aided by abduction and flexion of the shoulder, which relaxes the fibres of pectoralis major and minor. Where possible, axillary contents are dissected off en bloc. The intercostobrachial nerve traverses the middle of the axilla. Attempt should be made to preserve this nerve unless heavy involvement with nodal metastases may require it to be sacrificed.

Good haemostasis is ensured and routine use of a closed suction drain is common practice. Wound closure is carried out in layers using absorbable sutures.

Wound infection

Bleeding and haematoma formation

Lymphoedema (rates of up to 20%)

Venous thrombosis (axillary vein)

Sensory loss medial aspect of upper arm (intercostobrachial nerve palsy; >50%)

Arm stiffness (20–30%)

Chronic pain

Winging of the scapula (long thoracic nerve palsy—rare)

Arm weakness (thoracodorsal nerve or long thoracic nerve injury—rare)

None (but group and save recommended)

General anaesthesia

Infiltration of local anaesthesia into the wound for postoperative analgesia

Routine postoperative wound check

Review of histology and decision for adjuvant treatments

Aspiration of seroma or haematoma if symptomatic

1. National Institute for Health and Clinical Excellence. NICE Guidance: Early and Locally Advanced Breast Cancer. London: NICE, 2009.
2. Mansel RE, Fallowfield L, Kissin M, et al. Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial. J Natl Cancer Inst 2006;98(9):599–609.reference

Breast abscesses can be broadly divided into lactational and non-lactational causes. An abscess can complicate up to 10% of lactational mastitis and may affect up to 2.5% of breastfeeding mothers. The commonest cause of non-lactational breast abscess is periductal mastitis. Smoking is the strongest risk factor for this. An abscess may also arise from infective exacerbation of skin lesions (e.g. sebaceous cysts or hidradenitis suppurativa). Presentation of mastitis or a breast abscess in postmenopausal women should raise the suspicion of an inflammatory carcinoma and when tolerated, routine triple assessment should be completed.

The principal pathway of managing breast abscesses is by non-operative means. Serial ultrasound guided aspiration (± washout) of the abscess cavity is augmented with an appropriate antibiotic cover.1 This commonly achieves a successful resolution of the abscess with superior cosmetic outcomes compared with incision and drainage. Occasionally, an ultrasound-guided insertion of a percutaneous drain may be required for large abscess cavities.

Overall, a formal incision and drainage is seldom required. For this, the core principles of ‘adequate drainage’ apply. Commonly access to the abscess cavity can be achieved through a small incision, although any overlying necrotic skin may require an excision. The cavity is washed out with copious amounts of saline and gently packed with an appropriate dressing. Use of a drain is rarely required. Wounds can be partly closed to aid healing by secondary intention. Attempt at delayed primary closure should be carefully considered as it carries a high risk of abscess recurrence. A specimen of pus or tissue from the cavity should be sent for microbiological analysis in order to direct appropriate antibiotic cover.

Indications for an incision and drainage of a breast abscess include:

Complex abscess cavity not amenable to ultrasound drainage

Recurrent/multiloculated abscess cavity

Large abscess with significant overlying skin necrosis

Bleeding from the cavity

Recurrence of abscess requiring further drainage

Formation of chronic, multiloculated collection. Long-term this may lead to a mammary duct fistula or a chronically discharging sinus

Scarring with a poor cosmetic outcome

None

Image-guided aspiration/drainage carried out under local anaesthesia

Surgical drainage carried out under general anaesthesia

Daily wound irrigation, packing of cavity to allows healing by secondary intention

A delayed primary closure can be considered if wound remains clean and dry to aid faster healing of skin

Where a non-infective aetiology is suspected (e.g. inflammatory carcinoma or underlying ductal carcinoma in situ (DCIS) with comedo necrosis), definitive triple assessment is mandatory

1. Dixon JM. Outpatient treatment of non-lactational breast abscess. Br J Surg 1992;79(1):5.reference

Reduction mammoplasty is a common cosmetic procedure used to reduce the size and alter the shape of the breast.

The indications for a reduction mammoplasty include:

Symptomatic gigantomastia (e.g. resulting in chronic shoulder, neck and back pain, persistent intertrigo, shoulder grooving/ulceration from bra straps)

Virginal breast hypertrophy (have high rate of recurrence following surgery)

Gynaecomastia

Patient preference/to improve cosmesis

As part of contralateral symmetrization after breast reconstruction

Recently, mammoplasty techniques have been amalgamated with oncological breast surgery as part of oncoplastic breast surgery. This has broadened the application of breast-conserving surgery, allowing for wide excisions of the tumour, while maintaining the optimal breast shape.

To date several different mammoplasty techniques have been described. Common to all is the reduction in breast volume that is achieved by excision of skin, fat, and glandular tissue, with subsequent repositioning of the nipple–areolar complex (NAC).

Some of the commonly utilized techniques include:

The Wise pattern mammoplasty (Fig. 6.2)—this remains the most popular technique allowing for safe excision of large volumes of glandular tissue. Maintaining an adequate dermoglandular pedicle (commonly inferior or superomedial pedicle) preserves the blood supply to the NAC. The resultant scar has an inverted ‘T’ shape

(Lejour)1  vertical mammoplasty—this technique is a modification of the technique described by Lassus2 and further popularized by Hall-Findlay,3 excises the bulk of breast tissue directly inferior to the NAC. The breast envelope is reapproximated, leaving a vertical scar only

The ‘Round-block’ (Benelli)4  technique—this technique involves a periareolar incision and excision of a ‘donut’ of breast tissue. Reapproximation of the periareolar incision allows for a more discrete scar. The procedure can be combined with an augmentation mammoplasty to correct any ptosis. Limitations remain in the amount of glandular tissue that may be excised

 Reduction mammoplasty (Wise pattern).
Fig. 6.2

Reduction mammoplasty (Wise pattern).

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.133, Figure 2.13.

The choice of the techniques is dependent on patient as well as surgeon factors. The breast tissue is commonly excised using sharp dissection (with a knife) or with the use of diathermy. Excessive bleeding can be minimized by infiltration of breast tissue with a diluted adrenaline solution (typically 1:1000 solution). Care is required to preserve an adequate width of the dermoglandular pedicle in order to preserve nipple–areolar viability. Careful haemostasis is of paramount importance. The routine use of suction drains have not been show to alter outcomes.

Early bleeding/haematoma formation requiring re-exploration (∼5%)

Wound infection

Wound dehiscence (specially the T-junction scar in a Wise pattern mastectomy)

Change in sensation of nipple (30–40%)

Nipple loss (1–5%)

Scarring (including widened/hypertrophic or keloid scars)

Poor cosmesis

Inability to breastfeed

None (group and save sufficient)

General anaesthesia

Local anaesthetic infiltration for postoperative analgesia

Routine postoperative review to ensure satisfactory wound healing and cosmetic outcome

Following oncoplastic surgery, review of final histological results and plans for adjuvant therapies required

1. Lejour M. Verical mammoplasty and liposuction of the breast. Plast Reconstr Surg. 1994;94(1):100–14.reference
2. Lassus C. A technique for breast reduction. Int Surg 1970;53(1):69–72.reference
3. Hall-Findlay EJ. A simplified vertical reduction mammoplasty: shortening the learning curve. Plast Reconstr Surg 1999;104(3):748–59.reference
4. Benelli L. A new periareolar mammoplasty: the ‘round block’ technique. Aesthetic Plast Surg 1990;14(2):93–100.reference

Implant-based breast reconstructions are a frequently performed technique and according to recent national data, account for 37% of all immediate and 16% of delayed reconstructions following a mastectomy.1

The key advantages of implant reconstructions are the relatively short operative time and quicker postoperative recovery. However, unlike autologous reconstructions, the cosmetic outcome can be variable and the volume and projection of the reconstructed breast can be limited. Furthermore, the effects of radiotherapy to the final aesthetic result are significant where implants have been used. The pros and cons of implant-based reconstruction need to be clearly outlined to the patient prior to surgery.

The principal consideration of an implant-based reconstruction is whether there is adequate implant cover beneath the mastectomy skin flaps. The placement of the implant in the subpectoral space (posterior to the pectoralis major) is deemed the gold standard. However, this space is limited and therefore tissue expanders are often used to create a larger submuscular space.

The access to the subpectoral space is carried out by a muscle-splitting approach along the fibres of pectoralis major or via its lateral free border with the chest wall (Fig. 6.3). Careful submuscular dissection is performed with special attention to haemostasis. Once the implant is positioned in place, muscle fibres are closed over it for complete coverage. Post-operatively, the tissue expander is gradually filled with saline over several weeks, until the desired volume is reached. A number of adjustable implants/expanders (e.g. Becker adjustable implant) allow for a single stage procedure, where the injection port can be removed once the desired volume is reached.

 Implant-reconstruction post skin-sparing mastectomy.
Fig. 6.3

Implant-reconstruction post skin-sparing mastectomy.

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.140, Figure 2.18.

The standard approach is a two-staged procedure where at the second stage, adjustments the implant capsule (capsulotomy) can be made and the tissue expander is a replaced for a definitive fixed volume implant. The critical area of inadequate muscle cover is the inferior border of pectoralis major, where additional implant cover is achieved using a dermal sling as part of a Wise pattern mastectomy or an acellular dermal allograft (e.g. Alloderm). This also allows the use of fixed-volume implants in the immediate reconstruction setting and allows the implant to sit lower on the chest wall thus achieving a better natural shape.

Implants may also be used to augment an autologous reconstruction (specially an LD flap) in cases where the volume of autologous tissue available may not be adequate to achieve symmetry with the contralateral breast.

Contralateral symmetrization surgery

Capsulotomy and replacement of tissue expander implant for a definitive implant (two-stage reconstruction)

Wound infection

Periprosthetic infection

Bleeding and haematoma formation

Seroma

Capsular contracture (may be de novo or as consequence of periprosthetic infection or concurrent postoperative chest wall radiotherapy)

Postoperative pain

Implant/tissue expander failure (rare)

Poor cosmetic outcome

Need for revision surgery to improve cosmetic outcome (estimated 40% risk of requiring further surgery over a 4-year period)

None

General anaesthesia

Wound check to ensure healing of mastectomy scar

Review of histology and plans for adjuvant therapies

Serial instillation of saline into the expander implant to achieve the desired volume and projection

1. Clinical Effectiveness Unit, The Royal College of Surgeons of England, Association of Breast Surgery at the British Association of Surgical Oncology, British Association of Plastic, Reconstructive and Aesthetic Surgeons, Royal College of Nursing, and The NHS Information Centre for health and social care. Second National Mastectomy and Reconstruction Audit, NHS National Information Centre, 2009.

Attempts at reducing the donor site morbidity from transverse rectus abdominis myocutaneous (TRAM) flaps led to the development of muscle-sparing techniques and later the deep inferior epigastric perforator (DIEP) free flap. It was first described by Allen and Treece in 1992.1 Today, DIEP represents the gold standard method for autologous free flap breast reconstruction, using abdominal tissue.

Potentially any woman who has had a mastectomy is candidate for DIEP flap reconstruction. Relative contraindications include a history of heavy smoking, previous long transverse or oblique abdominal incisions or where one or both deep inferior epigastric vessels have been ligated. The need for post-mastectomy radiotherapy has been shown in several series to result in an inferior cosmetic results in all reconstruction, although autologous reconstructions are deemed more resistant. There is as yet no concrete evidence to suggest radiotherapy may lead to delayed flap necrosis and thus it is not considered a contraindication.

The DIEP flap is based on the deep inferior epigastric vessels, from which two rows of arteries and veins perforate the rectus abdominis muscle on each side to supply the ipsilateral skin and subcutaneous fat. Preoperative cross-sectional imaging has been shown to help accelerate flap harvesting and to potentially identify a dominant superficial inferior epigastric systems. Preoperative markings delineate the boundaries of the breast/mastectomy cavity and the length of abdominal flap. The latter is similar to the marking of an abdominoplasty.

The abdominal flap is harvested with identification of the lateral and medial rows of the deep inferior epigastric perforators. These are then traced down to their origin, between the fibres of the rectus abdominis muscle and with full preservation of muscle function and innervation. With the vascular pedicle to the free flap isolated, it is transported to the chest and a microvascular anastomosis is fashioned to the internal mammary (and occasionally the thoracodorsal) vessels. For a bilateral reconstruction, tissue from the two halves of the abdomen needs to be harvested on separate perforator pedicles.

The flap is appropriately inset in the mastectomy cavity and the skin envelope resected to fit the mastectomy flaps. The incised anterior rectus sheath is reapproximated using a non-absorbable suture. The umbilicus is sutured in its new position and the abdominal wound closed over two suction drains.

Higher-level postoperative care is essential for regular monitoring of flap viability in the first 24–48h. Low index of suspicion should be kept for a possible haematoma and/or problems with the vascular anastomosis. Early return to theatre for an exploration is an important determinant of salvaging a threatened free flap.

Limited restriction of activity with graded physiotherapy (i.e. raising arms, lifting etc.) for at least 6 weeks postoperatively is associated with a reduction in recipient complication rates.

If an adequate calibre perforator vessel is absent—conversion of the procedure to a free TRAM flap

Complications of a DIEP flap reconstruction are divided into general, donor site, and flap-related problems

General complications

Deep vein thrombosis ± pulmonary embolism (long procedure and prolonged immobility)

Basal atelectasis/postoperative pneumonia (poor respirator function and splinting of diaphragm due to donor site pain and tightness of abdominal closure)

Donor site complications

Seroma

Haematoma

Wound dehiscence and wound infection

Umbilical necrosis (1–5%)

Pain and discomfort due to tightness of abdominal wound

Abdominal hernia (0.6–1.4%)

Flap related complications

Haematoma

Thrombosis

Early re-exploration for flap related problems (6%)

Partial (2.5%) or complete flap failure (1%)

Fat necrosis and loss of flap volume (13%)

None (but group and save is needed)

General anaesthesia (often local anaesthetic has to be infiltrated at donor site on completion of the procedure)

Meticulous wound care and maintenance of physiology to optimize flap perfusion and reduce donor/recipient site complications in the perioperative and the immediate postoperative period

Routine postoperative wound check

Following an immediate reconstruction, review of final histology and plans for an any adjuvant treatment is needed

Nipple-areolar reconstruction

1. Allen RJ, Treece P. Deep inferior epigastric perforator flap for breast reconstruction. Ann Plast Surg 1994;32:32.reference

The outcome of the triple assessment for a breast lesion dictates the surgical therapy that ensues. In some circumstances, the preoperative assessment may yield inconclusive or indeterminate results thus requiring an excision biopsy to confirm the histological diagnosis. Where a lesion is preoperatively proven to be benign, decision to excise the lesion may be due to patient preference, the size of the lesion (e.g. a large (>2cm) fibroadenoma) or suspicious clinical features. Both approaches involve an excision of the target lesion with minimal disruption of surrounding normal breast tissue.

Current guidelines of the Association of Breast Surgery recommend that a preoperative diagnosis is achieved in over 90% of cases and that excision biopsy is confined to no greater than 25g of tissue.1 Small impalpable lesions may need to be preoperatively localized using ultrasound marking and/or wire-guided techniques.

Excision of a proven benign lesion due to:

Patient preference

Large lesions resulting in a cosmetic defect

Suspicious clinical history

Lesions with indeterminate or atypical histology (B3) on preoperative assessment (e.g. ADH, ALH, ductal hyperplasia of usual type) or suspicious clinical features

Presence of a radial scar (associated with presence of atypia or malignancy)2,3

Infection

Bleeding

Poor cosmetic outcome

Need for further surgery

None

General anaesthesia (generally allows for faster lesion localization and better patient compliance)

Local anaesthesia feasible for small but easily palpable lesions (infiltration of local anaesthesia may result in the lesion becoming difficult to find)

Routine wound check (this can be performed safely by the community team/GP) in benign cases

Multidisciplinary review of histology, specially where preoperative assessment was suspicious or indeterminate

Further excision may be required if malignancy is confirmed and microscopic resection margins are deemed inadequate

1. Association of Breast Surgery. Surgical guidelines for management of breast cancer. Eur J Surg Oncol 2009;35(Suppl 1):1–22.reference
2. Radial scar—also known as a complex sclerosing lesion.
3. Kennedy M, Masterson AV, Kerin M, et al. Pathology and clinical relevance of radial scars: a review. J Clin Pathol 2003;56(10):721–4.reference

Nipple discharge accounts for approximately 5% of breast clinic referrals, of which 5% may be caused by underlying in situ or malignant disease. Nipple discharge may be coloured, from a single or multiple ducts. Serosangiunous/bloody discharge from a single duct may be associated with a papilloma, ductal hyperplasia, or carcinoma. More commonly the discharge is found to be physiological and associated with underlying duct ectasia.

The assessment of nipple discharge aims to differentiate between benign physiological discharge and ductal pathology. The principal mode of investigation remains the ‘triple assessment’. This is augmented by a number of non-surgical techniques that include ductoscopy, ductography, and ductal lavage, but these are seldom used in routine practice. The surgical management of nipple discharge can be diagnostic as well as therapeutic. The two main approaches include microdochectomy (the approach for a single duct discharge) or major duct excision.

Persistent blood-stained single duct discharge (in woman of child-bearing age planning to breastfeed)

Presence of ductal lesion identified on ductography or ductoscopy

Persistent multiple duct discharge (may be bloody or non-blood stained)

Persistent single duct discharge in a woman of non-childbearing age

Treatment of recurrent periductal mastitis

Management of physiological nipple inversion

Due to the abundance of ductal flora, antibiotic prophylaxis is often used. There is no evidence to support the routine use of antibiotic therapy postoperatively.

The approach to the mammary ducts can be achieved either via a radial incision or more commonly using a circumareolar incision (typically three-fifths to half of the areolar circumference). In a microdochectomy, it is important to express the duct discharge in theatre in order to identify the offending duct. The duct is then isolated using a lacrimal probe or via injection of methylene blue into the duct.

Ductoscopy can also be used to illuminate the relevant duct. A 2–3cm length of the duct is isolated and excised. Care should be taken to prevent excision/damage to the neighbouring normal ducts.

In a total duct excision (Hadfield's procedure), all ducts are excised from the underside of the nipple. The specimen includes the surrounding breast tissue to a depth of approximately 2cm behind the NAC (Fig. 6.4). A purse-string dermal suture behind the nipple can be used to minimize nipple inversion. Incisions are closed in layers using absorbable suture.

 Key breast anatomy.
Fig. 6.4

Key breast anatomy.

Reproduced with permission from Gardiner MD and Borley NR. Training in Surgery. 2009. Oxford: Oxford University Press, p.43, Figure 3.2.

Failure to identify the single duct in microdochectomy—conversion to a major duct excision

If malignancy is histologically confirmed—an appropriate oncological resection

Change/reduction in sensation of nipple (up to 40%)

Nipple inversion and poor cosmesis

Nipple ischaemia (<1%)

Recurrent discharge

Difficulty/problems breastfeeding

None

General anaesthesia

Routine postoperative wound check

Review of histology and plans for further treatment

Assessment of cure from symptoms (i.e. persistent discharge)

1. Dixon JM (ed.) A Companion to Specialist Surgical Practice—Breast Surgery, Edinburgh: Elsevier, 2006, p265.

The LD myocutaneous flap (Fig. 6.5) was first described by Tansini in 1896. Over the years it has become a popular and versatile option for covering a large mastectomy defect, either as an autologous reconstruction or with the use of implant to augment its volume. The flap is based on the thoracodorsal vessels that enter the muscle just below its insertion into the humoral head.

 Latissimus dorsi (LD) flap.
Fig. 6.5

Latissimus dorsi (LD) flap.

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.137, Figure 2.15.

Preoperative markings include that of the boundaries of the breast/mastectomy cavity and the skin paddle of the LD flap on the back. The orientation of the skin paddle is largely dependent on the patients shape and may be horizontal (along the bra straps) or oblique (using natural skin folds).

The LD flap is harvested with the patient position in the lateral position. The marked skin paddle is incised and the skin and superficial fascia is dissected off the proximal and distal boundaries of the muscle. The anterior edge of the LD muscle is identified and dissected off the chest wall. The muscle is detached from its distal attachment above the iliac crest and posteriorly from the paravertebral muscles.

The thoracolumbar fascia is left intact as incising it may increase donor site morbidity and the risk of a lumbar herniation. Dissection of the hilum of the muscle involves careful preservation of vascular braches of the pedicle to serratus anterior and more importantly the main thoracodorsal pedicle. Anterior mobility of the flap is achieved by dividing the synsarcosis between the LD muscle and teres major and/or division of the tendinous insertion of LD. Routine division of the thoracodorsal nerve at this point is recommended by some to prevent problems with flap animation. A subcutaneous tunnel is created as high up as possible in the axilla to transmit the flap into the mastectomy cavity.

The donor site is closed in layers over suction drains. The flap is appropriately inset, the skin paddle trimmed and sutured to the mastectomy flaps. In an implant-augmented reconstruction, the LD muscle provides total muscle coverage of the implant. An extended LD reconstruction is a variation that aims to provide a larger volume of tissue for a complete autologous reconstruction.1 This approach harvests a greater degree of subfascial fat but also recruits serratus, scapular, and iliac fat pads to gain additional autologous volume.

Postoperative care involves careful observation for flap viability in the first 24–48h, good level of hydration and oxygenation and gradual mobilization of the patient.

Nipple–areolar reconstruction

Contralateral symmetrization procedure

Complication can be divided into donor site and flap-related problems:

Flap-related

Haematoma

Partial or complete flap failure (<1%)

Thrombosis

Fat necrosis

Muscle atrophy and asymmetry due to loss of flap volume

Flap animation (as result of tethering of the LD muscle and intact function of thoracodorsal nerve)

Donor site

Skin flap necrosis

Wound dehiscence

Seroma formation

Haematoma formation

Arm weakness (related to absence of a functional LD muscle)

Chronic donor site pain

None

Group and save

General anaesthesia (with infiltration of local anaesthetic for postoperative analgesia)

Routine postoperative check to ensure satisfactory wound healing and removal of suction drains from the donor site if still in situ

Drainage of donor site seroma (or haematoma)

If an expander implant is used in a two-stage procedure, tissue expansion is commenced once wounds have healed

In the immediate reconstruction setting, the final histology and the plans for adjuvant treatment are reviewed and discussed with the patient

Nipple–areolar reconstruction can be planned for a later date

1. Delay E, Gounot N, Bouillot A, et al. Autologous latissimus breast reconstruction: a 3-year clinical experience with 100 patients. Plast Reconstr Surg 1998;102(5):1461–78.reference

Mastectomy is the removal of all breast tissue and some overlying skin including the NAC (Fig. 6.6). Historically, Halstedian theory dictated that breast cancer is a locoregional disease and therefore surgery would include a radical excision of all breast tissue and locoregional axillary nodes, as well as the underlying chest wall musculature (pectoralis major and minor).

 Simple mastectomy with lateral fish tail extension (to remove redundant lateral skin flap.
Fig. 6.6

Simple mastectomy with lateral fish tail extension (to remove redundant lateral skin flap.

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.127, Figure 2.11.

More recently Fisherian theory of breast cancer has changed the paradigm of treatment from a locoregional disease to that of systemic control. For this locoregional control would again take the shape of excising breast tissue and relevant regional lymph nodes, while maintaining the integrity of the underlying structures posterior to the mammary gland.

Indications for mastectomy:

Large tumour where breast-conserving surgery not feasible or likely to result poor cosmetic outcome

Inflammatory carcinoma

Multicentricity (tumour deposits in more than one quadrant of the breast)

Risk-reducing surgery (e.g. BRCA gene mutation carriers)

Patient preference

Modern-day practice encompasses the following mastectomy techniques:

Simple mastectomy: involves excision of the breast, the overlying skin and NAC only

Modified radical mastectomy (Patey's mastectomy): involves excision of the breast, overlying skin including NAC, and axillary node dissection (division of pectoralis minor is seldom required)

Skin-sparing mastectomy: this approach removes all breast tissue (± relevant axillary glands), while maintaining maximum amount of chest wall skin required for a subsequent reconstruction

Subcutaneous (nipple-sparing) mastectomy: this technique removes all subcutaneous breast tissue while preserving the NAC. Controversy remains regarding the oncological safety of preserving the nipple. Intra-operative frozen section analysis of retroareolar tissue may be used to ensure clear resection margins although the false-negative rate of this technique has been questioned. Therefore this approach is often used selectively, especially in risk-reducing surgery or where the risk of recurrence is estimated to be low. Careful counselling of the patient regarding the risks of local recurrence is the key

Wise pattern mastectomy: this technique amalgamates the standard Wise pattern reduction mammoplasty skin excision and a skin-sparing mastectomy to ultimately reduce the skin envelope of a large breast

Following appropriate preoperative planning and skin marking (this would include consideration for reconstruction, degree of skin involvement by tumour etc.), dissection is carried out through the skin and dermis. The ‘mastectomy’ plane of dissection and the thickness of the mastectomy skin flaps are dependent on the adiposity of the patient

Careful marking of the breast boundaries is vital in order to prevent over-dissection of the mastectomy cavity, especially if immediate reconstruction is planned. Adherence to the correct plane of dissection ensures adequate oncological resection yet preserving the subdermal vascular plexus that is vital to for skin flap viability. Posterior dissection in the retromammary space should ensure preservation of the fascia over pectoralis major muscle. Dissection of the axillary tail would give access to the contents of the axilla where concurrent axillary surgery can be performed through the same wound

In skin-sparing mastectomy, the dissection of breast tissue is carried out through a circumareolar incision. In a subcutaneous (nipple-sparing approach), a subareolar incision would allow dissection of the NAC free from the remaining breast tissue. The remainder of the dissection is carried out as previously outlined

Meticulous haemostasis is mandatory. Use of closed suction drains in the mastectomy cavity is a universally practice. Closure of the wound is carried out in layers using absorbable sutures

If there is involvement of the chest wall—(partial) excision of the underlying pectoralis muscle

Breast reconstruction which may be immediate or delayed—current NICE and British Association of Surgical Oncology guidelines recommend all women being offered reconstructive options if considered for a mastectomy

Seroma

Haematoma

Mastectomy flap necrosis

Wound infection (usually consequent to the flap necrosis)

Poor cosmetic outcome

Group and save is sufficient

General anaesthesia

Postoperative analgesia—there are several options

Local anaesthetic skin infiltration, bathing the mastectomy cavity with local anaesthetic fluid infused via the cavity drains

Regional nerve blocks (e.g. paravertebral blocks)

Routine postoperative check to ensure satisfactory wound healing ± removal of suction drains

Review of histology and plans of adjuvant treatment

Plastic surgical review if immediate reconstruction undertaken

Planning for nipple–areolar reconstruction

Counselling and planning for a delayed reconstruction

The sentinel lymph node is defined as the first node that directly drains the primary tumour. Evidence to date has shown that up to 85% of all stage breast cancers to be node negative, thus patients undergoing an unnecessary axillary clearance. Furthermore, routine ALND carries significant morbidity with no impact on survival. Sentinel lymph node biopsy (SLNB) is an alternative, minimally invasive approach to ALDN that has become the standard of care in prognosticating early, clinically node- negative breast cancer.

The results of the ALMANC trial have so far shown overall lower morbidity and a shorter hospital stay in patient undergoing SLNB compared with ALND.1

Currently, the only absolute contraindications to SLNB are clinically node-positive disease and the presence of previous mastectomy (without axillary surgery). The standard of care for patients with a positive sentinel lymph node (tumour focus of >0.2mm) is to undergo an axillary clearance or axillary radiotherapy. The oncological implications of isolated tumour cells (tumour focus <0.2mm) is currently unknown and therefore such patients are treated as SLNB negative and require no further surgery.

Recently, there has been growing interest in techniques for intraoperative analysis of sentinel lymph nodes. Such approach has been shown to avoid repeat surgery, improve patient satisfaction and reduce delays to adjuvant treatment. The techniques used include frozen section analysis and more recently, molecular techniques such as reverse transcriptase polymerase chain reaction (RT-PCR).

Current NICE guidelines recommend that SLNB is carried out by a team that is validated in the use of the technique as identified by the NEW START programme.2,3 This programme has standardized the protocol for sentinel node mapping. It involves dual localization of the sentinel lymph node(s) using technetium-99 labelled nanocolloid and Paten V blue dye.

Access to the axilla can be incorporated into the WLE scar or via a small (commonly <5cm) de novo incision in the axilla. Minimal disruption of the axillary contents is the key. Using a handheld G-probe, any hot (measured G-radiation count >x10 background) and/or blue node is excised for histological (or intraoperative) analysis. Meticulous haemostasis is mandatory. The routine use of a suction drain is not indicated. Closure of the wound in layers follows standard practice.

Axillary node clearance in sentinel lymph node-positive patients

Adjuvant chemotherapy or radiotherapy

Wound infection

Haematoma and seroma formation

Axillary vein thrombosis (in deeper dissections)

Lymphoedema (overall rate = 5%)2

Sensory loss (intercostobrachial nerve palsy—11% at 12 months)2

Shoulder stiffness (<10%)2

Allergy to Paten V blue dye (0.9%)4

Permanent skin staining with blue dye (<1%)

Failure to localize the sentinel node (false negative rate <5%)

None necessary

General anaesthesia (with infiltration of local anaesthetic into wound for postoperative analgesia)

Routine postoperative wound check

Assessment of histology and plans for adjuvant treatment

Aspiration of seroma or haematoma (if symptomatic)

1. National Institute for Health and Clinical Excellence. NICE Guidance: Early and Locally Advanced Breast Cancer. London: NICE, 2009.
2. Mansel RE, Fallowfield L, Kissin M, et al. Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial. J Natl Cancer Inst 2006;98(9):599–609.reference
3. Raven Department of Education. NEW START Sentinel Lymph Node Biopsy Training Programme. Royal College of Surgeons, England (Programme now closed).
4. Barthelmes L, Goyal A, Newcombe RG, et al. and NEW START and ALMANAC study groups. Adverse reactions to patent blue V dye—The NEW START and ALMANAC experience. Eur J Surg Oncol 2010;36(4):399–403.reference

The TRAM flap is an axial pattern pedicle flap popularized following its first description by Hartrampf in 1982.1 It utilizes a paddle of skin and underlying rectus abdominis muscle, which is mobilized on its pedicle, the deep superior epigastric vessels.

However, it carries two main disadvantages. First, harvesting of significant amounts of rectus sheath and rectus abdominis muscle results in loss of abdominal wall integrity and potential for development of a hernia. The second is the relative unpredictability of the blood supply of any skin harvested beyond the muscle boundary.

Nonetheless, it provides ample tissue for autologous reconstruction of a breast, negating the need for augmentation with an implant. Modifications of this technique include muscle-sparing and the free TRAM flaps, the former resulting in lower risk donor site morbidity related to the abdominal wall. The current practice of using DIEP free flaps has become the gold standard of autologous breast reconstruction using abdominal tissue, and TRAM flaps are seldom used.

The TRAM flap (Fig. 6.7) can be used in both the immediate and delayed reconstruction setting. The preoperative skin marking on the abdomen involves a symmetrical abdominal skin ellipse similar to that of an abdominoplasty, within which the skin paddle of the flap is delineated. The myocutaneous flap on the one side of the abdomen provides autologous tissue for the contralateral breast reconstruction.

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.138, Figure 2.16

Careful dissection of skin and dermis preserves the midline-perforating vessels above and below the umbilicus, as well as the subdermal plexus that ensures maximal viability of the skin paddle. Inferiorly, the belly of rectus abdominis is isolated and transected, with ligation of the inferior epigastric vessels. Superiorly the anterior rectus sheath is divided and the muscle and the overlaying fat and skin are elevated. A subcutaneous tunnel from the abdominal wound to the mastectomy cavity transmits the flap, which is then appropriately inset and sutured to the mastectomy skin flaps.

The donor site defect is closed by approximating the anterior rectus sheet superiorly with non-absorbable suture (e.g. no 1. nylon). The defect in the inferior part of the rectus sheath is repaired with a tension free mesh closure. Transposition of the umbilicus on its stalk to its new position concludes closure of the superficial abdominal wound layers. Use of a closed suction drain in the abdominal wound is routine practice.

These can be divided into flap related or donor site related complications:

Donor site

Haematoma

Seroma

Abdominal wound infection and/or dehiscence

Abdominal wall weakness or frank hernia formation

Dehiscence/necrosis of umbilicus

Flap related

Partial or total flap failure

Poor cosmetic outcome

Fat necrosis and loss of flap volume (often related to flap blood supply)

Upper abdominal bulging and discomfort related to subcutaneous tunnelling of the flap

Group and save

General anaesthesia (with infiltration of local anaesthetic to donor site wound for postoperative analgesia)

Routine postoperative check to ensure adequate wound healing

Interval check to ensure satisfactory cosmetic outcome/degree of symmetry with contralateral breast and planning for nipple reconstruction

1. Hartrampf CR, Scheflan M, Black PW. Breast reconstruction with a transverse abdominal island flap. Plast Reconstr Surg 1982;69(2):216–25.reference

Wide local excision is a term that is synonymous with breast-conserving surgery (BCS), whereby an oncological resection is performed while maintaining as normal a breast shape (Fig. 6.8). There are no national guidelines regarding the thickness of resection of margins and locally agreed protocols are followed. Generally, the aim is to achieve macroscopic resection margins of at least 1cm and microscopic resection margins of 1mm and 2mm for invasive and in situ carcinoma, respectively. Evidence to date supports the fact that overall local recurrence and survival rates in BCS with postoperative radiotherapy are comparable with that of mastectomy alone.

 Breast local excision—(a) wide local excision, (b) segmental excision.
Fig. 6.8

Breast local excision—(a) wide local excision, (b) segmental excision.

Reproduced with permission from Chaudry MA and Winslet MC. Oxford Specialist Handbook of Surgical Oncology. 2009. Oxford: Oxford University Press, p.121, Figure 2.9.

The principal determinant of a satisfactory cosmetic outcome following a WLE is the proportion of breast tissue that is excised in relation to the total breast size. A resection of greater than 20% of the breast volume significantly impacts the aesthetic outcomes. Therefore recently, a number of plastic surgical techniques have been amalgamated with the oncological breast surgery, with the aim to widen the spectrum of applicability of BCS. These approaches are collectively termed ‘oncoplastic breast surgery’ and use a myriad of volume displacement, volume replacement and mammoplasty techniques to achieve the optimal aesthetic outcome while avoiding a mastectomy.

Contraindications to a WLE (or BCS) include multicentricity (presence of cancer in more than one quadrant), a high tumour to breast volume ratio (relative contraindication), and inflammatory carcinoma.

Small, impalpable lesions may require preoperative localization (e.g. ultrasound marking or wire-guided localization). An appropriately placed incision is a key principle in oncoplastic surgery. This minimizes poor cosmetic outcomes and allows for maximum access to the lesion. The full thickness resection aims to achieve macroscopically clear radial margins, and anterior (skin) and posterior (chest wall) margins may be considered less important as postoperative radiotherapy is planned.

Although a number of surgeons would leave the cavity unfilled, this almost always results in poor cosmetic outcomes especially after radiotherapy. Use of oncoplastic techniques with volume displacement techniques helps to obliterate this potential cavity.1 Where a long subcutaneous tunnel to the lesion is created or where oncoplastic techniques are use to fill the excision cavity, use of titanium clips (e.g. Ligaclips™) help in directing radiotherapy planning.

Careful haemostasis is mandatory. Use of closed suction drains is sometimes required, especially to drain large areas of subcutaneous undermining. The wound is closed in layers using absorbable suture.

Concurrent axillary surgery (sentinel node biopsy or axillary clearance as indicated)

Contralateral symmetrization surgery (performed as an immediate or delayed procedure)

Reoperative surgery if adequate macroscopic margins not achieved

Seroma or haematoma formation

Wound infection (or development of an infected seroma or haematoma)

Fat necrosis (specially in volume displacement oncoplastic techniques)

Poor scaring/cosmetic outcome (this may be exaggerated after radiotherapy)

Change in sensation of nipple (where periareolar/circumareolar incision used)

Loss of nipple viability (complication of mammoplasty techniques in oncoplastic surgery)

Not required/group and save

General anaesthesia

Local anaesthesia (± sedation) may be feasible in selective cases

Routine postoperative check to ensure adequate wound healing/management of haematoma or seroma formation

Review of histology and planning for adjuvant treatment

Long-term review of cosmetic outcomes and requirements for contralateral symmetrization surgery

1. Clough KB, Kaufman GJ, Nos C, et al. Improving breast cancer surgery: a classification and quadrant per quadrant atlas of oncoplastic surgery. Ann Surg Oncol 2010;17(5):1375–91.reference
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