Background
The scalp delineates the superior margin of the body, a position that is commonly exposed to considerable insults from the surrounding environment. Its exposed location, which is generally devoid of clothing coverage, makes the scalp susceptible to burns and other trauma that can produce extensive scarring and disfigurement. Additionally, the scalp is subject to a staggering variety of benign and malignant neoplasms, often as the result of years of sun exposure. Today, many scalp defects encountered prior to reconstruction are the product of ablative surgery, often Mohs micrographic surgery.
Tissues that are traumatized, irradiated, or infected surround many of these defects. Patients are frequently elderly with multiple medical problems that may limit their ability to tolerate certain procedures. Thus, the repair of a scalp defect can involve treatments ranging from the simplicity of a few sutures to a multi-month, multi-procedure reconstruction.
The decision-making process behind a successful outcome requires a solid knowledge of anatomy, a clear evaluation of the defect, the recognition of relevant patient attributes, and the knowledge of a variety of reconstruction options. Preoperative planning is imperative. Preoperative plans must be specifically tailored to the individual problem because no single solution is available for reconstructing the scalp.
An image depicting scalp anatomy can be seen below.
Scalp anatomy, demonstrating the several layers. Relevant Anatomy
The surgeon should clearly understand the elements of scalp anatomy before attempting reconstructive procedures. The scalp is defined as the anatomic area overlying the skull between the superior orbital rims anteriorly and the superior nuchal line posteriorly. This anatomic space is divided into hair-bearing and non–hair-bearing (ie, forehead) segments. The forehead further is divided into 5 subunits: the central, the left and right temporal, and the left and right brow subunits.
The soft tissue within this region is commonly divided into 5 layers: skin, subcutaneous tissue, aponeurosis (galea), loose areolar tissue, and pericranium. These layers easily are remembered using the mnemonic "SCALP" (see the image below). An external layer of thick skin is fixed to the underlying subcutaneous layer of fat. This subcutaneous layer is richly vascularized and provides a fibrous bridge to keep the skin tightly fixed to the galea aponeurosis (ie, epicranium) beneath. The galea aponeurosis is essentially the membranous tendon extension connecting the frontalis and occipitalis muscles, and it is the superficial musculoaponeurotic system (SMAS) layer of the scalp.
Scalp anatomy, demonstrating the several layers. The galea aponeurosis becomes an important layer clinically, especially with coronal defects through the galea, because the antagonistic forces of the frontalis and occipitalis muscles widely separate the wound edges. However, if the aponeurosis remains intact, skin retraction is much more limited. When reconstructing scalp defects, limiting separation of the galea from the overlying skin is important to avoid devascularizing the skin. Laterally, the galea becomes contiguous with the temporoparietal fascia (ie, superficial temporal fascia). The temporoparietal fascia is a richly vascularized layer that envelopes several key structures, notably the frontal branches of the facial nerve, the auriculotemporal nerve, and the superficial temporal artery and vein.
Below the galea is a layer of loose connective or areolar tissue. This layer provides for relatively free movement between the aponeurosis and the deepest layer, the pericranium. It also creates a point of separation during traumatic scalping injuries. The pericranium is composed of dense connective tissue tightly affixed to calvarial bone by Sharpey fibers. In general, these fibers are easy to strip off the underlying bone, although they may be strongly adherent along the cranial sutures. As the pericranium approaches the superficial temporal line laterally, it divides to form 2 layers, the temporalis muscle fascia (deep temporal fascia) and the pericranium of the temporal bone. These 2 layers together invest the body of the temporalis muscle. Inferior to the temporalis muscle, the temporalis fascia splits to invest the superficial temporal fat pad, and then it inserts into the zygomatic arch.
Although a rich network of anastomotic connections is present, the blood supply to the scalp is primarily derived from 5 pairs of arteries (see the image below). Arising from the ophthalmic artery and thus from the internal carotid artery, the supratrochlear and supraorbital arteries supply the forehead and anterior scalp. The external carotid gives rise to 3 pairs of arteries, the superficial temporal, postauricular, and occipital. These vessels are found in the subcutaneous layer immediately superficial to the galea with only minimal contributions to the deep pericranial layer. The pericranium is nourished via the middle meningeal and intracranial circulation to the calvarial bone. As a result, disruption of blood supply to the scalp does not result in calvarial bone necrosis. Venous drainage parallels the arterial system and eventually drains into the internal and external jugular veins.
The 5 pairs of arteries that supply the scalp. Interestingly, sensory innervation of the anterior scalp is derived from all 3 branches of the trigeminal nerve via the supraorbital and supratrochlear nerves (V1), the zygomaticotemporal nerve (V2), and the auriculotemporal nerve (V3). The posterior scalp receives sensory innervation from cervical sensory branches through the greater (C2) and lesser (C2, C3) occipital nerves.
Motor innervation to the forehead derives from the facial nerve. The frontal branch of the facial nerve exits the parotid gland running in an oblique line lateral to the lateral orbital rim to supply the frontalis, corrugator supercilii, and procerus muscles. A posterior auricular branch of the facial nerve provides function to the occipitalis muscle. Motor branches, which are the deep temporal branches of the mandibular nerve (V3), innervate the temporalis muscle.
Lymphatic drainage of the scalp runs primarily into the ring of lymph nodes located along the junction of the head with the neck. These are the submental, submandibular, parotid/preauricular, retroauricular/mastoid, and suboccipital nodes. These groups of lymph nodes eventually drain into the deep cervical chains of lymph nodes.
Contraindications
No specific contraindications exist for scalp reconstruction. However, if the patient's underlying medical condition(s) prevent general anesthesia, this may limit the scope of the planned reconstruction. In rare patients, significant medical risk factors may prevent even the most limited reconstructions, including procedures that can be performed with the patient under local anesthesia. In these patients, strong consideration should be given to allowing the wound to heal by secondary intent. The surgeon's role in these situations is not so much to reconstruct the scalp but to coach it through the healing process with good wound care and conservative debridement of nonvital tissues when necessary.
Oishi SN, Luce EA. The difficult scalp and skull wound. Clin Plast Surg. Jan 1995;22(1):51-9. [Medline].
Baker SR, Johnson TM, Nelson BR. Technical aspects of prolonged scalp expansion. Arch Otolaryngol Head Neck Surg. Apr 1994;120(4):431-6. [Medline].
Azzolini A, Riberti C, Cavalca D. Skin expansion in head and neck reconstructive surgery. Plast Reconstr Surg. Nov 1992;90(5):799-807. [Medline].
Moelleken BR, Mathes SJ, Cann CE, Simmons DJ, Ghafoori G. Long-term effects of tissue expansion on cranial and skeletal bone development in neonatal miniature swine: clinical findings and histomorphometric correlates. Plast Reconstr Surg. Nov 1990;86(5):825-34. [Medline].
Calobrace MB, Downey SE. Calvarial deformity and remodeling following prolonged scalp expansion in a child. Ann Plast Surg. Aug 1997;39(2):186-9. [Medline].
Feierabend TC, Bindra RN. Injuries causing major loss of scalp. Plast Reconstr Surg. Aug 1985;76(2):189-94. [Medline].
Snow SN, Stiff MA, Bullen R, Mohs FE, Chao WH. Second-intention healing of exposed facial-scalp bone after Mohs surgery for skin cancer: review of ninety-one cases. J Am Acad Dermatol. Sep 1994;31(3 Pt 1):450-4. [Medline].
Kroll SS, Margolis R. Scalp flap rotation with primary donor site closure. Ann Plast Surg. May 1993;30(5):452-5. [Medline].
Ebihara H, Maruyama Y. Free abdominal flaps: variations in design and application to soft tissue defects of the head. J Reconstr Microsurg. Jul 1989;5(3):193-201. [Medline].
Borah GL, Hidalgo DA, Wey PD. Reconstruction of extensive scalp defects with rectus free flaps. Ann Plast Surg. Mar 1995;34(3):281-5; discussion 285-7. [Medline].
Borah GL, Chick LR. Island scalp flap for superior forehead reconstruction. Plast Reconstr Surg. Apr 1990;85(4):606-10. [Medline].
Chicarilli ZN, Ariyan S, Cuono CB. Single-stage repair of complex scalp and cranial defects with the free radial forearm flap. Plast Reconstr Surg. Apr 1986;77(4):577-85. [Medline].
Furnas H, Lineaweaver WC, Alpert BS, Buncke HJ. Scalp reconstruction by microvascular free tissue transfer. Ann Plast Surg. May 1990;24(5):431-44. [Medline].
Hallock GG. Long-term superiority of composite versus muscle-only free flaps for skull coverage. Ann Plast Surg. May 2004;52(5):507-10; discussion 510-1. [Medline].
Kobienia BJ, Migliori M, Schubert W. Preexpanded radial forearm free flap to the scalp. Ann Plast Surg. Dec 1996;37(6):629-32. [Medline].
Lai CS, Lin SD, Chou CK, Tsai CW. The subgalea-periosteal turnover flap for reconstruction of scalp defects. Ann Plast Surg. Mar 1993;30(3):267-71. [Medline].
Lee B, Bickel K, Levin S. Microsurgical reconstruction of extensive scalp defects. J Reconstr Microsurg. May 1999;15(4):255-62; discussion 263-4. [Medline].
Marathe US, Sniezek JC. Use of the vacuum-assisted closure device in enhancing closure of a massive skull defect. Laryngoscope. Jun 2004;114(6):961-4. [Medline].
McLean DH, Buncke HJ Jr. Autotransplant of omentum to a large scalp defect, with microsurgical revascularization. Plast Reconstr Surg. Mar 1972;49(3):268-74. [Medline].
Moore KL. The scalp. In: Clinically Oriented Anatomy. Philadelphia: Lipincott Williams & Wilkins; 1992:671-675.
Newman MI, Hanasono MM, Disa JJ, Cordeiro PG, Mehrara BJ. Scalp reconstruction: a 15-year experience. Ann Plast Surg. May 2004;52(5):501-6; discussion 506. [Medline].
Nordström RE, Devine JW. Scalp stretching with a tissue expander for closure of scalp defects. Plast Reconstr Surg. Apr 1985;75(4):578-81. [Medline].
Ozkan O, Coskunfirat OK, Ozgentas HE, Derin A. Rationale for reconstruction of large scalp defects using the anterolateral thigh flap: structural and aesthetic outcomes. J Reconstr Microsurg. Nov 2005;21(8):539-45. [Medline].
Sabapathy SR, Venkatramani H, Bharathi RR, D'Silva J. Technical considerations in replantation of total scalp avulsions. J Plast Reconst Aesth Surg. 2005;59:2-10.
Snow SN, Stiff MA, Bullen R, Mohs FE, Chao WH. Second-intention healing of exposed facial-scalp bone after Mohs surgery for skin cancer: review of ninety-one cases. J Am Acad Dermatol. Sep 1994;31(3 Pt 1):450-4. [Medline].
TerKonda RP, Sykes JM. Concepts in scalp and forehead reconstruction. Otolaryngol Clin North Am. Aug 1997;30(4):519-39. [Medline].
Ueda K, Harashina T, Inoue T, Tanaka I, Harada T. Microsurgical scalp and skull reconstruction using a serratus anterior myo-osseous flap. Ann Plast Surg. Jul 1993;31(1):10-4. [Medline].
Wang HT, Erdmann D, Olbrich KC, Friedman AH, Levin LS, Zenn MR. Free flap reconstruction of the scalp and calvaria of major neurosurgical resections in cancer patients: lessons learned closing large, difficult wounds of the dura and skull. Plast Reconstr Surg. Mar 2007;119(3):865-72. [Medline].
Serlett JM. Discussion--Management of a complex scalp defect. Plast Reconstr Surg. August, 2008;122(2):626-629.

