INTRODUCTION
The outer table of the calvarium receives nutrition through the periosteum. Large
scalp defects owing to trauma or neoplasms can endanger the vitality of the bones
of the neurocranium, dura mater, and underlying brain. The loose connective tissue
between aponeurotic galea/epicranium muscle and periosteum favors intracranial metastases,
thrombi, and infections1.
Large scalp defects are a major challenge for reconstruction, and in the absence of
periosteum, these impair the use of skin grafts. Decortication of the outer table
for skin grafting of the diploe provides aesthetically poor results, leading to fragility
and susceptibility to malignancy. Romero et al., in 20182, published an algorithm recommending microsurgery for defects larger than 5 cm. Although
vascular microsurgery provides the best results in the repair of large scalp defects3, it requires adequate team and resources. Souza, in 20124, used local flaps and emphasized the importance of superficial temporal vessels in
maintaining the viability of these flaps.
CASE REPORTS
CASE 1
A 69-year-old male patient with hypertension and diabetes underwent kidney transplant
17 years ago and regularly uses immunosuppressants. He had actinic keratoses on the
face, scalp, and limbs, which were treated with cryotherapy and fluorouracil. In 2015,
he had large moderately differentiated squamous cell carcinoma (SCC) with muscle invasion
in the dorsum of the nose and was treated by excision and coverage using midline forehead
flap. He had multiple and recurrent moderately differentiated multifocal SCC in the
parietal regions (Figure 1).
Figure 1 - A: (Case 1) Recurrent squamous cell carcinomas in a renal transplant patient and defects
after excision. B: (Case 1) Intraoperative period showing the anterior flap with later distal epidermolysis.
C: (Case 1) Late postoperative appearance.
Figure 1 - A: (Case 1) Recurrent squamous cell carcinomas in a renal transplant patient and defects
after excision. B: (Case 1) Intraoperative period showing the anterior flap with later distal epidermolysis.
C: (Case 1) Late postoperative appearance.
CASE 2
A 68-year-old male, white patient with diabetes and rheumatoid arthritis regularly
uses corticosteroids and methotrexate. He had multiple actinic keratoses on the bald
scalp and was initially treated with cryotherapy. After 4 years, he returned with
a recent, rapid-growth, infiltrate, vegetative, painful, ulcerated lesion in the frontoparietal
region of the scalp measuring 4.5 x 4.0 x 1.5 cm. A biopsy revealed a well-differentiated,
ulcerated SCC extending up to the hypodermis (Figure 2).
Figure 2 - A: (Case 2) Vegetating squamous cell carcinoma in an immunosuppressed patient and the
defect after excision. B: (Case 2) Transoperative appearance: flap rotation and final aspect. C: (Case 2) Late postoperative appearance.
Figure 2 - A: (Case 2) Vegetating squamous cell carcinoma in an immunosuppressed patient and the
defect after excision. B: (Case 2) Transoperative appearance: flap rotation and final aspect. C: (Case 2) Late postoperative appearance.
CASE 3
A 68-year-old male patient who underwent a liver transplant nine years ago and continuously
uses immunosuppressants. He had a large vegetative lesion in the left parieto-occipital
region. A biopsy revealed exophytic SCC (Figure 3).
Figure 3 - (Case 3) Squamous cell carcinoma in a renal transplant patient: initial lesion, deformity
after excision, flap rotation, and final appearance.
Figure 3 - (Case 3) Squamous cell carcinoma in a renal transplant patient: initial lesion, deformity
after excision, flap rotation, and final appearance.
CASE 4
An adult male patient who was struck with an ax seven years ago suffered head trauma.
He was operated four times at Neurosurgery Services. For more than once, cranioplasty
was performed with self-polymerizing acrylic, followed by subsequent infection and
frontoparietal osteomyelitis, requiring the removal of the implant and new bone debridement
(Figure 4).
Figure 4 - (Case 4) Sequelae of head trauma: frontoparietal bone loss with skin graft over the
dura mater and fistula. Tissue expansion, cranioplasty, and immediate and late postoperative
period.
Figure 4 - (Case 4) Sequelae of head trauma: frontoparietal bone loss with skin graft over the
dura mater and fistula. Tissue expansion, cranioplasty, and immediate and late postoperative
period.
At another service, he received partial skin graft placed directly on the remaining
dura mater and the presumably performed galeal flap. Initial examinations revealed
a frontoparietal defect, subdural clamps, and a clinically significant fistula draining
serous material over the brain mass precariously protected by the graft. He had convulsive
episodes after suffering minor trauma in the graft region during his work as a car
mechanic.
DISCUSSION
The low elasticity, thickness of the skin and subcutaneous tissue, and presence of
a thick aponeurotic galea on a convex surface make the reconstruction of large scalp
defects a challenging task. Abundant anastomoses between the temporal, supraorbital,
supratrochlear, posterior auricular and occipital vessels usually allow scalp flaps
with only a small pedicle to survive and large flaps to recover without complications5,6.
Most published cases of SCC have reported occurrence in the head and neck, with 8.3%–25.2%
lesions occurring in the scalp. The current large numbers of living patients who underwent
transplantation require more attention since immunosuppressants contribute to the
formation of skin neoplasms.
The clinical recommendation for the margin of excision of SCC is 4 mm for low-risk
patients and 6 mm for high-risk patients7. We use about 10 mm of margin based on the pathology, frequently removing the periosteum.
In case 1, local relapses and coalescence of premalignant lesions required a large
excision. Although the large defect (16 x 16 cm) indicated the need for a microsurgical
free flap, the chronic use of immunosuppressants, diabetes, and hypertension increases
the risk of compromising the kidney transplanted 17 years ago in a longer surgery.
We used two temporal-parietal-occipital rotation flaps for the reconstruction. The
first, with a pedicle in the right temporal region, was rotated to cover the earliest
portion of the defect. The second, lower and longer, with pedicle in the left temporal
region, was rotated to occlude the posterior portion. The secondary occipital defect,
with intact periosteum, received an inguinal total skin graft. In the postoperative
period, epidermolysis and superficial necrosis occurred on the distal margin of the
first flap. They were treated by debridement with hyaluronidase and outpatient cleaning,
followed by dressings with Rifamycin and, finally, by colloidal occlusive dressings,
showing excellent results.
Chronic use of methotrexate in patients with severe rheumatoid arthritis causes immunosuppression
(case 2). After excision of the lesion, two randomized flaps were used: one larger
and longer on the right with occipital pedicle, and one smaller on the left with temporal
pedicle.
Distal suffering occurred in the flap on the right, leading to bone exposure and gap.
With local anesthesia, a small flap of adjacent galea was rotated and sutured over
the exposed bone. Using occlusive hydrocolloid dressings, epithelialization from the
galea completely repaired the defect. This case illustrates the high safety of the
pediculated flap in the temporal vessels and the high epithelization capacity of the
galea.
Case 3, who underwent liver transplantation, received surgical treatment similar to
case 2. But in this case, the right flap of the occipital pedicle was shorter, and
there were no complications.
In case 4, temporal, frontal, and occipital scars limited the use of flaps. Tissue
expansion was the option chosen in the absence of microsurgical resources in a local
public hospital in the 1980s. This technique was recommended by Sasaki in 19858, Anger in 19889, and other authors10, followed by cranioplasty Korloff et al., 197311 and some osteosyntheses with steel wires. Despite the extrusion of one synthesis
and a small bone fragment, it had no relapse of the fistula, with adequate protection
to the brain and excellent aesthetic results. This case illustrates the use of an
expanded advancement flap in the unpredictability of temporal flaps.
CONCLUSION
The experience gained in the surgical treatment of these complex and unusual cases
indicates the preferred choice of random-pattern large fasciocutaneous flaps with
temporal pedicles in the reconstruction of large scalp defects over microsurgery.
Distal ischemic suffering may occur in these flaps, but when they are adequately treated,
as in the cases presented, excellent aesthetic and functional results are achieved.
COLLABORATIONS
JWF
|
Analysis and/or data interpretation, Conception and design study, Conceptualization,
Data Curation, Final manuscript approval, Investigation, Methodology, Project Administration,
Realization of operations and/or trials, Supervision, Validation, Visualization, Writing
- Original Draft Preparation, Writing - Review & Editing
|
KSMP
|
Data Curation, Investigation, Realization of operations and/or trials, Writing - Original
Draft Preparation, Writing - Review & Editing
|
MHM
|
Writing - Original Draft Preparation, Writing - Review & Editing
|
REFERENCES
1. Jr CCC. Tumors involving the craniofacial skeleton. In: McCarthy JG, ed. Reconstructive
plastic surgery: tumors head neck. Philadelphia: WB Saunders Company; 1977. p. 2757-75.
2. Romero RM, Arikat A, Machado Filho G, Aita CD, Oliveira MP, Jaeger MRO. Reconstrução
de defeitos no couro cabeludo. Rev Bras Cir Plást. 2018;33:90-2.
3. Steiner D, Horch RE, Eyüpoglu I, Buchfelder M, Arkudas A, Schmitz M, et al. Reconstruction
of composite defects of the scalp and neurocranium — a treatment algorithm from local
flaps to combined AV loop free flap reconstruction. World J Surg Oncol. 2018;16:217.
4. Souza CD. Reconstrução de grandes defeitos de couro cabeludo e fronte em oncologia:
tática pessoal e experiência – análise de 25 casos. Rev Bras Cir Plást. 2012;27(2):227-37.
5. Marchac D. Deformities of the forehead, scalp, and cranial vault. In: McCarthy JG,
ed. Plastic surgery. Philadelphia: WB Saunders Company; 1990. p. 1538-73.
6. Bradford BD, Lee JW. Reconstruction of the forehead and scalp. Facial Plast Surg Clin
North Am. 2019:27(1):85-94.
7. Jenkins G, Smith AB, Kanatas AN, Houghton DR, Telfer MR. Anatomical restrictions in
the surgical excision of scalp squamous cell carcinomas: does this affect local recurrence
and regional nodal metastases? Int J Oral Maxillofac Surg. 2014:43(2):142-6.
8. Sasaki GH. Tissue expansion. São Paulo: Dow Corning Healthcare Centre; 1985.
9. Anger J. Expansão de tecidos. São Paulo: Dow Corning do Brasil; 1988.
10. Fernandes JW. Expansores de pele. In: Fernandes JW, org. Cirurgia plástica - Bases
e refinamentos. Curitiba: Primax; 2012. p. 159-70.
11. Korloff B, Nylen B, Rletz K. Bone grafting of skull defects. Plast Reconstr Surg.1973;
52:378-383
1. Universidade Positivo, Curitiba, PR, Brazil.
2. Faculdade Evangélica Mackenzie do Paraná, Curitiba, PR, Brazil.
Corresponding author: Julio Wilson Fernandes Avenida Getúlio Vargas, 2079, Curitiba, PR, Brazil. Zip Code: 80250-180. E-mail:
: cirurgiaplasticajwf@uol.com.br
Article received: June 7, 2019.
Article accepted: February 29, 2020.
Conflicts of interest: none.