Sage Journals: Discover world-class research

Abstract

Cutis verticis gyrata (CVG) is characterized by extensive formation of scalp skin that mirrors the folds of the cerebral gyri. Giant CVG secondary to cerebriform intradermal nevus (CIN) has been rarely reported, and its management mainly involves surgical excision. In certain cases of giant CVG, however, surgical excision is dilemmatic. This case report describes a giant CVG secondary to CIN that was successfully managed with scalp expansion and surgical excision. Previously published studies are also reviewed.

Keywords

Cutis verticis gyrata cerebriform intradermal nevus scalp expansion surgery scalp reconstruction flaps

Introduction

Cutis verticis gyrata (CVG) is a rare congenital or acquired scalp disorder that manifests as scalp skin redundancy that mirrors the folds of the cerebral gyri. It was classified as primary (essential/nonessential) and secondary CVG by Polan and Butterworth.¹ CVG has a definite male predilection with an estimated prevalence of 1/100,000 in the male population and 0.026/100,000 in the female population.² Primary essential CVG is an extremely rare isolated and idiopathic condition, and primary nonessential CVG is associated with neuropsychiatric or ophthalmological disorders. Secondary CVG is more common and often occurs as a response to inflammatory or neoplastic processes. Cerebriform intradermal nevus (CIN) is an uncommon cause of secondary CVG, representing approximately 12.5% of all cases of CVG.³ Management requires surgical excision of the overlapping skin folds to provide a flat and smooth cosmetic appearance. Giant CVG secondary to CIN has been rarely reported, and surgical management is somewhat dilemmatic. The purpose of this case report is to present a case of giant CVG secondary to CIN in a 27-year-old woman that was successfully managed with surgical excision after scalp expansion and to review previous studies involving surgical management of CVG published in the literature.

Case report

A 27-year-old woman was admitted to the hospital for evaluation of a huge black scalp macule (20 × 18 cm) with thinning of the overlying hair (Figure 1). The asymptomatic scalp macule first appeared upon her birth and gradually increased in size. On physical examination, the scalp macule was characterized by brain-like sulcus and gyrus formation, which is a typical feature of CVG, without other abnormalities. Normal results were obtained for all laboratory tests, including routine blood, urine, and stool analyses; hepatorenal function; blood glucose and lipid concentrations; and electrolyte concentrations. The patient’s medical and familial histories were unremarkable. The patient was diagnosed with secondary CVG. Because tumoral lesions are the most common cause of secondary CVG and because of the aesthetic concerns associated with the disease, surgical management was considered the optimal treatment.

Figure 1.

(a) Occipital view of the cutis verticis gyrata (CVG) before scalp expansion, measuring 20 × 18 cm. (b) Lateral view of the CVG before scalp expansion.

We were concerned that the patient did not have enough hair-bearing tissue for scalp reconstruction after surgical excision because of the extensive scope of the lesion. Therefore, a two-stage surgery with reconstruction was finally planned. During the first stage, four rectangular inflatable tissue expanders (300-, 300-, 100-, and 80-mL) were placed under the scalp galea on both sides of the forehead and mastoid regions (Figure 2). Over a 6-month period, the expanders were inflated twice weekly until they reached a total volume of 1400, 1400, 450, and 400 mL, respectively. During the second stage, full-thickness excision of the lesion with a 0.5-cm skin margin was performed without disturbing the periosteum, and closure was achieved with rotation advancement flaps from the adjacent expanded scalp without perioperative complications (Figure 3). The patient was diagnosed with CIN according to postoperative pathological findings. During the 6-month postoperative follow-up, there was no evidence of recurrence; only a scar was present under the coverage of the hair.

Figure 2.

Four rectangular inflatable tissue expanders (300-, 300-, 100-, and 80-mL) were placed under the scalp galea on both sides of the forehead and mastoid regions and inflated twice weekly until they reached a total volume of 1400, 1400, 450, and 400 mL, respectively. (a) Occipital view of the cutis verticis gyrata (CVG) after scalp expansion. (b) Lateral view of the CVG after scalp expansion.

Figure 3.

(a) Occipital view of the operation area 1 month after excision. (b) Lateral view of the operation area 1 month after excision.

Discussion

As an uncommon cause of CVG, CIN typically presents as a slowly enlarging, asymmetric skin-colored macule of the parietal or occipital scalp with female predominance. The diagnosis is based on histopathologic findings.⁴ As its size increases, the lesion becomes more prominent and may exhibit separation by furrows, forming CVG. The management of giant CVG secondary to CIN is mainly surgical excision, not only for aesthetic and psychological reasons but also because of the 4.5% risk of malignancy transformation.⁵ Surgical management mainly involves excision and reconstruction using local flaps, free flaps, skin grafts, or scalp expansion according to the size of the lesion. Scalp reconstruction is deemed the most important concern.

The application of local flaps and skin grafts with different shapes and sizes is the traditional method of scalp reconstruction. Flaps and grafts can be used in most patients, but they cannot provide an optimal aesthetic outcome when the scalp defect after excision is extremely large. Moreover, the risk of relapse may increase when the excision is incomplete, and a second surgery might be required for complete correction. A free flap (e.g., a free latissimus dorsi musculocutaneous flap) is another feasible method of scalp reconstruction because of its large surface, long vascular pedicle, and reliably well-vascularized tissue. Similarly, serratus anterior, rectus abdominis, omental, and radial forearm flaps are also candidates during scalp reconstruction. Although a free flap reduces the number of operations and is an alternative in patients with a large scalp defect after excision or without enough hair-bearing tissue for reconstruction, use of such a flap can result in an unaesthetic hairless region in the surgical area and scar formation at the donor site, resulting in an unsatisfactory cosmetic appearance. Scalp expansion provides optimal aesthetic and functional outcomes with maximum efficiency by expanding the remaining parts of the scalp, making the scalp flap design during surgery simple and flexible. For reconstruction of large scalp defects, the most appropriate donor remains the scalp itself, which makes scalp expansion the optimal treatment option for giant CVG.

All cases of surgically managed CVG published in the literature according to our PubMed search are listed in Table 1.^2,4,6–24 Thirty-five patients (11 female, 24 male; mean age, 26.9 years) with CVG (maximum lesion diameter, 8–32 cm) were successfully treated with scalp excision followed by direct suturing (n = 9), scalp subcision (n = 1), local flaps (n = 2), free flaps (n = 2), skin grafts (n = 3), and scalp expansion (n = 18). Various excision patterns have been reported, such as a Y-shaped excision, T-shaped excision, fleur-de-lis pattern, and butterfly-shaped excision. Scalp reconstruction with local flaps and skin grafts has mainly been used in patients with relatively small scalp defects; the largest reported defect was 20 × 15 cm. For giant CVG with an expected large resultant scalp defect, a free flap is an alternative and scalp expansion is the favorable option, with a reported maximum corrected scalp defect of 32 × 27 cm.

Table 1.

Cutis verticis gyrate managed with surgical options published in the literature.

Authors	Year	Cases	Sex	Age	Diagnosis	Lesion size	Management
Abu-Jamra and Dimick⁶	1966	1	Male	49	CVG	NA	Y-shaped excision followed by direct suturing
Garden and Robinson⁷	1984	1	Male	26	Primary essential CVG	9 cm in diameter	Y-shaped excision followed by direct suturing
Jeanfils et al.⁸	1993	1	Male	43	Secondary CVG due to CIN	32 × 27 cm	Scalp excision followed by primary closure with three left-leg flaps and then scalp expansion followed by extended excision
Hashimoto et al.⁹	1999	1	Female	7	Secondary CVG due to CIN	12 × 14 cm	Scalp expansion followed by excision
Snyder et al.²	2002	1	Female	1.5	Primary CVG with Turner syndrome	5 × 8 cm	Scalp expansion followed by excision
Al-Malaq et al.¹⁰	2002	3	Male	Mean, 30	Primary CVG	NA	Scalp excision followed by direct suturing
Zhao et al.¹¹	2006	1	Female	20	Primary CVG	22 × 16 × 2.5 cm	Scalp expansion followed by excision
Wang et al.¹²	2007	6	5 Male and 1 female	17–58; mean, 29.8	CVG	Minimum 8 × 6 cm, maximum 24 × 18 cm	Four scalp expansions followed by excision and two scalp excisions followed by primary closure with skin graft
Misirlioglu et al.¹³	2008	1	Female	46	Primary CVG	10 × 12 cm	Scalp excision followed by primary closure with pinwheel flaps
Radwanski et al.¹⁴	2009	1	Male	30	Primary essential CVG	NA	Fleur-de-lis–shaped excision followed by direct suturing
Hsu et al.¹⁵	2009	1	Male	37	Primary essential CVG	Seven sagittal gyri	Scalp subcision
Mishra et al.¹⁶	2010	1	Female	18	CVG	80% of scalp	Scalp expansion followed by excision
Dumas et al.¹⁷	2010	1	Male	18	Primary essential CVG	NA	T-shaped excision followed by direct suturing
Zhang et al.⁴	2011	1	Female	17	Secondary CVG due to CIN	30 × 22 × 3 cm	Scalp expansion followed by excision
Tagore and Ramineni¹⁹	2011	1	Male	14	Secondary CVG due to CIN	20 × 15 cm	Scalp excision followed by primary closure with skin graft
Zhao et al.¹⁸	2012	8	6 Male and 2 female	17–56; mean, 31	CVG	Minimum 3 × 8 cm, maximum 9 × 15 cm	Scalp expansion followed by excision
Taha and Orlando²⁰	2014	1	Male	28	Primary essential CVG	NA	Butterfly-shaped excision followed by direct suturing
Mutlu et al.²¹	2016	1	Male	18	Secondary CVG due to CIN	80% of scalp	Scalp excision followed by primary closure with free latissimus dorsi musculocutaneous flap
Sahni et al.²²	2016	1	Female	13	Secondary CVG due to CIN	12 × 14 cm	Scalp expansion followed by excision
Lamelas et al.²³	2016	1	Male	1.9	Primary essential CVG	NA	Scalp excision followed by primary closure with multiple adjacent Z-plasties
Ennouhi et al.²⁴	2018	1	Female	36	Primary essential CVG	15 × 6 cm	Elliptical excision followed by direct suturing

CVG, cutis verticis gyrate; CIN, cerebriform intradermal nevus; NA, not available.

Conclusion

Giant CVG secondary to CIN may be excised with scalp expansion in patients without enough hair-bearing tissue for scalp reconstruction.

Footnotes

Acknowledgement

We would like to thank the patient for providing consent for publication of this case.

Declaration of conflicting interest

The authors declare that there is no conflict of interest.

Ethical approval

All procedures involving this patient were performed in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Funding

This work was supported by the CAMS Innovation Fund for Medical Sciences (Grant No. CAMS-12M-1-007).

Informed consent

Informed consent was obtained from the patient described in this report.

ORCID iD

Wenfang Dong

References

Polan

Butterworth

Cutis verticis gyrata; a review with report of seven new cases. Am J Ment Defic 1953; 57: 613–631.

Snyder

Johnson

Hollins

RR.

Congenital primary cutis verticis gyrata.

Plast Reconstr Surg 2002; 110: 818–821.

Orkin

Frichot

3rd Zelickson

AS.

Cerebriform intradermal nevus. A cause of cutis verticis gyrata. Arch Dermatol 1974; 110: 575–582.

Zhang

Sun

Liu

, et al. Rare giant secondary cutis verticis gyrata. J Plast Surg Hand Surg 2011; 45: 212–214.

Hayashi

Tanioka

Taki

, et al. Malignant melanoma derived from cerebriform intradermal naevus. Clin Exp Dermatol 2009; 34: e840–e842.

Abu-Jamra

Dimick

DF.

Cutis verticis gyrata. A report of a case secondary to acromegaly treated with plastic surgery and x-ray therapy.

Am J Surg 1966; 111: 274–277.

Garden

Robinson

JK.

Essential primary cutis verticis gyrata. Treatment with the scalp reduction procedure.

Arch Dermatol 1984; 120: 1480–1483.

Jeanfils

Tennstedt

Lachapelle

JM.

Cerebriform intradermal nevus. A clinical pattern resembling cutis verticis gyrata.

Dermatology 1993; 186: 294–297.

Hashimoto

Urano

Nakanishi

, et al. Cerebriform intradermal nevus: a case of scalp expansion on the galea. J Dermatol 1999; 26: 258–263.

10.

Al-Malaq

Hashem

Helmi

, et al. Surgical correction of primary cutis vertices gyrata. Ann Plast Surg 2002; 49: 673–675.

11.

Zhao

Fang

, et al. Giant primary cutis verticis gyrata successfully treated with surgical excision and tissue expansion. Dermatol Surg 2006; 32: 753–755.

12.

Wang

Chu

Shui

, et al. [Cutis verticis gyrata]. Zhonghua Zheng Xing Wai Ke Za Zhi 2007; 23: 112–114.

13.

Misirlioglu

Karaca

Akoz

Primary cutis verticis gyrata and scalp reduction in one stage with multiple pinwheel flaps (revisited). Dermatol Surg 2008; 34: 935–938.

14.

Radwanski

Almeida

Pitanguy

Primary essential cutis verticis gyrata–a case report.

J Plast Reconstr Aesthet Surg 2009; 62: e430–e433.

15.

Hsu

Chang

, et al. Using novel subcision technique for the treatment of primary essential cutis verticis gyrata. Int J Dermatol 2009; 48: 307–309.

16.

Mishra

Tehrani

Hancock

, et al. Management of primary cutis verticis gyrata with tissue expansion and hairline lowering foreheadplasty. J Plast Reconstr Aesthet Surg 2010; 63: 1060–1061.

17.

Dumas

Medard De Chardon

Balaguer

, et al. [Primary essential cutis verticis gyrata: case report and literature review]. Ann Chir Plast Esthet 2010; 55: 243–248.

18.

Zhao

Wang

, et al. Treating cutis verticis gyrata using skin expansion method. Cell Biochem Biophys 2012; 62: 373–376.

19.

Tagore

Ramineni

AK.

A case of cutis verticis gyrata secondary to giant cerebriform intradermal nevus. Indian J Pathol Microbiol 2011; 54: 624–625.

20.

Taha

Orlando

Butterfly-shape scalp excision: a single stage surgical technique for cutis verticis gyrata.

J Plast Reconstr Aesthet Surg 2014; 67: 1747–1749.

21.

Mutlu

Colak

Canli

, et al. Scalp reconstruction with free latissimus dorsi flap in a patient with giant cutis verticis gyrata. J Craniofac Surg 2016; 27: e553–e554.

22.

Sahni

Singh

Bhari

, et al. Giant cerebriform intradermal nevus in a young girl. Indian Dermatol Online J 2016; 7: 443–444.

23.

Lamelas

Taub

Silver

, et al. Congenital primary essential cutis verticis gyrata. Eplasty 2016; 16: ic13.

24.

Ennouhi

Guerrouani

Moussaoui

Idiopathic cutis verticis gyrata in a female. Cureus 2018; 10: e2105.