Archives of Medicine and Health Sciences

CASE REPORT
Year
: 2013  |  Volume : 1  |  Issue : 2  |  Page : 152--154

Giant bathing trunk nevus in a child: Case report with review of literature


Sonia Jain 
 Department of Skin and V. D., Mahatma Gandhi Institute of Medical Sciences, Sewagram, Wardha, Maharashtra, India

Correspondence Address:
Sonia Jain
A-14, Dhanvantri Nagar, MGIMS, Sewagram, Wardha - 442 102, Maharashtra
India

Abstract

Giant pigmented nevi are congenital melanocytic nevi that are of great cosmetic distress for the patient and cause an equal psychological stress to the parents. Here we report a case of a 4 year old female child who presented to us with a large black patch over her back extending upto upper half of her buttocks with multiple satellite lesions all over the body, since her birth. Their management is a challenge for the treating dermatologist owing to their large size and a propensity to recur. There have been reports of malignant change in upto 2% to 15% of the cases. However, there have been recent advances in the field with many new therapeutic modalities available.



How to cite this article:
Jain S. Giant bathing trunk nevus in a child: Case report with review of literature.Arch Med Health Sci 2013;1:152-154


How to cite this URL:
Jain S. Giant bathing trunk nevus in a child: Case report with review of literature. Arch Med Health Sci [serial online] 2013 [cited 2020 Apr 6 ];1:152-154
Available from: http://www.amhsjournal.org/text.asp?2013/1/2/152/123031


Full Text

 Introduction



Giant congenital melanocytic nevi, also known as 'bathing trunk nevi' or 'garment nevi,'[1] are large macular lesions with diameters over 20 cm that are present since birth and develop coarse terminal hair over a period of years. [2] One to three percent of the newborns have melanocytic nevi at birth. Nevi have been arbitrarily divided into small, intermediate, and giant varieties depending on the size of the lesions, i.e., less than 1.5 cm, 1.5 cm to 20 cm, and more than 20 cm, respectively. [3] The life time risk of malignant transformation in a giant melanocytic nevus ranges from two to 31 percent with an average of 12% as reported by Kopf et al. (1979).

 Case Report



Here, we report the case of a 4-year-old girl who presented to us with an extensive black pigmented lesion of her trunk extending up to her buttocks [Figure 1] and [Figure 2]. She had similar small black patches over both upper and lower extremities and over her cheeks with a prominent hair growth over the area [Figure 3] and [Figure 4]. She had the pigmentation over her body right from her birth. She did not give any history of seizures or focal neurological deficit. She had no associated systemic or mucosal anomalies. She was younger of the two siblings, and none of her family members had similar complaints, and neither was there a family history of consanguineous marriage. Her detailed skin and mucosal examination did not reveal any ulceration or bleeding from the lesions. On history and clinical examination, there were no signs and symptoms of neurological involvement. A CT scan of the head did not show any deep CNS extension. Fundus examination, ultrasound of the abdomen, and an X-ray of the spine were normal. The biopsy of the patient was taken, and the histopathological findings were consistent with those of congenital melanocytic nevi without any evidence of a malignant transformation in the biopsied lesion.

Other common associated congenital abnormalities like spina bifida, meningocoele, club foot, hypertrophy or atrophy of a limb involved by the nevus, hamartomas such as vascular nevi, lipomas, or von Recklinghausen's disease were not found. She was advised a regular clinical follow-up to detect any malignant transformation at the earliest, if any.{Figure 1}{Figure 2}{Figure 3}{Figure 4}

 Discussion



Bathing trunk nevi are caused by defects that occur as the fetus grows in utero. However, in some families, they are known to be inherited. A bathing trunk nevus may occur with lipomas, neurofibromatosis, other nevi, and spina bifida. [4] There are two main problems faced in managing these giant nevi, one being their potential for malignant change resulting in need for prophylactic removal, [5] and other being the cosmetic concern to the patient. Histopathologically, three patterns may be encountered: A compound or an intra-dermal nevus, a neural nevus, and a blue nevus pattern. [6] The epidermis shows the presence of nevomelanocytes, which, however, may be seen to the mid and the deep dermis as well in the form of sheets, nests, cords giving the characteristic 'Indian file' appearance. [7] They invade the appendageal and the neurovascular structures as well. Unique to the giant congenital nevi is the occasional presence of nevomelanocytes within the substance of the muscle, bone, placenta, umbilical cord, cranium, and dura mater. [8]

As already mentioned, managing giant nevi is a challenging task. The literature does not show any satisfactory form of treatment for congenital nevus of such dimensions. However, with many recent modalities of treatment available, there is now a ray of hope for those affected. Prior to any active intervention planned in this regard whatsoever, it is very prudent to get a biopsy and an MRI (Magnetic resonance imaging) done for two most important reasons. Firstly, to rule out neurocutaneous melanosis, which, if present, may decrease the very need to remove the bulk of the skin lesions as the neural component would still remain inaccessible. Secondly, to rule out the real chance of underlying spinal dysraphism. The various options available include staged excision with tissue expansion or grafting, dermabrasion, [9] curettage, Q switch Ruby laser [1] or erbium: YAG laser. We had to refer the patient to higher center for further management.

References

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