Trichilemmal cyst is sometimes seen in the scalp of adults. We herein describe a rare case of a trichilemmal cyst arising on the forehead of a child.

A 9-year-old boy visited our hospital, complaining of a nodule above the left eyebrow that had increased in size over the previous year. He had no past medical history, and he and his parents denied any prior triggering events such as trauma on this site. Physical examination showed a 7×5mm, normal skin-colored, slightly dome-shaped subcutaneous nodule (Fig. 1). Laboratory examination was normal. The nodule was surgically removed under local anesthesia. Histopathological examination revealed a relatively well-circumscribed cystic structure located in the subcutaneous tissue (Fig. 2A). The cyst was filled with acidophilic amorphous substances, and the cyst walls consisted of epithelial cells without forming granular cell layers (Fig. 2B). The serial sections of histopathology showed cholesterin crystals and foreign body giant cells within and around the cyst (Fig. 2C). After the surgery was performed, 10 years have passed without local recurrence.

Figure 1.

A slightly dome-shaped subcutaneous nodule above the left eyebrow (arrow).

(0.15MB).

Figure 2.

(A) Histopathological examination showing a cystic structure located in the subcutaneous tissue (Hematoxylin & eosin, ×20). (B) Higher magnification shows that the cyst walls keratinize towards the lumen without forming granular cell layers (Hematoxylin & eosin, ×200). (c) Cholesterin crystals and foreign body giant cells (Hematoxylin & eosin, ×200).

(0.87MB).

We diagnosed the case as a trichilemmal cyst based on the histopathological features of well-defined cystic structures consisting of epithelial cells showing trichilemmal keratinization. Cholesterin crystals and cholesterin clefts, which are often observed in epidermal cysts, were observed in the present case, but those histopathological features are not diagnostic. The presence of foreign body granuloma may suggest previous partial ruptures of trichilemmal cysts. The cyst wall was not adjacent to sebaceous glands, and hair follicles and hair shafts were not observed in and around the cysts. Moreover, the subcutaneous nodule did not exist at birth, and thus dermoid cyst was excluded. Trichilemmal cyst is a benign adnexal tumor that arises from the outer root sheath of a hair follicle. It usually presents as an asymptomatic firm nodule, which at times can be slightly painful. It is mainly seen in areas bearing hair follicles, mostly on the scalp. Middle-aged females are more commonly affected.1 The onset of a trichilemmal cyst in a young boy is rare. To our knowledge, only 3 cases have been reported which developed trichilemmal cysts under the age of 10, including the present case.2,3 Clinical findings of these cases are shown in Table 1. The thigh, penis, and eyebrow were involved, which were rare sites. Our patient in the current case is now the youngest among the reported Japanese cases. On the other hand, the youngest case was in a 5-year-old male, who developed a trichilemmal cyst on the penis after hypospadias repair.3 The authors speculated that the distal hypospadias repair had triggered squamous metaplasia with keratinization, leading to the development of a trichilemmal cyst in a non-hair-bearing area of the body.

In our department, 25 cases including the present case were diagnosed as trichilemmal cysts over the past 10 years. The pediatric case was only 1 (the present case). The patients consisted of 12 males and 13 females, and the mean age was 49 years. The involved sites were most frequently observed in the scalp (n=16), followed by the face (7), abdomen (1) and forearm (1). Among the facial lesions, 2 were observed in the eyebrow, 2 were observed in the upper and lower eyelids, 2 were observed in the forehead, and 1 was observed in the cheek. Trichilemmal cyst is one of the nodules arising on the head and neck, which rarely involves the children.