Dear Editor:
A 54-year-old male presented with multiple nodules on the scrotum which lasted for 2 years. The lesions were distributed together on the right side of the scrotum (Fig. 1A). A punch biopsy was conducted on the scrotal nodule. Histological findings showed only keratin materials. After a month, the surgery was performed under local anesthesia. Multiple scrotal nodules, including part of the dartos muscles, were removed at once (Fig. 1B). Then, the defect site was repaired using an advancement flap with dartos muscle. Histological findings of the removed lesions showed several epidermal cysts.
Fig. 1. Clinical photographs of clinical features. (A) Multiple nodules were placed on the right side of the scrotum. (B) Scrotum with multiple scrotal nodules, including the dartos muscle resected in a single resection. We received the patient’s consent form about publishing all photographic materials.
Epidermal cysts are well encapsulated, and histologically characterized by a lining of stratified squamous cells. Cysts that occur in the scrotum could often be left unnoticed, because they have no symptoms. However, if an infection occurs especially in multiple cysts, the infection could spread to the surrounding cysts and rarely, the whole scrotal wall. This can lead to serious complications, including Fournier’s gangrene and septicemia1. This is why it is important to treat multiple cysts of the scrotum through complete excision.
Multiple nodules on the scrotum could have several different diagnoses, including idiopathic scrotal calcinosis (ISC), steatocystoma multiplex, or milia en plaque (MEP). However, the most common misdiagnosis of scrotal cysts is ISC. It is a rare benign condition, which is termed as such due to the abnormal deposition of calcium in the scrotal skin or subcutaneous tissue. In the case of ISC, histological findings are characterized by the deposition of calcium in the dermis without an epithelial lining. Some authors suggest that ISC is actually a misnomer and its underlying cause is the calcification of the epidermal cyst of the scrotum2. The characteristics of the differential diagnosis of epidermal cyst en plaque are summarized in a Table 12,3,4.
Table 1. Differential diagnoses of epidermal cyst en plaque.
Contents | Epidermal cyst | MEP3 | Idiopathic calcinosis cutis2 | Steatocystoma multiplex4 |
---|---|---|---|---|
Peak age | Third and fourth decades | Fourth to seventh decades | Third and fourth decades | Second and third decades |
Clinical features | Flesh colored nodule | Firm, white papules (several millimeters) on an erythematous base | Slow-growing yellowish nodules | Firm, yellowish colored papules and nodules |
Histology | Lined by stratified squamous cells with keratinous and other materials | Lined by stratified squamous cells with keratinous materials | Deposition of calcium in the dermis without lining | Lined by stratified squamous epithelium containing sebaceous gland |
Predilection site | Scalp, Trunk, Face | Retroauricular area | Scrotum | Chest |
Lesion numbers | Single to multiple | Multiple | Single to multiple | Multiple |
Treatment options | Excision | Excision Topical retinoids |
Excision | Excision Laser treatment |
MEP: milia en plaque.
In this case, the patient was treated with a single-stage excision and reconstruction and he was satisfied cosmetically and functionally. There are several reasons why this treatment was possible. First, the lax nature of the scrotum and abundant tissue of scrotal skin ensured that only minimal defects were left after reconstruction. And because the scrotum receives blood supply by multiple vascular systems which run through the fascia of dartos muscle, the risk of ischemia, which is important for flap design, is low5. In addition, the patient had multiple nodules in one plaque. Considering that the distribution of these lesions is similar to that seen in MEP3, it was named epidermal cyst en plaque. It is believed that this rare en plaque distribution of lesions helped to perform a complete excision. In literature, a form of concentrated distribution of epidermal cysts in a limited part of the scrotum, as in this case, has not yet been reported.
In conclusion, we report a rare case of epidermal cyst en plaque of scrotum. The fact that it occurred in the elastic scrotal skin and the characteristic distribution of the lesion facilitated a complete excision and reconstruction of the lesion with minimal defects.
Footnotes
CONFLICTS OF INTEREST: The authors have nothing to disclose.
FUNDING SOURCE: None.
References
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