Case report – ancient schwannoma of the scrotum
© Chan et al; licensee BioMed Central Ltd. 2007
Received: 22 September 2006
Accepted: 23 January 2007
Published: 23 January 2007
Scrotal schwannoma is a rare neoplasm and poses a diagnostic challenge to urologists. This article describes a rare case of ancient scrotal schwannoma and reviews the current modality of investigation and treatment of this tumour.
A 28 year old man presented with a 3-month history of an asymptomatic scrotal swelling. Ultrasonography and computer topography revealed an intra-scrotal and extra-testicular mass without local invasion. Surgical excision was undertaken and histology was an ancient schwannoma of the scrotum.
Schwannoma is a benign encapsulating neoplasm with an overall low incidence, occurring mostly in the head and neck region and seldom in the scrotum. Histology shows two distinctive patterns, Antoni type A and B areas. Variations of schwannoma such as cellular, ancient, glandular and epithelioid are observed based on the appearances. Ancient schwannoma exhibits pleomorphism without mitosis as the result of cellular degeneration, which can lead to an erroneous diagnosis of malignancy. Imaging modalities are non-specific for schwannomas, but can define tumour size, site and extension. The mainstay treatment is complete excision, although local recurrence may occur in large and incompletely excised lesions. Malignant change is exceedingly rare.
The "ancient" variant of schwannomas is a rare subtype of a benign encapsulated neoplasm of the nerve sheath . A review of current literature has revealed several reported sites but not in the scrotum. Here we report such a scrotal tumour arising in a 28-year old man, paying particular attention to the potential diagnostic difficulties prior to surgical intervention.
A 28-year old man presented with a three month history of an asymptomatic scrotal swelling. He had previously undergone orchidopexy in childhood for a mal-descended right testis. There is otherwise no other significant medical or family history. The mid-scrotally located mass measured 4 × 7 cm and was nodular, hard and clinically separate from the testes. It was not attached to the scrotal skin or other underlying structures. Lymphadenopathy was not detected.
An initial diagnostic wedge biopsy indicated the lesion could be an ancient schwannoma. Curative surgical excision with partial scrotectomy was undertaken for removal of the mass and for definitive diagnosis. At resection, the tumour appeared to be superficial to the tunica vaginalis, testes and corpus spongiosum. Inferiorly, the tumour was attached to the bulbospongiosus requiring partial resection of the superficial muscle fibres.
A schwannoma is a benign encapsulated neoplasm derived from schwann cells of the nerve sheath. The exact incidence of schwannomas is unknown, but they are rare. Schwannomas are found in all age groups but are more common in the first four decades and affect both sexes equally. They may occur in association with neurofibromatosis or arise sporadically. The microscopic appearance of schwannoma is distinctive , with two recognisable patterns. Antoni A areas are composed of compacted spindle cells often arranged in palisades or in an organoid arrangement (Verocay bodies). Antoni B areas consist of tumour cells suspended in a myxomatous matrix that may appear microcystic. Several variants of schwannomas based on appearances have been observed, including cellular, glandular, epithelioid and ancient types, and all exhibit benign progression. Cellular schwannomas are almost exclusively composed of Antoni A areas but lack Verocay bodies. The glandular and epitheloid variants compose of epitheloid areas and glandular component, respectively, to acquire their descriptive names. Ancient schwannomas show bizarre hyperchromatic nuclei without mitoses. To the unwary, these features can lead to an erroneous diagnosis of malignancy, although the very low mitotic activity should allow these tumours to be distinguished from malignant nerve sheath tumours.
A literature review showed that whilst ancient schwannomas are rare, most cases occur in the head and neck region  (trigeminal nerve, facial nerve, vestibular nerve, vagus nerve, parotid, thyroid, vocal cord, floor of mouth, orbit and infra-temporal fossa). Other less common sites include the extremities, mediastinum, thorax , retroperitoneum , pancreas  and pelvis . Scrotal schwannomas have been infrequently described in the medical literature [7, 8, 10], however, we could not find references pertaining to the ancient variant in the scrotal region.
Schwannomas pose a difficult diagnostic challenge to urologists. Radiological findings are often non-specific . Ultrasonography can differentiate between solid and cystic tumours. CT can be helpful in determining the size, location, local involvement and distant spread. Magnetic resonance imaging (MRI) provides similarly useful information as CT, but yields better visualisation of the tumour. Fine needle aspirate (FNA) cytology is not often helpful because the tissue architectural information required is not obtainable from cytological specimen . The only gold standard diagnostic investigation is histology of either biopsy or excised specimen.
Surgical excision has remained the mainstay of treatment. Although benign, large and incompletely excised lesions are capable of recurrence; malignant change is exceedingly rare [3, 10]. This patient will require a prolonged period of surveillance due to the large size of the tumour and the uncertainty of complete excision.
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