Angioleiomyoma of urethra: A case report.

Urethral neoplasms, in particular benign mesenchymal tumors are exceedingly rare. To our knowledge only less than 5 cases of primary urethral angioleiomyomas are reported in literature mostly in females. Angioleiomyomas are benign smooth muscle tumors that are commonly seen in subcutaneous location of the extremities. Herein, we present a rare case of primary angioleiomyoma of urethra in a 72 years old male who presented with hematuria.

Rawan Amir: writing the manuscript. Salwa Sheikh: reviewer.

Not applicable.

Urethral polypoid lesions most commonly represent reactive inflammatory conditions. Primary urethral neoplasms are extremely rare. Most urethral lesions encompass urethral caruncle, diverticulum, mucosal prolapse, skene duct cyst/abscess, cowper gland duct cyst, fibroepithelial polyp, and prostatic-type poly. Rarely malakoplakia, endometriosis, and amyloidosis can be seen involving the urethral location. Urethral neoplasms, in particular benign mesenchymal tumors, are exceedingly rarely reported [1] . Marshall et al. reported a study of 394 lesions of female urethra revealing 372 benign lesions and only 22 malignant tumors. Caruncle was found to be the most commonly encountered lesion accounting for 96% and no leiomyoma or angioleiomyoma was reported in that study. Grabstaldt reported 96 urethral tumors again with not a single case of angioleiomyoma [2] . Subsequently, few leiomyomas were reported in literature with only rare cases of angioleiomyomas that arose from urethra [3–7] . Most of these angioleiomyomas were associated with obstructive symptoms as is the case with many other urethral lesions, however our patient presented only with gross hematuria and no symptoms of obstruction. Angioleiomyomas are common deep dermal, or subcutaneous benign, well-circumscribed smooth muscle tumors that originate from the walls of blood vessels in particular veins. Although the neoplasm can affect any age, it is commonly seen in adults between the age of 30 and 60 years of age. There is mild overall male predominance, however, larger studies show that there is female predominance when angioleiomyomas are seen involving lower extremities and male predominance in the head and neck region and upper extremities. 60% of the lesions occur in lower extremities below the thighs. Typically, the lesion presents as a solitary, small (less than 2 cm), slow growing, nodule affecting the extremities, and is often painful or tender on compression [8,9] . Only rare cases have been reported in literature that arise in urethral location. To our knowledge, less than five cases have been reported thus far that are mostly reported in females. Grossly these lesions are sharply circumscribed white rubbery nodules that are mostly 1–2 cm in size. Histologically, these are mostly round encapsulated lesions that are composed of many blood vessels of variably thickened walls that are surrounded by interlacing fascicles and bundles of uniform spindled cell. There may be areas of myxoid change, thrombosis, lipomatous metaplasia, or dystrophic calcifications. Rarely prominent nuclear palisading mimicking Verocay bodies is seen. Occasional cases may exhibit epithelioid changes of the cells and few cells with enlarged hyperchromatic nuclei, however, no increase in mitotic activity is seen in these cases. Such atypia without mitotic activity is considered secondary to degenerative or reactive changes and does not indicate malignancy. Lipomatous angioleiomyomas are sometimes erroneously called “angiomyolipomas”. True angiomyolipmas belong to the family of Perivascular epithelioid cell tumor (PEComas), however, angioleiomyomas are not related to PEComas and do not show the characteristic HMB-45 positive staining of PEComas. Three histologic variants have been recognized; the most common one being “capillary or solid” type representing approximately 67% of cases. Other variants include “venous” and “cavernous” types. Identification of these histologic variants is important for pathologists to be able to identify them and recognize them as variants of the same benign entity, however, has no clinical significance [10] . Immunohistochemistry shows cells to be positive for smooth muscle actin, calponin, and h-caldesmin. In addition, there is variable positive staining with desmin. Cytogenetic studies show chromosomal imbalances, with most consistent finding being recurrent losses in chromosome 22q11 [11] . Surgical excision is the recommended treatment for any urethral lesion mainly to identify the lesion histologically, and to distinguish reactive from neoplastic, and benign from malignant tumors. Examples include smooth muscle tumors to differentiate benign leiomyoma from leiomyosarcoma based on the number of mitotic figures and benign versus malignant urothelial neoplasms based on architectural and cytologic features. Recurrence of angioleiomyoma after simple excision is extremely rare and malignant transformation has not been convincingly documented or reported in literature.

In conclusion, we herein, report a case of a primary angioleiomyoma arising from a rarely encountered location, urethra, in a male patient who presented with only gross hematuria. Angioleiomyomas are benign smooth muscle neoplasms of vessel walls that are commonly seen in subcutaneous and deep dermal tissue of extremities. Only rare cases are reported to arise from other sites with only less than 5 cases reported in literature involving urethra.

A 72 year old male who is a known case of diabetes mellitus presented with gross hematuria of two day duration. There was no history of obstructive symptoms. His physical examination was unremarkable apart from markedly enlarged prostate that was identified on rectal examination. Repeated urine cytology showed few atypical cells. His laboratory data showed normal hemogram and electrolytes. Ultrasound showed normal kidneys and urinary bladder. Retrograde pyelogram was normal. Due to the persistent gross hematuria and passage of blood clots and presence of atypical cells in urine, clinical decision was made to do cystoscopy and at the same time do transurethral resection of prostate (TURP) since the patient had a markedly enlarged prostate. Cystoscopy showed an incidental urethral polypoid lesion that was excised in addition to random biopsies that were taken from the urinary bladder. Pathological examination showed no significant histopathologic findings in the bladder biopsies. The prostatic tissue exhibited benign prostatic hyperplasia. The prostatic urethral polyp showed a well circumscribed nodule exhibiting scattered thick walled blood vessels that were surrounded by spindle cell proliferation ( Fig. 1 ). The cells were elongated, had eosinophilic cytoplasm, bland appearing nuclei, and lacked any cytologic atypia or increased mitotic activity ( Fig. 2 A). In addition, there was underlying mild chronic inflammation. The spindle cell proliferation and the smooth muscle walls of the blood vessels were strongly positive for Actin ( Fig. 2 B). The histologic features were consistent with an angioleiomyoma. The patient had an uneventful postoperative course and 12 years later he had no recurrence of hematuria, atypical cells in urine, or evidence of recurrent urethral lesion.