Korean J Urol.  2012 Nov;53(11):810-812.

Cavernous Hemangiolymphangioma of the Testis without Cutaneous Hemangiomatosis in an Elderly Patient

Affiliations
  • 1Department of Urology, Chonbuk National University Medical School, Jeonju, Korea. hjkim@jbnu.ac.kr
  • 2Department of Anesthesiology, Chonbuk National University Medical School, Jeonju, Korea.

Abstract

Hemangiolymphangioma is an extremely rare malformation of both the lymphatic and blood vessels. To date, however, there are no reports in the literature of a hemangiolymphangioma of the testis. An 84-year-old man visited our hospital for investigation of a 1-month episode of a rapidly growing mass in his right scrotum. Scrotal ultrasonography revealed a multilobulated mass with septation in the testis. Testicular tumor markers were within the normal limit. Radical orchiectomy was performed. At surgery, a red, wide-based, nodular tumor was found on the testis. Histological examination of the resected specimen showed it to be a cavernous hemangiolymphangioma. Here we report this first case of a cavernous hemangiolymphangioma of the testis without cutaneous hemangiomatosis in an elderly patient.

Keyword

Hemangioma; Lymphangioma; Testis

MeSH Terms

Aged
Aged, 80 and over
Blood Vessels
Caves
Hemangioma
Humans
Lymphangioma
Orchiectomy
Scrotum
Testis
Biomarkers, Tumor

Figure

  • FIG. 1 (A) Scrotum ultrasonography showing a multilobulated mass with septation in the testis. (B) Low blood flow was seen on color Doppler ultrasonography.

  • FIG. 2 Gross photograph of the testis after right radical orchiectomy. The testis was diffusely thickened and showed dilated blood vessels filled with blood.

  • FIG. 3 Histopathological features of the hemangiolymphangioma showing both hemangiomatous and lymphangiomatous components (H&E, ×100).


Reference

1. Donnelly LF, Adams DM, Bisset GS 3rd. Vascular malformations and hemangiomas: a practical approach in a multidisciplinary clinic. AJR Am J Roentgenol. 2000. 174:597–608.
2. Giacalone PL, Boulot P, Marty M, Deschamps F, Laffargue F, Viala JL. Fetal hemangiolymphangioma: a case report. Fetal Diagn Ther. 1993. 8:338–340.
3. Paladini D, Lamberti A, Teodoro A, Liguori M, D'Armiento M, Capuano P, et al. Prenatal diagnosis and hemodynamic evaluation of Klippel-Trenaunay-Weber syndrome. Ultrasound Obstet Gynecol. 1998. 12:215–217.
4. Tseng JJ, Chou MM, Ho ES. Fetal axillary hemangiolymphangioma with secondary intralesional bleeding: serial ultrasound findings. Ultrasound Obstet Gynecol. 2002. 19:403–406.
5. Vilanova JC, Barcelo J, Smirniotopoulos JG, Perez-Andres R, Villalon M, Miro J, et al. Hemangioma from head to toe: MR imaging with pathologic correlation. Radiographics. 2004. 24:367–385.
6. Cannard L, Lemelle JL, Gaconnet E, Champigneulle J, Mainard L, Claudon M. Dynamic MR imaging of bladder haemangioma. Pediatr Radiol. 2001. 31:882–885.
7. Engel JD, Kuzel TM, Moceanu MC, Oefelein MG, Schaeffer AJ. Angiosarcoma of the bladder: a review. Urology. 1998. 52:778–784.
8. Park JS, Chung DY, Kim SJ, Kim YS, Lee EJ, Park KH. Hemangioma of scrotum: a report of 3 cases. Korean J Urol. 1997. 38:885–888.
9. Loberant N, Chernihovski A, Goldfeld M, Sweed Y, Vais M, Tzilman B, et al. Role of Doppler sonography in the diagnosis of cystic lymphangioma of the scrotum. J Clin Ultrasound. 2002. 30:384–387.
10. Hamada Y, Yagi K, Tanano A, Kato Y, Takada K, Sato M, et al. Cystic lymphangioma of the scrotum. Pediatr Surg Int. 1998. 13:442–444.
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