Dabska tumor (Endovascular papillary angioendothelioma) of testis: a case report with brief review of literature
© ; licensee BioMed Central Ltd. 2006
Received: 13 July 2006
Accepted: 22 July 2006
Published: 22 July 2006
The Dabska tumor also known as Endovascular papillary angioendothelioma is a rare type of hemangioendothelioma characterized by intraluminal papillary endothelial structures. Most of these are superficial in location but occurrence in deeper tissues is also known. We describe case report of testicular Dabska tumor in a child presenting as inguinal hernia. To the best of our knowledge this is the first case report describing the occurrence of this rare entity in testis.
The Dabska tumor is a rare, low-grade angiosarcoma that often affects the skin and subcutaneous tissues of children . Microscopically, it is characterized by anastomosing vascular channels, some of which contain papillary projections or tuft-like structures sometimes resembling renal glomeruli. These vascular channels as well as papillations are lined by cuboidal endothelial cells and are often flanked by dense hyalinized zones containing lymphocytes. The hyalinized material is thought to represent the basement membrane material possibly synthesized by tumor cells . Although rare cases of Dabska tumors have been reported in deeper locations, there is no case report describing the occurrence of this entity in testis. We therefore report first case of Dabska tumor arising in testis of a 1 year, 10 month old child who first presented as inguinal hernia.
A 1 year 10 month old male child was referred to our pediatric surgery department for pain and tenderness in a scrotal swelling for past 2 days. The swelling was diagnosed as non-obstructive inguinal hernia at the referral centre at 2 months of age. As it was not progressing the parents were advised to wait till the age of one year. There was no history of any trauma to genitalia. On examination the scrotum was swollen on left side and left testis was not palpable separately. The right testis was normally palpable in scrotal sac. Ultrasonographic examination of the swelling showed a markedly enlarged testis with a heterogenous echotexture. A possibility of testicular tumor was suggested and Fine Needle Aspiration Cytology (FNAC)/biopsy were advised. The FNAC showed few clusters of spindle cells and some cells with prominent nucleoli and vacuolated cytoplasm. However no definite opinion was given. A biopsy was also done which was reported as infarction of testis with extensive vascular proliferation. Subsequently a high left inguinal orchidectomy was carried out. Intraoperatively the hernial sac contained clear fluid and no bowel loops were seen. The specimen was sent for histopathology.
The Dabska tumor was first described in 1969 by Maria Dabska in skin and subcutaneous tissues in children and named as malignant endovascular papillary angioendothelioma. She described 6 cases in her series . Since then approximately 30 cases have been described in the literature. Of these 18 were children and 12 were adults. The age of the patients ranged from birth to 83 years and there was no sex predilection [4, 5]. Besides skin and subcutaneous tissue, the tumor has been described in other deeper locations like spleen , soft tissues , bone , and tongue . Generally it presents as a slow-growing, painless, usually intradermal nodule that grows to 2–3 cm in diameter. In our case this tumor presented as inguinal hernia and after surgery was found to be a solid mass with cystic change. This kind of presentation has not been described in any of the previous studies. At low power, Dabska tumor appears similar to cavernous lymphangiomas. The cuboidal or hobnail endothelial cells lining the vascular structures are characterized by a high nuclear cytoplasmic ratio and an apically placed nucleus that produces a surface bulge, accounting for the term "hobnail" or "matchstick" . Individual endothelial cells range from cuboidal to tall and cylindrical with vacuolated cytoplasm and hyperchromatic eccentric nuclei on their luminal border. Mitotic figures may be seen, as in our case. Many intraluminal lymphocytes may also be evident, often attached to the endothelial cells. All these features were noted in our case. Immunohistochemically the tumor cells are positive for Von-Willebrand factor, CD31, CD34 and vascular endothelial growth factor receptor-3 (VEGFR-3). The staining for CD34 and VEGFR-3 is most intense out of these . In the present case strong positivity for CD34 immunostaining was observed in tumor cells. Ultrastructural examination demonstrates tumor cells with irregular nuclei, abundant perinuclear cytoplasmic filaments, and many pinocytotic vesicles. Weibel-Palade bodies may be evident. The hyaline globules consist of electron-dense basement membrane material .
Along with a closely related tumor, the retiform hemangioendothelioma it comes under the category of Hobnail hemangioendothelioma, a subtype of hemangioendothelioma. Pathophysiologcally it has been viewed as a distinct intralymphatic neoplasia and renamed as papillary intralymphatic angioendothelioma . These tumors are known to occur in previously existing benign vascular lesions like cavernous hemangiomas . In our case no cavernous hemangioma like areas could be found even after extensive sampling
Orchidectomy is the treatment of choice. Prognostically these tumors are low grade lesions with a capacity to extend to regional lymph nodes . Three of the original 6 cases were locally aggressive, with tumor invasion into deeper structures, including bone, musculature, fascia, and/or tendons. One of Dabska's original 6 Dabska tumor patients ultimately died of widespread pulmonary metastases . Therefore, Dabska tumor though believed to have a favorable prognosis, can be locally invasive with a potential to metastasize. In the present case there was no evidence of any nodal involvement or distant metastasis and the child was doing well on last follow up after 1 year of surgery.
Our case describes the first occurrence of this entity in testis with an unusual presentation in the form of inguinal hernia. It also highlights the difficulty in diagnosing such tumors on FNAC or small biopsy specimens as it was mistaken for an infarct on biopsy.
- Sharon Weiss, John Goldblum: Hemangioendothelioma: Vascular tumors of intermediate malignancy. Soft tissue tumors. Edited by: Enzinger FM, Weiss SW. 2001, St. Louis: Mosby, 891-915. 4Google Scholar
- Patterson K, Chandra RS: Malignant endovascular papillary angioendothelioma: a cutaneous borderline tumor. Arch Pathol Lab Med. 1985, 109: 671-3.PubMedGoogle Scholar
- Dabska M: Malignant endovascular papillary angioendothelioma of skin in childhood. Cancer. 1969, 24: 503-10. 10.1002/1097-0142(196909)24:3<503::AID-CNCR2820240311>3.0.CO;2-L.View ArticlePubMedGoogle Scholar
- Brazzelli V, Baldini F, Vassallo C, Borghini F, Chiesa MG, Rosso R, Borroni G: Reactive angioendotheliomatosis in an infant. Am J Dermatopathol. 1999, 21 (1): 42-5. 10.1097/00000372-199902000-00010.View ArticlePubMedGoogle Scholar
- Yamada A, Uematsu K, Yasoshima H, Sakurai K, Hori K, Ohya M, Ohkubo E, Ogasawara H: Endovascular papillary angioendothelioma (Dabska tumor) in an elderly woman. Pathol Int. 1998, 48 (2): 164-7.View ArticlePubMedGoogle Scholar
- Katz JA, Mahoney DH, Shukla LW, Smith CW, Gresik MV, Hawkins HK: Endovascular papillary angioendothelioma in spleen. Pediatr Pathol. 1988, 8: 185-93.View ArticlePubMedGoogle Scholar
- Argani P, Athanasian E: Malignant endovascular papillary angioendothelioma (Dabska tumor) arising within deep intramuscular hemangioma. Arch Pathol Lab Med. 1997, 121: 992-5.PubMedGoogle Scholar
- McCarthy EF, Lietman S, Argani P, Frassica FJ: Endovascular papillary angioendothelioma (Dabska tumor) of bone. Skeletal Radiol. 1999, 28 (2): 100-3. 10.1007/s002560050482.View ArticlePubMedGoogle Scholar
- Takaoka K, Sakurai K, Noguchi K, Hashitani S, Urade M: Endovascular papillary angioendothelioma (Dabska tumor) of the tongue: report of a case. J Oral Pathol Med. 2003, 32 (8): 492-5. 10.1034/j.1600-0714.2003.00120.x.View ArticlePubMedGoogle Scholar
- Fanburg-Smith JC, Michal M, Partanen TA, Alitalo K, Miettinen M: Papillary Intralymphatic Angioendothelioma (PILA): A Report of Twelve Cases of a Distinctive Vascular Tumor with Phenotypic Features of Lymphatic Vessels. Am J Surg Pothol. 1999, 23 (9): 1004-10. 10.1097/00000478-199909000-00002.View ArticleGoogle Scholar
- Enzinger FM, Weiss SW, eds: Soft Tissue Tumors. 1995, St. Louis Mo: Mosby, 637-40. 3Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.