Elsevier

Human Pathology

Volume 7, Issue 1, January 1976, Pages 61-82
Human Pathology

Hemangiopericytoma: An analysis of 106 cases*

https://doi.org/10.1016/S0046-8177(76)80006-8Get rights and content

Abstract

A series of 106 cases of hemangiopericytoma was analyzed. The neoplasms occurred principally in adults (median age, 45 years), were deep seated, and were most common in the thigh (27 cases) and the pelvic retroperitoneum (26 cases). A painless mass was the first symptom in 96 of the patients. The median size of the excised tumors was 6.5 cm. Surgical removal of the tumor was often complicated by hemorrhage because of marked dilatation of the vascular bed in the vicinity of the neoplasm, probably as the result of rapid exchange of blood from the arterial to the venous circulation within the tumor. Microscopically, benign and malignant forms could be distinguished. The latter were characterized by increased cellularity, prominent mitotic activity, and foci of necrosis or hemorrhage. Follow-up information was obtained in 93 cases. Seventy-one of the 93 patients were living (two with recurrence and four with metastasis), and 22 had died (13 as the result of recurrence or metastasis and nine from unrelated causes). Recurrence preceded metastasis in more than two-thirds of the patients with evidence of metastasis. The 10 year survival rate was 70 per cent. The morphologic differences from other mesenchymal tumors showing a hemangiopericytoma-like vascular pattern are discussed, and the close resemblance of hemangiopericytoma to richly vascular forms of fibrous histiocytomas and synovial sarcoma is emphasized. Congenital or infantile hemangiopericytoma is described as a separate entity having a distinctive microscopic pattern and behavior.

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      Hemangiopericytoma is a rare, vascular tumor originating from the pericytes surrounding capillaries.1 They present as red or brown painless masses in the fifth decade of life and are usually encountered in ophthalmic pathology as orbital neoplasms.1 Its occurrence as a solitary conjunctival mass is very rare, with only four other cases reported in the literature.2–4

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    *

    The opinions or assertions contained herein are the private views of the authors and are not to be construed as being official or as reflecting the views of the Department of the Army or the Department of Defense.

    Chief, Soft, Tissue Division, Armed Forces Institute of Pathology, Washington, D.C.

    Chief, Department of Pathology, Veterans Administration Hospital, Washington, D.C.

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