4.5 Article

Extraneural hemangioblastoma - A report of 5 cases

Journal

AMERICAN JOURNAL OF SURGICAL PATHOLOGY
Volume 31, Issue 10, Pages 1545-1551

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/PAS.0b013e3180457bfc

Keywords

capillary hemangioblastoma; von Hippel-Lindau disease

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Hemangioblastoma is a morphologically distinctive tumor that can occur sporadically or in association with von Hippel-Lindau disease, and which involves the central nervous system in the majority of the cases. Rare occurrences of hemangioblastoma in peripheral nerves and extraneural tissues have been reported. The histogenesis of this tumor remains uncertain. Various cell lineages such as vascular, glial, neural, fibrohistiocytic, and smooth muscle/myofibroblastic have been proposed for the so-called stromal cells, which are thought to represent the neoplastic component of these lesions. We report on 5 cases of hemangioblastoma arising in extraneural tissues. Two of the tumors were located in the presacral region, and one each in the maxilla, kidney, and adrenal glands. All 5 cases were morphologically indistinguishable from central nervous system hemangioblastorna. The existence of these cases suggests that the stromal cells of hemangioblastoma can demonstrate a variety of mature specific lineages, such as smooth muscle/ inyofibroblastic, or neuroendocrine, depending on the location and possibly the microenvironment.

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