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Aggressive dissemination of central nervous system hemangioblastoma without association with von Hippel-Lindau disease: A case report and literature review.
Surg Neurol Int
August 2022
Department of Neurosurgery, Nova Lima, Minas Gerais, Brazil.
Background: Hemangioblastomas (HBs) typically present with benign behavior and are most commonly found in the posterior fossa. Multiple central nervous system (CNS) HBs are usually associated with von Hippel-Lindau disease, and leptomeningeal dissemination of sporadic HBs is extremely rare. A review of the literature identified 30 cases of leptomeningeal dissemination of sporadic HBs previously published in the literature.
View Article and Find Full Text PDFOvarian steroid cell tumor associated with von Hippel-Lindau syndrome: a report of two cases and literature review.
Int J Clin Exp Pathol
August 2022
Department of Pathology, Temple University Hospital, Temple University Philadelphia, PA, USA.
Steroid cell tumor (SCT) is a rare sex cord-stromal tumor accounting for only 0.1% of ovarian tumors. Steroid cell tumor, not otherwise specified (SCT, NOS) is of uncertain lineage and is the most common among the three subtypes of SCT.
View Article and Find Full Text PDFSpinal leptomeningeal hemangioblastomatosis occurring without craniospinal surgery in von Hippel-Lindau disease.
BMJ Case Rep
August 2022
Neurosurgery, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico.
Hemangioblastomatosis represents an unusual and malignant leptomeningeal dissemination of hemangioblastoma (HB). It has been reported in patients with sporadic HB or von Hippel-Lindau (VHL) disease. Hemangioblastomatosis had been reported following resection of a primary HB lesion in all cases except one patient with a sporadic HB.
View Article and Find Full Text PDFRetinal capillary hemangioblastomatosis and renal tumor in Von Hippel-Lindau disease.
Am J Ophthalmol Case Rep
June 2020
Roski Eye Institute, Department of Ophthalmology, Keck School of Medicine, University of Southern California, 1450 San Pablo St, Los Angeles, CA, USA.
Hemangioblastomatosis-associated negative-pressure hydrocephalus managed with improvised shunt.
J Clin Neurosci
December 2018
National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA. Electronic address:
Low-pressure hydrocephalus (LPH) is a rare clinical diagnosis, characterized by neurologic decline and ventriculomegaly that persists despite normal to low intracranial pressure. LPH is typically managed by negative-pressure drainage via ventriculostomy, followed by low-resistance shunt insertion. We present the case of a middle-aged man with a history of hemangioblastomatosis who had spontaneous subarachnoid hemorrhage.
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