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- W2014080767 abstract "Case Reports1 July 1961Pheochromocytoma and Meningioma of the Foramen MagnumARNOLD GREENHOUSE, M.D.ARNOLD GREENHOUSE, M.D.Search for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-55-1-124 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptThe relationship between pheochromocytoma and other tumors of neural origin, particularly neurofibromas, has been emphasized in recent years. The appreciation of such an association may be of diagnostic value. The present communication concerns the appearance of a meningioma in a patient from whom a pheochromocytoma had previously been removed, and may indicate a further link in a group of related tumors.CASE REPORTA 58-year-old white male was initially admitted to the Denver Veterans Administration Hospital in July, 1955, complaining of weakness and unsteadiness of the legs and numbness of the hands. He had been well until 1947, when he...References1. SYMONDSMEADOWS CPSP: Compression of the spinal cord in the neighborhood of the foramen magnum. Brain 60: 52, 1937. CrossrefGoogle Scholar2. CUSHINGEISENHARDT HL: Meningiomas: Their Classification, Regional Behavior, Life History and Surgical End Results, Charles C Thomas, Springfield, Ill., 1938, pp. 87-91 and 169-180. Google Scholar3. SUZUKI S: Über zwei Tumoren aus Nebennierenmarkgewebe. Klin. Wschr. 47: 1623, 1910. Google Scholar4. KAWASHIMA K: Über einen Fall von multiplen Hautfibromen mit Nebennierengeschwulst. Virchow. Arch. Path. 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CrossrefMedlineGoogle Scholar12. MANDEVILLESAHYOUN FBPF: Benign and malignant pheochromocytomas with necropsies: benign case with neurofibromatosis and cavernous hemangioma of the 4th ventricle; malignant case with widespread metastases and bronchogenic carcinoma. J. Urol. 62: 93, 1949. CrossrefMedlineGoogle Scholar13. DAVISHULLVARDELL FWJGJC: Pheochromocytoma with neurofibromatosis. Amer. J. Med. 8: 131, 1950. CrossrefMedlineGoogle Scholar14. KOONCEPOLLACKGLASSY DHBEFJ: Bilateral pheochromocytoma associated with neurofibromatosis. Amer. Heart J. 44: 901, 1952. CrossrefMedlineGoogle Scholar15. GLUSHIENMANSUYLITTMAN ASMMDS: Pheochromocytoma; its relationship to the neurocutaneous syndromes. Amer. J. Med. 14: 318, 1953. CrossrefMedlineGoogle Scholar16. RUSHEDE J: Pheochromocytoma associated with neurofibromatosis. Acta Psychiat. Scand. 30: 749, 1955. CrossrefGoogle Scholar17. KNOXSLESSOR JA: Pheochromocytoma with neurofibromatosis: adrenolytic effects of phentolamine and chlorpromazine. Lancet 1: 790, 1955. CrossrefGoogle Scholar18. MORRISONSCHULEMANBOREN BJHJS: Neurofibromatosis with symptoms secondary to pheochromocytoma. Neurology 6: 305, 1956. CrossrefMedlineGoogle Scholar19. BOLDTFLEXNERORTNER MHMAB: Pheochromocytoma associated with painless myocardial infarction. Ann. Intern. Med. 46: 1165, 1957. LinkGoogle Scholar20. LOPEZ JF: Pheochromocytoma of the adrenal gland with granulosa cell tumor and neurofibromatosis: report of a case with fatal outcome following abdominal aortography. Ann. Intern. Med. 48: 187, 1958. LinkGoogle Scholar21. HEALEYMIKALETOS FHCJ: Pheochromocytoma with neurofibromatosis. Report of a case. New Engl. J. Med. 258: 540, 1958. CrossrefMedlineGoogle Scholar22. CHAPMANKEMPTALLIAFERRO RCVEI: Pheochromocytoma associated with multiple neurofibromatosis and intracranial hemangioma. Amer. J. Med. 26: 883, 1959. CrossrefMedlineGoogle Scholar23. CROWESCHULLNEAL FWWJJV: A Clinical, Pathological and Genetic Study of Neurofibromatosis. Charles C Thomas, Springfield, Ill., 1956, pp. 38-39 and 42-43. Google Scholar24. ZULCH KJ: Brain Tumors. Their Biology and Pathology. Springer Publishing Co., New York, 1957, pp. 43-45. Google Scholar25. RUSSELLRUBENSTEIN DSLJ: Pathology of Tumours of the Nervous System. The Williams & Wilkins Co., Baltimore, 1959, pp. 31-37. Google Scholar26. WAHL HR: Neuroblastoma with study of a case illustrating the three types. J. Med. Res. 30: 205, 1914. MedlineGoogle Scholar27. LEWISGESCHICHTER DCF: Tumors of the sympathetic nervous system: neuroblastoma, paraganglioma and ganglioneuroma. Arch. Surg. 28: 16, 1934. CrossrefGoogle Scholar28. WAHLCRAIG HRPE: Multiple tumors of the sympathetic nervous system: report of a case showing distinct ganglioneuroma, neuroblastoma and a cystic calcifying ganglioneuroblastoma. Amer. J. Path. 14: 797, 1938. MedlineGoogle Scholar29. WAHLROBINSON HRD: Neuroblastoma of the mediastinum with pheochromoblastomatous elements. Arch. Path. 35: 571, 1943. Google Scholar30. FERNANDOCOORAYTHANABALASUNDRAM PBGHRS: Adrenal pheochromocytoma with neuroblastomatous elements. Report of a case with autopsy. Arch. Path. 52: 182, 1951. Google Scholar31. TAMURALAWRENCE PHLT: Multiple tumors of the sympathetic system. A report of a case of malignant schwannoma associated with functioning malignant pheochromocytoma. Cancer 9: 293, 1956. CrossrefMedlineGoogle Scholar This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAffiliations: Denver, ColoradoReceived for publication June 21, 1960.From the Division of Neurology, Veterans Administration Hospital; and the University of Colorado Medical Center, Denver, Colo.Requests for reprints should be addressed to Arnold Greenhouse, M.D., Veterans Administration Hospital, 1055 Clermont St., Denver 20, Colo. PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics Cited byA Patient with an Extra-adrenal Pheochromocytoma and Germ-line SDHB Mutation Accompanied by an Atypical MeningiomaRaumbeengende Prozesse im Spinalkanal (einschließlich Angiome und Parasiten)A FUNCTIONING MALIGNANT PHAEOCHROMOCYTOMA OCCURRING IN A PATIENT WITH NEUROFIBROMATOSISMultiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndromeA Genetical View of Cardiovascular DiseaseBibliographyFamilial Pheochromocytoma with Ependymoma of the Spinal Cord 1 July 1961Volume 55, Issue 1Page: 124-127KeywordsNeurologyPheochromocytomaScleroderma Issue Published: 1 July 1961 PDF downloadLoading ..." @default.
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